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<dc:title><![CDATA[Isolated Intracranial Rosai-Dorfman Disease in a Child [LETTERS]]]></dc:title>
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<title><![CDATA[Lymphomatous Meningosis Diagnosed with [18F]-Fluorodeoxyglucose-Positron-Emission Tomography/CT [LETTERS]]]></title>
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<dc:title><![CDATA[Lymphomatous Meningosis Diagnosed with [18F]-Fluorodeoxyglucose-Positron-Emission Tomography/CT [LETTERS]]]></dc:title>
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<title><![CDATA[PET in the Evaluation of Alzheimer Disease and Related Disorders [BOOK REVIEWS]]]></title>
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<dc:title><![CDATA[The Neurological Manifestations of Pediatric Infectious Diseases and Immunodeficiency Syndromes [BOOK REVIEWS]]]></dc:title>
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<title><![CDATA[Emergency Radiology: The Requisites and Emergency Radiology: Case Review Series [BOOK REVIEWS]]]></title>
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<dc:title><![CDATA[Emergency Radiology: The Requisites and Emergency Radiology: Case Review Series [BOOK REVIEWS]]]></dc:title>
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<title><![CDATA[Balloon Kyphoplasty [BOOK REVIEWS]]]></title>
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<title><![CDATA[EXPERT ddx Head and Neck [BOOK REVIEWS]]]></title>
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<title><![CDATA[Meningiomas: Diagnosis, Treatment, and Outcome [BOOK REVIEWS]]]></title>
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<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/E158?rss=1">
<title><![CDATA[Pediatric Radiology: The Requisites [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/E158?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Blickman, J.G., Parker, B.R., Barnes, P.D.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1764</dc:identifier>
<dc:title><![CDATA[Pediatric Radiology: The Requisites [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E158</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>E158</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1807?rss=1">
<title><![CDATA[Preservation of Knowledge, Part 2: Digital Archives [PERSPECTIVES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1807?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Castillo, M.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1656</dc:identifier>
<dc:title><![CDATA[Preservation of Knowledge, Part 2: Digital Archives [PERSPECTIVES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1808</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1807</prism:startingPage>
<prism:section>PERSPECTIVES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1808?rss=1">
<title><![CDATA[Randomized Vertebroplasty Trials: Bad News or Sham News? [EDITORIALS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1808?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Noonan, P.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1875</dc:identifier>
<dc:title><![CDATA[Randomized Vertebroplasty Trials: Bad News or Sham News? [EDITORIALS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1809</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1808</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1809?rss=1">
<title><![CDATA[Response to "Randomized Vertebroplasty Trials: Bad News or Sham News?" [EDITORIALS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1809?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Kallmes, D., Buchbinder, R., Jarvik, J., Heagerty, P., Comstock, B., Turner, J., Osborne, R.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1887</dc:identifier>
<dc:title><![CDATA[Response to "Randomized Vertebroplasty Trials: Bad News or Sham News?" [EDITORIALS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1810</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1809</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1811?rss=1">
<title><![CDATA[[18F] Fluorodeoxyglucose-Positron-Emission Tomography and MR Imaging Coregistration for Presurgical Evaluation of Medically Refractory Epilepsy [REVIEW ARTICLES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1811?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Epilepsy is a chronic disorder affecting approximately 1% of the population of the world. Approximately one third of patients with epilepsy remain refractory to medical therapy. For these patients, surgery is a curative option. In order for surgery to be considered, precise localization of the structural abnormality is needed. When MR imaging findings are normal, more sensitive techniques such as positron-emission tomography (PET) can help find the abnormality. Combining MR imaging and PET information increases the sensitivity of the presurgical evaluation. In this review, we discuss the clinical applications of coregistration of [<sup>18</sup>F] fluorodeoxyglucose (FDG)-PET with MR imaging for medically refractory epilepsy. Because FDG-PET/MR imaging coregistration has been a routine component of the presurgical evaluation for patients with epilepsy at our institution since 2004, we also included cases from our data base that exemplify the utility of this technology to obtain better postsurgical outcomes.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lee, K.K., Salamon, N.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1637</dc:identifier>
<dc:title><![CDATA[[18F] Fluorodeoxyglucose-Positron-Emission Tomography and MR Imaging Coregistration for Presurgical Evaluation of Medically Refractory Epilepsy [REVIEW ARTICLES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1816</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1811</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1817?rss=1">
<title><![CDATA[The Radiology of Referred Otalgia [REVIEW ARTICLES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1817?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Pain referred to the ear is a well-documented phenomenon, which can be due to a multitude of disease processes. With the recent and rapid progression of CT and MR imaging technology, radiologists have played an increasing role in solving this potentially difficult diagnostic dilemma. Essentially any pathology residing within the sensory net of cranial nerves V, VII, IX, and X and the upper cervical nerves C2 and C3 can potentially cause referred otalgia. This article will attempt to outline the various sensorineural pathways that dually innervate the ear and other sites within the head and neck, as well as discuss various disease processes that are known to result in referred otalgia.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Chen, R.C., Khorsandi, A.S., Shatzkes, D.R., Holliday, R.A.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1605</dc:identifier>
<dc:title><![CDATA[The Radiology of Referred Otalgia [REVIEW ARTICLES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1823</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1817</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1824?rss=1">
<title><![CDATA[A Proposed Methodology to Select Radioisotopes for Use in Radionuclide Therapy [METHODOLOGIC PERSPECTIVES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1824?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>The <I>American Journal of Neuroradiology</I> has played a seminal role in the history of vertebral augmentation (VA). Because VA is increasingly being included in the multidisciplinary management of malignant vertebral compression fractures (VCFs), combined therapeutic approaches that include strategies to treat metastatic disease along with the fracture have become appealing options for patients. To that end, we recently investigated the dosimetric feasibility of treating malignant VCFs with radionuclide therapy. The goal would be to provide local control of the systemic disease beyond the pain relief and structural support provided by polymethylmethacrylate cement. The purpose of this article is to propose a methodology for evaluating radionuclides for use in radiation therapy that takes into account a number of factors including radiation characteristics, biochemical effects, production capacity, and safety. The goal of such a methodology is to introduce a systematic approach to selecting radionuclides in designing treatment regimens and future investigations and also to stimulate discussion and experimentation involving new radionuclides that may provide more effective treatments than the current isotopes in widespread use.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Cuaron, J.J., Hirsch, J.A., Medich, D.C., Rosenstein, B.S., Martel, C.B., Hirsch, A.E.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1773</dc:identifier>
<dc:title><![CDATA[A Proposed Methodology to Select Radioisotopes for Use in Radionuclide Therapy [METHODOLOGIC PERSPECTIVES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1829</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1824</prism:startingPage>
<prism:section>METHODOLOGIC PERSPECTIVES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1830?rss=1">
<title><![CDATA[Subsequent Fracture after Percutaneous Vertebroplasty Can Be Predicted on Preoperative Multidetector Row CT [SPINE]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1830?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Subsequent fracture is often seen after percutaneous vertebroplasty. The purpose of this prospective study was to evaluate preoperative multidetector row CT (MDCT) for the prediction of subsequent fractures after vertebroplasty.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>This study included 26 consecutive patients (18 women and 8 men) with osteoporotic compression fractures (58 vertebrae). A 64-section MDCT with multiplanar reformation was obtained 1 day before the procedure. Subsequent MR imaging was used to evaluate new fractures at least 3 months after treatment on a routine basis or if there was recurrent pain. We used logistic regression analysis with MDCT findings and clinical data for statistical evaluation according to the location of new fractures.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Subsequent fractures were noted at 14 adjacent vertebrae (12.1%) in 13 patients and at 14 remote vertebrae in 6 patients (23.1%). Subsequent fractures in adjacent vertebrae tended to occur in small vertebrae before treatment (<I>P</I> &lt; .05). Steroid medication and low CT value in nonfractured vertebrae were associated with subsequent fractures in remote vertebrae (<I>P</I> &lt; .05). Further collapse of the treated vertebral bodies was noted in 10 patients (11 vertebrae [19.0%]) without specific findings (<I>P</I> &gt; .05).</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The small size of the treated vertebrae may relate to subsequent fractures in adjacent vertebrae. Steroid use and low CT value of nonfractured vertebrae on preoperative MDCT can be associated with subsequent fractures in remote vertebrae.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Hiwatashi, A., Yoshiura, T., Yamashita, K., Kamano, H., Dashjamts, T., Honda, H.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1722</dc:identifier>
<dc:title><![CDATA[Subsequent Fracture after Percutaneous Vertebroplasty Can Be Predicted on Preoperative Multidetector Row CT [SPINE]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1834</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1830</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1835?rss=1">
<title><![CDATA[Vertebroplasty: What Is Important and What Is Not [SPINE]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1835?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>It is important to try to clarify the methodology of vertebroplasty such as amount of cement needed, how many needles to use and the significance of cement extravasation. This prospective study evaluated the potential of vertebroplasty to increase the likelihood of an adjacent vertebral compression fracture (VCF) 1 year or less after vertebroplasty, the correlation between the cement volumes injected and pain relief, and the consequences of cement extravasation.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Pain relief and the incidence of a subsequent fracture of adjacent vertebrae 1 year or less after vertebroplasty were evaluated in 357 patients (660 vertebrae) of mean age 77.5 years with osteoporotic VCFs. The correlation between cement volume and pain relief was assessed with a Pearson correlation coefficient; factors potentially predictive of subsequent adjacent VCFs were explored by multiple logistic regression analysis.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Refracture of any vertebrae (adjacent or nonadjacent to the primary fracture) occurred in 18% of the patients 1 year or less after vertebroplasty. Refracture of adjacent vertebrae occurred 1 year or less after vertebroplasty in 12% of the patients. Neither cement volume nor extravasation of cement into the intravertebral disk was a significant predictor of adjacent VCFs. No correlation was found between cement volume and pain relief (<I>r</I> = &ndash;0.029). Extravasation of cement into the veins, soft tissue, or disk was observed in 33% of all of the treated VCFs and resulted in no complications.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The incidence of an adjacent VCF 1 year or less after vertebroplasty was comparable with that expected for untreated osteoporotic VCFs. Neither the volume of cement injected nor extravasation of cement into the intravertebral disk affected the likelihood of subsequent adjacent VCFs. Cement volume did not correlate with pain relief.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Al-Ali, F., Barrow, T., Luke, K.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1732</dc:identifier>
<dc:title><![CDATA[Vertebroplasty: What Is Important and What Is Not [SPINE]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1839</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1835</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1840?rss=1">
<title><![CDATA[Subminute Fat-Water-Separated Dual-Echo Automated Spine Survey Iterative Scan Technique [SPINE]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1840?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>We developed and tested an automated sub-minute 3D dual-echo MR imaging technique producing fat-water color-encoded labeled images of the entire spine. Twenty-one subjects were scanned with the 2-point Dixon technique utilizing 2 contiguous 21-22 second breath-hold sagittal acquisitions. Fourteen alternating subject scan sessions were achieved in 58 minutes. In all cases, fat-water separation was homogenous over the 70 cm FOV; in 2 lower stations fat/water assignments were reversed. Rapid automated fat-water decomposition spine screening is a promising technique.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Weiss, K.L., Richards, C.R., Sun, D., Weiss, J.L.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1619</dc:identifier>
<dc:title><![CDATA[Subminute Fat-Water-Separated Dual-Echo Automated Spine Survey Iterative Scan Technique [SPINE]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1846</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1840</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1847?rss=1">
<title><![CDATA[Spinal Epidural Lubricant Grease Collection Mimicking Traumatic Spinal Epidural Hematoma [SPINE]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1847?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>We report an unusual case of a patient with an epidural fluid collection with signal characteristics mimicking an epidural hematoma. The patient presented with myelopathy caused by thoracic spinal cord compression after a traumatic injury to the chest and back. The injury was caused by high-pressure injection of industrial-grade lubricant grease. This case demonstrates that cord compression can be caused by exogenous material in the setting of trauma that can mimic an acute epidural hematoma.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kalnins, A.U., Geryk, B., Olivero, W., Kim, T.A.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1670</dc:identifier>
<dc:title><![CDATA[Spinal Epidural Lubricant Grease Collection Mimicking Traumatic Spinal Epidural Hematoma [SPINE]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1849</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1847</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1850?rss=1">
<title><![CDATA[Brain Structural Variability due to Aging and Gender in Cognitively Healthy Elders: Results from the Sao Paulo Ageing and Health Study [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1850?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Several morphometric MR imaging studies have investigated age- and sex-related cerebral volume changes in healthy human brains, most often by using samples spanning several decades of life and linear correlation methods. This study aimed to map the normal pattern of regional age-related volumetric reductions specifically in the elderly population.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>One hundred thirty-two eligible individuals (67&ndash;75 years of age) were selected from a community-based sample recruited for the S&atilde;o Paulo Ageing and Health (SPAH) study, and a cross-sectional MR imaging investigation was performed concurrently with the second SPAH wave. We used voxel-based morphometry (VBM) to conduct a voxelwise search for significant linear correlations between gray matter (GM) volumes and age. In addition, region-of-interest masks were used to investigate whether the relationship between regional GM (rGM) volumes and age would be best predicted by a nonlinear model.</p>
</sec>
<sec><st>RESULTS:</st>
<p>VBM and region-of-interest analyses revealed selective foci of accelerated rGM loss exclusively in men, involving the temporal neocortex, prefrontal cortex, and medial temporal region. The only structure in which GM volumetric changes were best predicted by a nonlinear model was the left parahippocampal gyrus.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The variable patterns of age-related GM loss across separate neocortical and temporolimbic regions highlight the complexity of degenerative processes that affect the healthy human brain across the life span. The detection of age-related limbic GM decrease in men supports the view that atrophy in such regions should be seen as compatible with normal aging.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Curiati, P.K., Tamashiro, J.H., Squarzoni, P., Duran, F.L.S., Santos, L.C., Wajngarten, M., Leite, C.C., Vallada, H., Menezes, P.R., Scazufca, M., Busatto, G.F., Alves, T.C.T.F.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1727</dc:identifier>
<dc:title><![CDATA[Brain Structural Variability due to Aging and Gender in Cognitively Healthy Elders: Results from the Sao Paulo Ageing and Health Study [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1856</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1850</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1857?rss=1">
<title><![CDATA[The Effect of Exercise on the Cerebral Vasculature of Healthy Aged Subjects as Visualized by MR Angiography [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1857?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Prior studies suggest that aerobic exercise may reduce both the brain atrophy and the decline in fractional anisotropy observed with advancing age. It is reasonable to hypothesize that exercise-induced changes to the vasculature may underlie these anatomic differences. The purpose of this blinded study was to compare high-activity and low-activity healthy elderly volunteers for differences in the cerebrovasculature as calculated from vessels extracted from noninvasive MR angiograms (MRAs).</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Fourteen healthy elderly subjects underwent MRA. Seven subjects reported a high level of aerobic activity (64 &plusmn; 5 years of age; 5 men, 2 women) and 7, a low activity level (68 &plusmn; 6 years of age; 5 women, 2 men). Following vessel segmentation from MRA by an individual blinded to subject activity level, quantitative measures of vessel number, radius, and tortuosity were calculated and histogram analysis of vessel number and radius was performed.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Aerobically active subjects exhibited statistically significant reductions in vessel tortuosity and an increased number of small vessels compared with less active subjects.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Aerobic activity in elderly subjects is associated with lower vessel tortuosity values and an increase in the number of small-caliber vessels. It is possible that an aerobic exercise program may contribute to healthy brain aging. MRA offers a noninvasive approach to visualizing the cerebral vasculature and may prove useful in future longitudinal investigations.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Bullitt, E., Rahman, F.N., Smith, J.K., Kim, E., Zeng, D., Katz, L.M., Marks, B.L.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1695</dc:identifier>
<dc:title><![CDATA[The Effect of Exercise on the Cerebral Vasculature of Healthy Aged Subjects as Visualized by MR Angiography [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1863</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1857</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1864?rss=1">
<title><![CDATA[Recombinant Tissue Plasminogen Activator Increases Blood-Brain Barrier Disruption in Acute Ischemic Stroke: An MR Imaging Permeability Study [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1864?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Although thrombolytic therapy (recombinant tissue plasminogen activator [rtPA]) represents an important step forward in acute ischemic stroke (AIS) management, there is a clear need to identify high-risk patients. The purpose of this study was to investigate the role of quantitative permeability (KPS) MR imaging in patients with AIS treated with and without rtPA. We hypothesized that rtPA would increase KPS and that KPS MR imaging can be used to predict the risk of hemorrhagic transformation (HT).</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Thirty-six patients with AIS were examined within a mean of 3.6 hours of documented symptom onset. KPS MR imaging was performed as part of our AIS protocol. KPS coefficients in the stroke lesion were estimated for all patients, and the relationship between KPS and both HT and rtPA was investigated by using Student <I>t</I> tests. Receiver operating characteristic (ROC) curves were computed for predicting HT from KPS.</p>
</sec>
<sec><st>RESULTS:</st>
<p>The occurrence rate of HT for patients who received rtPA and those who did not was 43% and 37%, respectively. Assessment of KPS in the lesion revealed significant differences between those who hemorrhaged and those who did not (<I>P</I> &lt; .0001) as well as between rtPA-treated and untreated patients (<I>P</I> = .008). ROC analysis indicated a KPS threshold of 0.67 mL/100 g/min, with a sensitivity of 92% and a specificity of 78%.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The results of this study indicate that KPS is able to identify patients at higher risk of HT and may allow use of physiologic imaging rather than time from onset of symptoms to guide treatment decision.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kassner, A., Roberts, T.P.L., Moran, B., Silver, F.L., Mikulis, D.J.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1774</dc:identifier>
<dc:title><![CDATA[Recombinant Tissue Plasminogen Activator Increases Blood-Brain Barrier Disruption in Acute Ischemic Stroke: An MR Imaging Permeability Study [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1869</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1864</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1870?rss=1">
<title><![CDATA[Association of White Matter Hyperintensity Measurements on Brain MR Imaging with Cognitive Status, Medial Temporal Atrophy, and Cardiovascular Risk Factors [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1870?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>White matter hyperintensities (WMHs) are frequently characterized as markers of cerebrovascular disease, whereas medial temporal atrophy (MTA) is a recognized marker of Alzheimer disease (AD). Our purpose was to test the reliability of a visual rating system (VRS) in evaluating WMHs and MTA and in distinguishing healthy from cognitively impaired subjects.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Subjects (<I>n</I> = 192) enrolled in the Florida Alzheimer's Disease Research Center were diagnosed with no cognitive impairment, nonamnestic mild cognitive impairment (na-MCI), amnestic MCI (a-MCI), or probable AD. The severity of WMHs was assessed on T2-weighted fluid-attenuated inversion recovery axial MR images, and the severity of MTA was evaluated on 1.5-mm-thick coronal MR images by using a computer-based visual rating system. Cardiovascular risk factor scores were calculated as the sum of 10 independent cardiovascular risk factors.</p>
</sec>
<sec><st>RESULTS:</st>
<p>WMH and MTA scores were greater in subjects with probable AD, relative to those with no cognitive impairment and na-MCI. MTA scores differentiated subjects with a-MCI from those with no cognitive impairment and na-MCI. The total WMH score was significantly related to MTA (<I>r</I> = 0.39; <I>P</I> &lt; .001) but not to cardiovascular risk factor scores (<I>r</I> = 0.07; <I>P</I> = not significant). The overall correct classification rate of probable AD versus no cognitive impairment by using MTA scores was 81.8%, improving to 86.5% when combined with WMH scores.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Both MTA and WMH scores distinguished subjects with no cognitive impairment and probable AD. Combining MTA and WMH scores improved the correct classification rate, whereas WMH scores were significantly related to MTA scores, but not to cardiovascular risk factor scores. This finding suggests that among subjects with a-MCI and probable AD, WMHs on MR images are primarily associated with neurodegenerative disease.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Appel, J., Potter, E., Bhatia, N., Shen, Q., Zhao, W., Greig, M.T., Raj, A., Barker, W.W., Potter, H., Schofield, E., Wu, Y., Loewenstein, D.A., Duara, R.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1693</dc:identifier>
<dc:title><![CDATA[Association of White Matter Hyperintensity Measurements on Brain MR Imaging with Cognitive Status, Medial Temporal Atrophy, and Cardiovascular Risk Factors [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1876</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1870</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1877?rss=1">
<title><![CDATA[CT Angiography Source Images Predict Final Infarct Extent in Patients with Basilar Artery Occlusion [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1877?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>The posterior circulation Acute Stroke Prognosis Early CT Score (pc-ASPECTS) is a 10-point grading system to quantify ischemic changes in the posterior circulation. We analyzed whether pc-ASPECTS on CT angiography (CTA) source images (CTASI) predicted the final infarct extent and hemorrhagic transformation (HT) rate in patients with basilar artery occlusion.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A pc-ASPECTS score of 10 indicates absence of visible ischemic changes in the posterior circulation, and pc-ASPECTS score of 0 indicates ischemic changes in the midbrain, pons, and bilateral thalami, posterior circulation territories, and cerebellar hemispheres. We retrospectively studied patients with basilar artery occlusion on CTA within 24 hours from symptom onset. We applied pc-ASPECTS to noncontrast CT (NCCT), CTASI, and follow-up images by 3-reader-consensus and assessed HT on follow-up images. We calculated Spearman correlation coefficients and performed linear regression analysis. Final infarct extent and HT rates were compared across dichotomized CTASI pc-ASPECTS groups (&ge; 8 vs &lt; 8).</p>
</sec>
<sec><st>RESULTS:</st>
<p>Among 43 patients, median (range) onset to CTA time was 5.0 hours (range, 0.7&ndash;24 hours). Pc-ASPECTS on CTASI (<I>r</I> = 0.75; <I>P</I> &lt; .001) but not NCCT (<I>r</I> = 0.29; <I>P</I> = .063) correlated with pc-ASPECTS on follow-up scans. Linear regression demonstrated a significant positive relationship between pc-ASPECTS on CTASI and follow-up scans (<I>R</I><sup>2</sup> = 0.58; <I>P</I> &lt; 01). Median follow-up pc-ASPECTS was lower in patients with a CTASI pc-ASPECTS &lt; 8 compared with patients with a CTASI pc-ASPECTS of 8 or more, respectively (<I>P</I> &lt; .001). HT rates were 27.3% vs 9.5%, respectively (<I>P</I> = .24). None of 8 patients without thrombolysis had HT on follow-up scans.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The extent of hypoattenuation on CTASI predicts the final infarct extent in patients with basilar artery occlusion.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Puetz, V., Sylaja, P.N., Hill, M.D., Coutts, S.B., Dzialowski, I., Becker, U., Gahn, G., von Kummer, R., Demchuk, A.M.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1723</dc:identifier>
<dc:title><![CDATA[CT Angiography Source Images Predict Final Infarct Extent in Patients with Basilar Artery Occlusion [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1883</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1877</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1884?rss=1">
<title><![CDATA[Imaging-Pathologic Correlation in Corticobasal Degeneration [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1884?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>The clinical diagnosis of corticobasal degeneration (CBD) is often difficult due to varied clinical manifestations. In 4 patients with neuropathologically confirmed CBD, characteristic imaging findings and correlations with neuropathologic features were evaluated. Furthermore, imaging findings in CBD were compared with neuropathologically confirmed progressive supranuclear palsy (PSP) for a differential diagnosis.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Four patients with neuropathologically confirmed CBD were studied. We evaluated the area of the tegmentum in the midsagittal plane, subcortical white matter (SCWM) abnormality, asymmetric cerebral atrophy, and signal-intensity abnormality in the subthalamic nuclei on MR imaging and compared them with histopathologic findings. Then, MR imaging findings in CBD were compared with those in 13 patients with PSP.</p>
</sec>
<sec><st>RESULTS:</st>
<p>On MR imaging, 3 patients had asymmetric cerebral atrophy extending to the central sulcus. On midsagittal sections, the mean midbrain tegmentum area was 66 mm<sup>2</sup>, being markedly smaller than normal, but there was no significant difference between PSP and CBD. All patients had signal-intensity abnormalities of the SCWM, constituting primary degeneration neuropathologically; however, no diffuse signal-intensity abnormality in the SCWM existed in the 13 patients with PSP. In 3 patients, T1-weighted images showed symmetric high signal intensity in the subthalamic nuclei. Neuropathologically, these areas showed characteristic CBD. MR imaging signal-intensity changes also existed in 4 patients with PSP; however, subthalamic nucleus degeneration was more severe in PSP than in CBD.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>In cases with midbrain tegmentum atrophy and signal-intensity changes in the subthalamic nuclei, the differential diagnosis distinguishing CBD from PSP based on MR imaging alone was difficult. White matter lesions and asymmetric atrophy can be useful for a differential diagnosis.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Tokumaru, A.M., Saito, Y., Murayama, S., Kazutomi, K., Sakiyama, Y., Toyoda, M., Yamakawa, M., Terada, H.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1721</dc:identifier>
<dc:title><![CDATA[Imaging-Pathologic Correlation in Corticobasal Degeneration [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1892</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1884</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1893?rss=1">
<title><![CDATA[Metachromatic Leukodystrophy: A Scoring System for Brain MR Imaging Observations [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1893?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Metachromatic leukodystrophy (MLD) is a devastating demyelinating disease for which novel therapies are being tested. We hypothesized that MR imaging of brain lesion involvement in MLD could be quantified along a scale.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Thirty-four brain MR images in 28 patients with proved biochemical and genetic defects for MLD were reviewed: 10 patients with late infantile, 16 patients with juvenile, and 2 patients with adult MLD. All MR images were reviewed by experienced neuroradiologists and neurologists (2 readers in Germany, 2 readers in the United States) for global disease burden, as seen on the T2 and fluid-attenuated inversion recovery images. A visual scoring method was based on a point system (range, 0&ndash;34) derived from the location of white matter involvement and the presence of global atrophy, analogous to the scoring system developed for adrenoleukodystrophy. The readers were blinded to the neurologic findings.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Thirty-three of 34 MR images showed confluent T2 hyperintensities of white matter. The inter-rater reliability coefficient was 0.988. Scores between readers were within 2 points of each other. Serial MR imaging studies in 6 patients showed significant progressive disease in 3 patients (initial score average, 4; mean follow-up, 24.3) and no change or 1 point progression in 3 patients (initial score average, 12; mean follow-up, 12.66). Projection fibers and the cerebellum tended to be involved only in advanced stages of disease.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The MLD MR severity scoring method can be used to provide a measure of brain MR imaging involvement in MLD patients.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Eichler, F., Grodd, W., Grant, E., Sessa, M., Biffi, A., Bley, A., Kohlschuetter, A., Loes, D.J., Kraegeloh-Mann, I.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1739</dc:identifier>
<dc:title><![CDATA[Metachromatic Leukodystrophy: A Scoring System for Brain MR Imaging Observations [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1897</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1893</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1898?rss=1">
<title><![CDATA[Is All "Communicating" Hydrocephalus Really Communicating? Prospective Study on the Value of 3D-Constructive Interference in Steady State Sequence at 3T [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1898?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>3D-constructive interference in steady state (3D-CISS) sequence has been used to assess the CSF pathways. The aim of this study was to investigate the additive value of 3D-CISS compared with conventional sequences in the diagnosis of obstructive membranes in hydrocephalus.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A total of 134 patients with hydrocephalus underwent MR imaging examination with a 3T unit consisting of turbo spin-echo, 3D-CISS, and cine phase-contrast (cine PC) sequences. 3D-CISS was used to assess obstructive membranes in CSF pathways compared with other sequences. Cine PC, follow-up imaging, and surgical findings were used to confirm obstructive membranes.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Comparing the number of noncommunicating cases by using the conventional and 3D-CISS images, we found 26 new cases (19.4%) of 134 cases that were previously misdiagnosed as communicating hydrocephalus by conventional images. 3D-CISS sequence identified obstructive membranes invisible in other sequences, which facilitated selection of neuroendoscopy in the treatment of 31 patients (23.1%) in total who would have been otherwise treated with shunt insertion. These patients included 26 newly diagnosed noncommunicating cases after demonstration of intraventricular and/or fourth ventricular outlet membranes and 5 cases of communicating hydrocephalus with obstructing cisternal membranes. There were obstructions of the foramina of Luschka in 22 of 26 newly found noncommunicating cases.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Conventional sequences are insensitive to obstructive membranes in CSF pathways, especially in the fourth ventricular exit foramina and the basal cisterns. 3D-CISS sequence, revealing these obstructive membranes, can alter patient treatment and prognosis.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Dincer, A., Kohan, S., Ozek, M.M.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1726</dc:identifier>
<dc:title><![CDATA[Is All "Communicating" Hydrocephalus Really Communicating? Prospective Study on the Value of 3D-Constructive Interference in Steady State Sequence at 3T [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1906</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1898</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1907?rss=1">
<title><![CDATA[Mild Hypoxic-Ischemic Injury in the Neonatal Rat Brain: Longitudinal Evaluation of White Matter Using Diffusion Tensor MR Imaging [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1907?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Selective white matter (WM) damage is a known sequela of mild hypoxic-ischemic (HI) injury in the neonatal rat model. The aim of this study was to evaluate longitudinally mild HI-induced WM damage (represented by the external capsule [EC]) by diffusion tensor MR imaging (DTI) and to correlate the findings with histology.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Seven-day-old Sprague-Dawley rats (<I>n</I> = <I>19</I>) underwent unilateral ligation of the left common carotid artery followed by hypoxia for 50 minutes to create mild HI injury. DTI was performed longitudinally at 5 time points from day 1 to day 90 postinjury (<I>n</I> = 19, 16, 13, 11, 9, respectively), and fractional anisotropy (FA), trace, radial diffusivity (<SUB></SUB>), and axial diffusivity (<SUB>//</SUB>) of the injury and control contralateral ECs were quantified. Rats were randomly sacrificed (<I>n</I> = 15, in total), and the corresponding ECs were stained with hematoxylin-eosin, Luxol fast blue (LFB), and neurofilament (NF) to evaluate morphologic changes, amount of myelin, and axonal count at every time point. A paired <I>t</I> test was applied to evaluate statistical differences between both ECs, and the Pearson correlation test was used to evaluate the relationships between DTI indices and histologic evaluations. In addition, longitudinal changes in DTI indices and histologic evaluations were analyzed by a linear mixed model and an analysis of variance test, respectively.</p>
</sec>
<sec><st>RESULTS:</st>
<p>We demonstrated significantly decreased FA, increased <SUB></SUB>, and similar <SUB>//</SUB> in the injury compared with the control EC, which was persistent through all time points. Histologic evaluation by LFB and NF staining showed reduced myelin stain intensity in the injury EC and similar axonal counts in both ECs. Longitudinally, there was an increase in FA, a decrease in <SUB></SUB> and trace, and stability in <SUB>//</SUB> in both ECs. Also, there was progressive reduction in the differences in FA, trace, and <SUB></SUB> between the injury and control EC, especially between day 1 and day 7 postinjury and in tandem with changes in myelin stain. FA was significantly correlated with myelin stain (<I>r</I> = 0.681, <I>P</I> &lt; .01) and axonal count (<I>r</I> = 0.673, <I>P</I> &lt; .01), whereas <SUB></SUB> was significantly correlated with myelin stain only (<I>r</I> = &ndash;0.528, <I>P</I> &lt; .01), and <SUB>//</SUB>, with axonal count only (<I>r</I> = 0.372, <I>P</I> = .043).</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Diffusion indices can reflect dysmyelination in mild HI injury, continual myelination of both injury and control ECs with growth, and the partial recovery of myelin postinjury. We propose that diffusion indices may be used as biomarkers to monitor noninvasively the longitudinal changes of mild HI-induced WM damage.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wang, S., Wu, E.X., Cai, K., Lau, H.-F., Cheung, P.-T., Khong, P.-L.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1697</dc:identifier>
<dc:title><![CDATA[Mild Hypoxic-Ischemic Injury in the Neonatal Rat Brain: Longitudinal Evaluation of White Matter Using Diffusion Tensor MR Imaging [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1913</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1907</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1914?rss=1">
<title><![CDATA[Automated Optimization of Subcortical Cerebral MR Imaging-Atlas Coregistration for Improved Postoperative Electrode Localization in Deep Brain Stimulation [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1914?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>The efficacy of deep brain stimulation in treating movement disorders depends critically on electrode localization, which is conventionally described by using coordinates relative to the midcommissural point. This approach requires manual measurement and lacks spatial normalization of anatomic variances. Normalization is based on intersubject spatial alignment (coregistration) of corresponding brain structures by using different geometric transformations. Here, we have devised and evaluated a scheme for automated subcortical optimization of coregistration (ASOC), which maximizes patient-to-atlas normalization accuracy of postoperative structural MR imaging into the standard Montreal Neurologic Institute (MNI) space for the basal ganglia.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Postoperative T2-weighted MR imaging data from 39 patients with Parkinson disease and 32 patients with dystonia were globally normalized, representing the standard registration (control). The global transformations were regionally refined by 2 successive linear registration stages (RSs) (ASOC-1 and 2), focusing progressively on the basal ganglia with 2 anatomically selective brain masks, which specify the reference volume (weighted cost function). Accuracy of the RSs was quantified by spatial dispersion of 16 anatomic landmarks and their root-mean-square errors (RMSEs) with respect to predefined MNI-based reference points. The effects of CSF volume, age, and sex on RMSEs were calculated.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Mean RMSEs differed significantly (<I>P</I> &lt; .001) between the global control (4.2 &plusmn; 2.0 mm), ASOC-1 (1.92 &plusmn; 1.02 mm), and ASOC-2 (1.29 &plusmn; 0.78 mm).</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The present method improves the registration accuracy of postoperative structural MR imaging data into MNI space within the basal ganglia, allowing automated normalization with increased precision at stereotactic targets, and enables lead-contact localization in MNI coordinates for quantitative group analysis.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Schonecker, T., Kupsch, A., Kuhn, A.A., Schneider, G.-H., Hoffmann, K.-T.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1741</dc:identifier>
<dc:title><![CDATA[Automated Optimization of Subcortical Cerebral MR Imaging-Atlas Coregistration for Improved Postoperative Electrode Localization in Deep Brain Stimulation [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1921</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1914</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1922?rss=1">
<title><![CDATA[Smaller Gray Matter Volumes in Frontal and Parietal Cortices of Solvent Abusers Correlate with Cognitive Deficits [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1922?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Abuse of toluene-containing organic solvents by inhalation is a prevalent practice among adolescents. Long-term abuse of toluene causes cognitive deficits. The mechanism of cognitive deficits induced by long-term toluene abuse has not yet been defined. In the current study, we assessed the effects of chronic toluene abuse on cortical gray matter volume and the association between cognitive impairment and cortical gray matter volume distribution in chronic toluene abusers.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Fifteen toluene abusers and 20 healthy control subjects matched in sex, age, education level, and handedness were investigated by structural MR imaging. The cognitive states of the subjects were assessed by using the third edition of the <I>Wechsler Intelligence Scale for Children</I> (WISC-III). The voxel-based comparison and correlation analyses of MR images were performed by using SPM5 software.</p>
</sec>
<sec><st>RESULTS:</st>
<p>The voxel-based morphometric analysis revealed that toluene abusers had significantly lower gray matter volumes in the bilateral frontotemporal and right parietal cortices. In addition, the lower gray matter volumes in the frontal and parietal regions correlated with the duration of toluene abuse. There was a positive correlation between the WISC performance scale scores and gray matter volumes in the frontal and parietal cortices of the abusers.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The results of the current study demonstrate that chronic toluene abusers have smaller gray matter volumes than nonabusers in various regions of the brain. Moreover, the cognitive deficits are associated with the lower gray matter volumes in the frontal and parietal cortices of chronic toluene abusers.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Aydin, K., Kircan, S., Sarwar, S., Okur, O., Balaban, E.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1728</dc:identifier>
<dc:title><![CDATA[Smaller Gray Matter Volumes in Frontal and Parietal Cortices of Solvent Abusers Correlate with Cognitive Deficits [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1928</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1922</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1929?rss=1">
<title><![CDATA[An Automatic Procedure for Normalization of Cerebral Blood Volume Maps in Dynamic Susceptibility Contrast-Based Glioma Imaging [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1929?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>To characterize gliomas from dynamic susceptibility contrast (DSC)&ndash;based cerebral blood volume (CBV) maps, a CBV value from a normal-appearing region of interest is typically identified manually and used to normalize the CBV maps. This method is user-dependent and time-consuming. We propose an alternative approach based on automatic identification of normal-appearing first-pass curves from brain tissue. Our results in 101 patients suggest similar or better diagnostic accuracy values than the manual approach.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Emblem, K.E., Bjornerud, A.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1680</dc:identifier>
<dc:title><![CDATA[An Automatic Procedure for Normalization of Cerebral Blood Volume Maps in Dynamic Susceptibility Contrast-Based Glioma Imaging [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1932</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1929</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1933?rss=1">
<title><![CDATA[Focal Neuronal Gigantism: A Rare Complication of Therapeutic Radiation [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1933?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Radiation therapy, a mainstay in the treatment of many brain tumors, results in a variety of well-documented acute and chronic complications. Isolated cortical damage following irradiation represents an extremely rare delayed therapeutic complication, described only twice in the medical literature. We report this rare delayed complication in a patient following treatment of a right frontal anaplastic oligodendroglioma.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Gaughen, J.R., Bourne, T.D., Aregawi, D., Shah, L.M., Schiff, D.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1671</dc:identifier>
<dc:title><![CDATA[Focal Neuronal Gigantism: A Rare Complication of Therapeutic Radiation [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1935</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1933</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1936?rss=1">
<title><![CDATA[The Value of Routine Clinical and Radiologic Studies in Predicting Neoplastic Invasion of Cricoarytenoid Units [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1936?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Evaluation of the laryngeal cartilages is essential for the treatment strategy of patients with laryngeal carcinoma. Our aim was to assess the accuracy of preoperative clinical examinations and CT for preoperative evaluation.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A prospective comparative study was performed at a university department on 30 patients with advanced laryngeal carcinomas. All patients were men and underwent total laryngectomy. The preoperative mobility of vocal folds was evaluated and classified as mobile, impaired, or fixed. CT was performed by using multidetector row CT. Cricoarytenoid units (CAUs) from the laryngectomy specimens were cut into sections. Histologic findings were compared with the clinical and radiologic findings.</p>
</sec>
<sec><st>RESULTS:</st>
<p>The accuracy of combined clinical and CT staging in CAUs with normal mobility, impaired mobility, and absent mobility and negative CT findings was 96.5%, 50%, and 80%, respectively. These scores were 40%, 54.5%, and 83.3% for CAUs with normal mobility, impaired mobility, and absent mobility and positive CT findings, respectively.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Arytenoid mobility and &gt;1 cartilage abnormality on CT were found to be reliable indicators of neoplastic cartilage invasion in patients with laryngeal carcinoma.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Cagli, S., Ozturk, M., Yuce, I., Deniz, K., Guney, E.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1692</dc:identifier>
<dc:title><![CDATA[The Value of Routine Clinical and Radiologic Studies in Predicting Neoplastic Invasion of Cricoarytenoid Units [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1940</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1936</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1941?rss=1">
<title><![CDATA[Inflammatory Pseudotumor of the Trigeminal Nerve: A Neoplastic Mimic You Do Not Want to Miss [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1941?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Inflammatory pseudotumor is a rare non-neoplastic mass that may clinically and radiologically mimic a spectrum of benign and malignant neoplasms. It is uncommon in the head and neck and particularly rare at the skull base. We present a case of pseudotumor originating from the trigeminal nerve in a patient who presented with headache and facial numbness. A high index of suspicion is necessary to diagnose this benign but locally aggressive entity.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Seol, J.G., Loevner, L.A., O'Malley, B.W., Grady, M.S.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:23 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1641</dc:identifier>
<dc:title><![CDATA[Inflammatory Pseudotumor of the Trigeminal Nerve: A Neoplastic Mimic You Do Not Want to Miss [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1943</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1941</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1944?rss=1">
<title><![CDATA[Unilateral Hypopharyngitis, Cellulitis, and a Multinodular Goiter: A Triad of Findings Suggestive of Acute Suppurative Thyroiditis [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1944?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Acute suppurative thyroiditis is an uncommon disorder, which has been associated with pre-existing thyroid disease, especially a multinodular goiter. We describe a case of a woman who presented clinically with an acute inflammatory condition of the neck. On CT examination, she had a triad of a multinodular goiter, a unilateral hypopharyngitis, and a surrounding cellulitis. We suggest that the constellation of these imaging findings should alert the radiologist to the diagnosis of acute thyroiditis.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Dugar, M., da Graca Bandeira, A., Bruns, J., Som, P.M.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1642</dc:identifier>
<dc:title><![CDATA[Unilateral Hypopharyngitis, Cellulitis, and a Multinodular Goiter: A Triad of Findings Suggestive of Acute Suppurative Thyroiditis [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1946</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1944</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1947?rss=1">
<title><![CDATA[Voxel-Based Analysis of T2 Hyperintensities in White Matter during Treatment of Childhood Leukemia [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1947?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>White matter (WM) hyperintensities on T2-weighted MR imaging are the most common imaging manifestation of neurotoxic effects of therapy for central nervous system (CNS) prophylaxis in childhood acute lymphoblastic leukemia (ALL). This study uses voxel-based analyses (VBA) of T2-weighted imaging of patients during treatment to identify which WM regions are preferentially damaged.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Two sets of conventional T2-weighted axial images were acquired on a 1.5T MR imaging scanner from 197 consecutive patients (85 female, 112 male; aged 1.0&ndash;18.9 years) enrolled on an institutional ALL treatment protocol. Images were acquired after completion of induction therapy and after the final of the 4 courses of intravenous high-dose methotrexate in consolidation therapy (3.9 &plusmn; 0.8 months apart). Voxel-wise statistical testing of the incremental change between normalized longitudinal T2 images was performed with radiologist reading (normal or abnormal) and treatment risk-group as covariates.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Two highly significant bilateral clusters of T2 signal intensity change were identified in both 1-group and 2-group analyses. The regions were symmetric in size, shape, and average signal intensity. Increased T2-weighted signal intensity from these regions both within and between examinations were nonlinear functions of age at examination, and the difference between the examinations was greater for older subjects who received more intense therapy.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>These analyses identified specific WM tracts involving predominantly the anterior, superior, and posterior corona radiata and superior longitudinal fasciculus, which were at increased risk for the development of T2-weighted hyperintensities during therapy for childhood ALL. These vulnerable regions may be the cause of subsequent cognitive difficulties consistently observed in survivors.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Reddick, W.E., Glass, J.O., Johnson, D.P., Laningham, F.H., Pui, C.-H.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1733</dc:identifier>
<dc:title><![CDATA[Voxel-Based Analysis of T2 Hyperintensities in White Matter during Treatment of Childhood Leukemia [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1954</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1947</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1955?rss=1">
<title><![CDATA[The Anatomic Variations of the Circle of Willis in Preterm-at-Term and Term-Born Infants: An MR Angiography Study at 3T [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1955?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>It has been shown that the brain of a preterm infant develops differently from that of a term infant, but little is known about the neonatal cerebrovascular anatomy. Our aims were to establish reference data for the prevalence of the anatomic variations of the neonatal circle of Willis (CoW) and to explore the effect of prematurity, MR imaging abnormality, vascular-related abnormality, laterality, and sex on these findings.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>We scanned 103 infants with an optimized MR angiography (MRA) protocol. Images were analyzed for different variations of the CoW, and results were compared for the following: 1) preterm-at-term and term-born infants, 2) infants with normal and abnormal MR imaging, 3) infants with and without a vascular-related abnormality, 4) boys and girls, and 5) left- and right-sided occurrence.</p>
</sec>
<sec><st>RESULTS:</st>
<p>The most common anatomic variation was absence/hypoplasia of the posterior communicating artery. Preterm infants at term had a higher prevalence of a complete CoW and a lower prevalence of anatomic variations compared with term-born infants; this finding was significant for the anterior cerebral artery (<I>P</I> = .02). There was increased prevalence of variations of the major cerebral arteries in those infants with vascular-related abnormalities, statistically significant for the posterior cerebral artery (<I>P</I> = .004). There was no statistically significant difference between boys and girls and left/right variations.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Prematurity is associated with more complete CoWs and fewer anatomic variations. In vascular-related abnormalities, more variations involved major arterial segments, but fewer variations occurred in the communicating arteries. Overall reference values of the variations match those of the general adult population.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Malamateniou, C., Adams, M.E., Srinivasan, L., Allsop, J.M., Counsell, S.J., Cowan, F.M., Hajnal, J.V., Rutherford, M.A.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1724</dc:identifier>
<dc:title><![CDATA[The Anatomic Variations of the Circle of Willis in Preterm-at-Term and Term-Born Infants: An MR Angiography Study at 3T [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1962</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1955</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1963?rss=1">
<title><![CDATA[Diffusion Tensor Imaging Study of the Cortical Origin and Course of the Corticospinal Tract in Healthy Children [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1963?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Several studies have questioned the traditional belief that the corticospinal tract (CST) arises exclusively from the precentral gyrus and passes through the anterior half of the posterior limb of the internal capsule (PLIC) in humans; however, no direct evidence existed from structural imaging, and developmental aspects of CST origin have not been clarified. We used diffusion tensor imaging (DTI) tractography to test the hypotheses that CST can originate from both pre- and postcentral gyri and is located posteriorly in the PLIC, and we also determined how age, sex, or handedness affected these locations.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Forty-two healthy children (2.6&ndash;17.5 years of age; 20 girls) underwent DTI. Subsequently, tractography was performed on the basis of fiber assignment by continuous tracking (FACT) algorithm and brute force approach, with a fractional anisotropy (FA) threshold of &lt;0.2 and an angle threshold of &gt;50&deg;. The CST was isolated by using a knowledge-based region-of-interest approach, and its cortical origin and location on the PLIC was determined.</p>
</sec>
<sec><st>RESULTS:</st>
<p>DTI revealed that the CST originated from both pre- and postcentral gyri in 71.4% of hemispheres, from the precentral gyrus only in 19%, and from the postcentral gyrus only in 7.1%. The overall distribution was similar in both hemispheres. However, children with CST originating from both pre- and postcentral gyri were older (mean, 11.1 years of age) than those with precentral origin (mean, 5.8 years of age) or postcentral origin (mean, 7.8 years of age) only (<I>P</I> = .00003). The center of the CST was localized at 65% of the length (from its anterior margin) of the PLIC, and the CST occupied 26.5% of its anteroposterior length. There was a significant positive correlation between age and FA of the CST (<I>r</I> = 0.49; <I>P</I> = .002). The volume of the precentral portion of the left CST was significantly higher than that of its postcentral portion (<I>P</I> = .01) and that of the right CST (<I>P</I> = .0002). The pattern of cortical origin of CST, its location at the level of PLIC, and its volume and FA were unaffected by sex or handedness.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The CST most frequently originates from both pre- and postcentral gyri, especially in older children, and is typically centered approximately two thirds of the distance from the anterior margin of the PLIC and occupies about a quarter of its anteroposterior length. In young children, the CST can often be seen originating exclusively from the precentral gyrus by DTI.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kumar, A., Juhasz, C., Asano, E., Sundaram, S.K., Makki, M.I., Chugani, D.C., Chugani, H.T.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1742</dc:identifier>
<dc:title><![CDATA[Diffusion Tensor Imaging Study of the Cortical Origin and Course of the Corticospinal Tract in Healthy Children [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1970</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1963</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1971?rss=1">
<title><![CDATA[Aicardi-Goutieres Syndrome: Neuroradiologic Findings and Follow-Up [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1971?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>To date, few studies have focused specifically on imaging findings in Aicardi-Gouti&egrave;res syndrome (AGS). We set out to evaluate retrospectively neuroradiologic data from a large sample of patients with AGS, focusing on the pattern of white matter abnormalities and the temporal evolution of the cerebral involvement to establish the radiologic natural history of the disease.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Thirty-six patients, 18 girls and 18 boys, were included. All had a clinical diagnosis of AGS, genetically confirmed in 31 of them. For every subject, we reviewed at least 1 CT and 1 MR imaging study; 19 (52.7%) had multiple examinations. In all, we reviewed 109 examinations. Clinical-neuroradiologic comparisons were analyzed by using the <sup>2</sup> test.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Calcifications were found in all subjects, mainly in the basal ganglia, lobar white matter, and dentate nuclei. Abnormal white matter was present in all the subjects, showing 2 patterns of distribution: diffuse in 18 (50%) and an anteroposterior gradient in 18 (50%). Cystic areas were observed in the temporal and/or frontal lobes in 12/36 patients (33.3%). A correlation was found between early age at onset and severity of the leukoencephalopathy in the frontal (<I>P</I> = .024) and temporal (<I>P</I> = .034) regions. A significant degree of cerebral atrophy was found in 31/36 subjects (86.1%). The neuroradiologic presentation remained substantially stable with time.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The different neuroradiologic presentations of AGS are here outlined for the first time in a large sample of patients. These findings may facilitate more precise and earlier diagnosis of this rare but probably underdiagnosed syndrome.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Uggetti, C., La Piana, R., Orcesi, S., Egitto, M.G., Crow, Y.J., Fazzi, E.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1694</dc:identifier>
<dc:title><![CDATA[Aicardi-Goutieres Syndrome: Neuroradiologic Findings and Follow-Up [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1976</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1971</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1977?rss=1">
<title><![CDATA[Improvement of Clinical Language Localization with an Overt Semantic and Syntactic Language Functional MR Imaging Paradigm [FUNCTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1977?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Functional MR imaging (fMRI) is a promising but, in some aspects, still debated noninvasive tool for functional language mapping. We developed a clinical fMRI overt language design at the sentential level to optimize sensitivity for language-related areas of the brain. To evaluate applicability and sensitivity, we investigated a consecutive series of presurgical patients with epilepsy with minimal morphologic brain abnormalities.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Thirty right-handed patients with temporal lobe epilepsy (TLE) and a control group of 23 right-handed healthy subjects participated in the study. The language design included semantic and syntactic error-detection tasks and was constructed to represent the most relevant aspects of everyday language demands. It was applied during block-designed fMRI runs. We performed image preprocessing and statistical analysis with SPM5 at a group level, applying widely used statistical criteria. The study was approved by the local ethics committee, and all participants gave written informed consent.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Given the strict statistical criteria, the sensitivity for inferior frontal and posterior temporal activations (comprising Broca and Wernicke regions) was improved relative to previous findings in the literature. For both language areas, we found 100% sensitivity in healthy subjects (Brodmann areas, BA22 and BA44) and 97% sensitivity in patients (when including BA47). Lateralization results demonstrated the capability to detect atypical language lateralizations in patients, which were more frequent in than those in healthy subjects.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>We developed a clinical language fMRI design that integrates various relevant aspects of everyday language demands and provides robust localization of core language areas.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Gartus, A., Foki, T., Geissler, A., Beisteiner, R.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1725</dc:identifier>
<dc:title><![CDATA[Improvement of Clinical Language Localization with an Overt Semantic and Syntactic Language Functional MR Imaging Paradigm [FUNCTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1985</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1977</prism:startingPage>
<prism:section>FUNCTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1986?rss=1">
<title><![CDATA[Long-Term Follow-Up of 1036 Cerebral Aneurysms Treated by Bare Coils: A Multicentric Cohort Treated between 1998 and 2003 [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1986?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>The endovascular treatment (EVT) of cerebral aneurysms has experienced a revolution since 1991 with the introduction of platinum coil technology. During the past 10 years, there has been significant study of the feasibility of this technique, and clinical results of EVT have been published. The long-term durability of Guglielmi detachable coil (GDC) embolization of cerebral aneurysms still remains unknown. The purpose of this study was to evaluate the stability of anatomic occlusion of aneurysms and to assess the rate of recanalization and retreatment of these aneurysms.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Between January 1998 and December 2003, 1036 aneurysms (804 ruptured and 232 nonruptured) were treated consecutively with GDC coils in 5 neuroradiology centers. Procedural feasibility, acute angiographic occlusion results, morbidity, and mortality associated with this technique were assessed. All patients were regularly followed by digital subtraction angiography and MR imaging each year after treatment.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Initial acute angiographic results in 1036 aneurysms demonstrated total occlusion in 731 patients (70.5%), subtotal occlusion in 252 (24.3%), incomplete occlusion in 20 (1.9%), and failures in 33% (3.3%) aneurysms. A remodeling technique was used in 10%. A second procedure was performed for 72 aneurysms (7%). The total aneurysm follow-up time was 49,923 months (4160.25 aneurysm-years). The retreatment period was either in the months following initial treatment in aneurysms incompletely occluded or in years due to recanalization or de novo aneurysms. Fewer than 5 patients rebled during 10 years of follow-up. Long-term follow-up angiograms were obtained in 899 aneurysms, with 646 total, 230 subtotal, and 23 incomplete results.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Long-term follow-up of cerebral aneurysms is necessary to depict recanalization. Only 7% of the aneurysms were retreated. Use of bare coils gives a good long-term level of occlusion.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Gallas, S., Januel, A.C., Pasco, A., Drouineau, J., Gabrillargues, J., Gaston, A., Cognard, C., Herbreteau, D.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1744</dc:identifier>
<dc:title><![CDATA[Long-Term Follow-Up of 1036 Cerebral Aneurysms Treated by Bare Coils: A Multicentric Cohort Treated between 1998 and 2003 [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1992</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1986</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1993?rss=1">
<title><![CDATA[Carotid Artery Stents: In Vitro Comparison of Different Stent Designs and Sizes Using CT Angiography and Contrast-Enhanced MR Angiography at 1.5T and 3T [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1993?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>CT angiography (CTA) and MR angiography (MRA) are increasingly used methods for evaluation of stented vessel segments. Our aim was to compare CTA, contrast-enhanced MRA (CE-MRA) at 1.5T, and CE-MRA at 3T for the visualization of carotid artery stents and to define the best noninvasive imaging technique as an alternative to conventional angiography for each stent.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>CTA and CE-MRA appearances of 18 carotid artery stents of different designs and sizes (4.0 to 10.0 mm) were investigated in vitro. For each stent, artificial lumen narrowing (ALN) was calculated.</p>
</sec>
<sec><st>RESULTS:</st>
<p>With CE-MRA at 3T and at 1.5T, ALN in most nitinol stents was lower than that in the groups of stainless steel and cobalt alloy stents. In most nitinol stents and in both cobalt alloy stents, ALN was lower on CE-MRA at 3T than at 1.5T. In all stainless steel stents, ALN was lower on CTA than on CE-MRA. With CTA and CE-MRA, in most stents ALN decreased with increasing stent diameter.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>CTA and CE-MRA evaluation of vessel patency after stent placement is possible but is considerably impaired by ALN. Investigators should be informed about the method of choice for every stent. Stent manufacturers should be aware of potential artifacts caused by their stents during noninvasive diagnostic methods such as CTA and CE-MRA.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lettau, M., Sauer, A., Heiland, S., Rohde, S., Bendszus, M., Hahnel, S.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1743</dc:identifier>
<dc:title><![CDATA[Carotid Artery Stents: In Vitro Comparison of Different Stent Designs and Sizes Using CT Angiography and Contrast-Enhanced MR Angiography at 1.5T and 3T [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1997</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1993</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/10/1998?rss=1">
<title><![CDATA[Symptomatic Perianeurysmal Edema Following Bare Platinum Embolization of a Small Unruptured Cerebral Aneurysm [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/10/1998?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>There is considerable interest in the development of symptomatic inflammatory reactions following coil embolization of cerebral aneurysms. Patients have experienced a range of adverse events, usually after treatment of moderately large aneurysms with modified "bioactive" coils. More recently, it has been recognized that adverse inflammatory reactions can be associated with the use of "nonbioactive" coils, and we present a case of symptomatic perianeurysmal edema after treatment of a small unruptured aneurysm with bare platinum coils.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Craven, I., Patel, U.J., Gibson, A., Coley, S.C.]]></dc:creator>
<dc:date>Fri, 13 Nov 2009 10:02:24 PST</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1643</dc:identifier>
<dc:title><![CDATA[Symptomatic Perianeurysmal Edema Following Bare Platinum Embolization of a Small Unruptured Cerebral Aneurysm [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>2000</prism:endingPage>
<prism:publicationDate>2009-11-01</prism:publicationDate>
<prism:startingPage>1998</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E128?rss=1">
<title><![CDATA[Brain Diffusion-Weighted and Diffusion Tensor Imaging Findings in an Infant with Biotinidase Deficiency [LETTERS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E128?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Soares-Fernandes, J.P., Magalhaes, Z., Rocha, J.F., Barkovich, A.J.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1703</dc:identifier>
<dc:title><![CDATA[Brain Diffusion-Weighted and Diffusion Tensor Imaging Findings in an Infant with Biotinidase Deficiency [LETTERS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E128</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E128</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E129?rss=1">
<title><![CDATA[Practicing Lateral Cervical Puncture for Myelography [LETTERS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E129?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Mironov, A.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1683</dc:identifier>
<dc:title><![CDATA[Practicing Lateral Cervical Puncture for Myelography [LETTERS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E129</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E129</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E130?rss=1">
<title><![CDATA[Klippel-Feil Syndrome and Anterior Cervical Meningomyelocele: A Rare Case Report [LETTERS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E130?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Balachandran, G.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1730</dc:identifier>
<dc:title><![CDATA[Klippel-Feil Syndrome and Anterior Cervical Meningomyelocele: A Rare Case Report [LETTERS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E130</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E130</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E131?rss=1">
<title><![CDATA[Intraprocedural Rupture of Aneurysms: Not Necessarily a Small Problem [LETTERS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E131?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Elijovich, L., Johnston, S.C.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1759</dc:identifier>
<dc:title><![CDATA[Intraprocedural Rupture of Aneurysms: Not Necessarily a Small Problem [LETTERS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E131</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E131</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E132?rss=1">
<title><![CDATA[Reply: [LETTERS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E132?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[van Rooij, W.J., Sluzewski, M.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1772</dc:identifier>
<dc:title><![CDATA[Reply: [LETTERS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E132</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E132</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E133?rss=1">
<title><![CDATA[Operative Techniques in Epilepsy Surgery [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E133?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Baltuch, G.H., Villemure, J.-G.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1689</dc:identifier>
<dc:title><![CDATA[Operative Techniques in Epilepsy Surgery [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E133</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E133</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E134?rss=1">
<title><![CDATA[Motion Preservation Surgery of the Spine: Advanced Techniques and Controversies [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E134?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Yue, J.J., Bertagnoli, R., McAfee, P.C., An, H.S.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1707</dc:identifier>
<dc:title><![CDATA[Motion Preservation Surgery of the Spine: Advanced Techniques and Controversies [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E134</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E134</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E135?rss=1">
<title><![CDATA[Handbook of Cerebrovascular Disease and Neurointerventional Technique [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E135?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Harrigan, M.R., Deveikis, J.P.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1708</dc:identifier>
<dc:title><![CDATA[Handbook of Cerebrovascular Disease and Neurointerventional Technique [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E135</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E135</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E136?rss=1">
<title><![CDATA[Diagnostic Neuroradiology [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E136?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Kornienko, V.N., Pronin, I.N.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1709</dc:identifier>
<dc:title><![CDATA[Diagnostic Neuroradiology [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E136</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E136</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E137?rss=1">
<title><![CDATA[Tumors of the Spine [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E137?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Kim, D.H., Chang, U.-K., Kim, S.-H., Bilsky, M.H.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1719</dc:identifier>
<dc:title><![CDATA[Tumors of the Spine [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E137</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E137</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E138?rss=1">
<title><![CDATA[Osteoporosis: Two-Volume Set, 3rd ed. [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E138?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Marcus, R., Feldman, D., Nelson, D.A, Rosen, C.J.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1711</dc:identifier>
<dc:title><![CDATA[Osteoporosis: Two-Volume Set, 3rd ed. [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E138</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E138</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E139?rss=1">
<title><![CDATA[Principles of Bone Biology, 3rd ed. [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E139?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Bilezikan, J.P., Raisz, L.G., Martin, T.J.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1712</dc:identifier>
<dc:title><![CDATA[Principles of Bone Biology, 3rd ed. [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E139</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E139</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E140?rss=1">
<title><![CDATA[Atlas of Spine Trauma: Adult and Pediatric [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E140?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Kim, D.H., Ludwig, S.C., Vaccaro, A.R., Chang, J.-C.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1713</dc:identifier>
<dc:title><![CDATA[Atlas of Spine Trauma: Adult and Pediatric [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E140</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E140</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E141?rss=1">
<title><![CDATA[Normal Findings in Radiography [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E141?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Moeller, T.B.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1717</dc:identifier>
<dc:title><![CDATA[Normal Findings in Radiography [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E141</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E141</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E142?rss=1">
<title><![CDATA[PET and PET/CT: A Clinical Guide, 2nd ed. [BOOK REVIEWS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E142?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Lin, E.C., Alavi, A.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1720</dc:identifier>
<dc:title><![CDATA[PET and PET/CT: A Clinical Guide, 2nd ed. [BOOK REVIEWS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E142</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E142</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E143?rss=1">
<title><![CDATA[BOOKS RECEIVED [BOOKS RECEIVED]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E143?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:title><![CDATA[BOOKS RECEIVED [BOOKS RECEIVED]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E143</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E143</prism:startingPage>
<prism:section>BOOKS RECEIVED</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/E144?rss=1">
<title><![CDATA[Erratum [ERRATA]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/E144?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:16 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1878</dc:identifier>
<dc:title><![CDATA[Erratum [ERRATA]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>E144</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>E144</prism:startingPage>
<prism:section>ERRATA</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1627?rss=1">
<title><![CDATA[Preservation of Knowledge, Part 1: Paper and Microfilm [PERSPECTIVES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1627?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Castillo, M.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1655</dc:identifier>
<dc:title><![CDATA[Preservation of Knowledge, Part 1: Paper and Microfilm [PERSPECTIVES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1628</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1627</prism:startingPage>
<prism:section>PERSPECTIVES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1628?rss=1">
<title><![CDATA[Second Branchial Cleft Cyst: NOT!! [EDITORIALS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1628?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Hudgins, P.A., Gillison, M.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1729</dc:identifier>
<dc:title><![CDATA[Second Branchial Cleft Cyst: NOT!! [EDITORIALS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1629</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1628</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1630?rss=1">
<title><![CDATA[Review of Portable CT with Assessment of a Dedicated Head CT Scanner [REVIEW ARTICLES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1630?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>This article reviews a number of portable CT scanners for clinical imaging. These include the CereTom, Tomoscan, xCAT ENT, and OTOscan. The Tomoscan scanner consists of a gantry with multisection detectors and a detachable table. It can perform a full-body scanning, or the gantry can be used without the table to scan the head. The xCAT ENT is a conebeam CT scanner that is intended for intraoperative scanning of cranial bones and sinuses. The OTOscan is a multisection CT scanner intended for imaging in ear, nose, and throat settings and can be used to assess bone and soft tissue of the head. We also specifically evaluated the technical and clinical performance of the CereTom, a scanner designed specifically for neuroradiologic head imaging. The contrast performance of this scanner permitted the detection of 4-mm low-contrast lesions, and the limiting spatial resolution was 7 line pairs per centimeter. The measured volume of the CT dose index (CTDI<SUB>vol</SUB>) for a standard head CT scan was 41 mGy (120 kV/14 mAs). All clinical images were of diagnostic quality, and the average patient effective dose was 1.7 mSv. We conclude that the CereTom portable CT scanner generates satisfactory clinical images at acceptable patient doses.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Rumboldt, Z., Huda, W., All, J.W.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1603</dc:identifier>
<dc:title><![CDATA[Review of Portable CT with Assessment of a Dedicated Head CT Scanner [REVIEW ARTICLES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1636</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1630</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1637?rss=1">
<title><![CDATA[Endovascular Treatment of Epistaxis [REVIEW ARTICLES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1637?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Epistaxis is a common condition that can be managed conservatively in most cases. When these measures, including anterior and posterior packing of the nasal cavity, are unsuccessful at controlling the bleeding, interruption of the blood supply to the sinonasal area can be performed, either by surgical ligation or by transarterial embolization. Embolization should be preceded by thorough diagnostic angiography. Aside from aiding with subsequent selective catheterization and embolization, such angiography may reveal significant anatomic anomalies, anastomoses, or an unsuspected cause of epistaxis. Taking these findings into account, the interventionalist may decide to refrain from embolization or adjust the technique to minimize the risk of adverse events, which are mostly related to inadvertent embolization of the internal carotid artery or ophthalmic artery. We present a review of the various causes of epistaxis and the treatment options, with emphasis on endovascular embolization. We also describe the protocol of our institution for endovascular management of this condition.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Willems, P.W.A., Farb, R.I., Agid, R.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1607</dc:identifier>
<dc:title><![CDATA[Endovascular Treatment of Epistaxis [REVIEW ARTICLES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1645</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1637</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1646?rss=1">
<title><![CDATA[Opinion: Imaging Follow-Up after Coiling of Intracranial Aneurysms [RESEARCH PERSPECTIVES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1646?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Coiling is increasingly used as treatment for intracranial aneurysms with favorable short-term outcome. Concern exists about long-term reopening and the inherent risk of recurrent subarachnoid hemorrhage (SAH), and long-term imaging follow-up is advocated. It is unknown for how long and how often coiled aneurysms need to be followed and what subgroups carry a higher or lower risk for reopening. Recently, new data have become available that concern the designation of an optimal long-term follow-up protocol. Three studies focused on a special subgroup, the coiled aneurysms that are adequately occluded at 6 months. This subgroup comprises about 80% of all coiled aneurysms. In these aneurysms, the risk of reopening that needs retreatment during the next 5&ndash;10 years is very low. In addition, the risk of recurrent SAH is almost zero, even lower than that after clipping. Within the first 5 years after coiling, the incidence of the development of de novo aneurysms or enlargement of existing untreated aneurysms is low, with an extremely low risk of recurrent SAH from these aneurysms. These data suggest that aneurysms that are adequately occluded at 6 months after coiling, in general, do not need prolonged imaging follow-up in the next 5&ndash;10 years. More data are needed to identify possible subgroups with adequately occluded coiled aneurysms at 6 months that behave differently on longer follow-up, such as giant aneurysms, partially thrombosed aneurysms, or patients with a positive family history.</p>
</sec>
]]></description>
<dc:creator><![CDATA[van Rooij, W.J., Sluzewski, M.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1673</dc:identifier>
<dc:title><![CDATA[Opinion: Imaging Follow-Up after Coiling of Intracranial Aneurysms [RESEARCH PERSPECTIVES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1648</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1646</prism:startingPage>
<prism:section>RESEARCH PERSPECTIVES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1649?rss=1">
<title><![CDATA[Counterpoint: Has the Last Word Been Said? [COMMENTARIES]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1649?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Raymond, J.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1690</dc:identifier>
<dc:title><![CDATA[Counterpoint: Has the Last Word Been Said? [COMMENTARIES]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1652</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1649</prism:startingPage>
<prism:section>COMMENTARIES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1653?rss=1">
<title><![CDATA[Treatment of Stenoses of Vertebral Artery Origin Using Short Drug-Eluting Coronary Stents: Improved Follow-Up Results [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1653?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Recent studies on stent placement of significant stenoses at the origin of the vertebral artery reported excellent immediate results. Long-term outcomes, however, were disappointing due to high restenosis rates and stent breakage. In the present study, we evaluated the application of a short drug-eluting balloon-expandable coronary stent for the endovascular treatment of these frequent lesions.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>In a period of 23 months, 48 patients (12 women, 36 men) with a mean age of 68 years (range, 46&ndash;82 years) harboring 52 significant ostial vertebral artery stenoses underwent treatment with short (8 mm) balloon-expandable paclitaxel-eluting coronary stents. Stents were deployed as closely as possible so that the proximal end was just at the origin of the vertebral artery, with high inflation pressure applied. Patients were under continuous medication with acetylsalicylic acid and clopidogrel before and after the treatment. Follow-up clinical assessment and angiography were performed in all patients.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Periprocedural complications were not encountered. Stenosis severity was reduced from 62 &plusmn; 2% (mean &plusmn; standard error of the mean) preprocedurally to 15 &plusmn; 2% postprocedurally. Follow-up angiography at 7.7 &plusmn; 0.6 months revealed a mean stenosis degree of 24 &plusmn; 3%. None of the patients developed posterior circulation symptoms related to the treated segment during the follow-up period. Recurrent stenosis (&gt;50%) at follow-up was found in 6 (12%) lesions.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Stent placement of significant ostial vertebral artery stenosis by using short drug-eluting stents is safe and yields good midterm patency rates and excellent protection from posterior circulation ischemia.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Vajda, Z., Miloslavski, E., Guthe, T., Fischer, S., Albes, G., Heuschmid, A., Henkes, H.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1715</dc:identifier>
<dc:title><![CDATA[Treatment of Stenoses of Vertebral Artery Origin Using Short Drug-Eluting Coronary Stents: Improved Follow-Up Results [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1656</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1653</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1657?rss=1">
<title><![CDATA[Angiographic and Clinical Outcomes in 200 Consecutive Patients with Cerebral Aneurysm Treated with Hydrogel-Coated Coils [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1657?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Denser coil packing in intracranial aneurysms is believed to result in lower recanalization rates. Hydrogel-coated expandable coils (HydroCoil) improve volumetric packing of aneurysms in animal models and clinical studies, but data from large clinical series are limited. The objective of this retrospective analysis was to analyze immediate and follow-up angiographic results as well as complications in a large consecutive series of patients treated with HydroCoils at a single institution.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Retrospective analysis was performed of periprocedural complications, immediate and follow-up angiograms, and retreatments of the first 200 consecutive intracranial aneurysms treated at Emory University Hospital.</p>
</sec>
<sec><st>RESULTS:</st>
<p>One hundred eighty-seven patients with 200 intracranial aneurysms were treated with HydroCoils during a 3-year period. Immediate angiograms showed complete aneurysmal obliteration in 58.4% of small aneurysms and 42.7% of large aneurysms. Periprocedural complications included early rebleeding and thromboembolic events resulting in permanent neurologic morbidity and mortality in 6% of cases. Follow-up angiography during an average of 16.3 months demonstrated recanalization in 17.7% of small aneurysms and 28.6% of large aneurysms, requiring retreatment in 6.3% and 19.0% of cases, respectively. During the same time period, there was delayed angiographic improvement in aneurysm obliteration in 26.6% of small aneurysms and 26.2% of large aneurysms.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>First-generation HydroCoil treatment of intracranial aneurysms has a favorable rate of recanalization compared with most large series of pure platinum coils with similar complication rates.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Gunnarsson, T., Tong, F.C., Klurfan, P., Cawley, C.M., Dion, J.E.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1691</dc:identifier>
<dc:title><![CDATA[Angiographic and Clinical Outcomes in 200 Consecutive Patients with Cerebral Aneurysm Treated with Hydrogel-Coated Coils [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1664</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1657</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1665?rss=1">
<title><![CDATA[Evaluation of the Occlusion Status of Coiled Intracranial Aneurysms with MR Angiography at 3T: Is Contrast Enhancement Necessary? [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1665?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>MR angiography (MRA) is increasingly used as a noninvasive imaging technique for the follow-up of coiled intracranial aneurysms. However, the need for contrast enhancement has not yet been elucidated. We compared 3D time-of-flight MRA (TOF-MRA) and contrast-enhanced MRA (CE-MRA) at 3T with catheter angiography.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Sixty-seven patients with 72 aneurysms underwent TOF-MRA, CE-MRA, and catheter-angiography 6 months after coiling. Occlusion status on MRA was classified as adequate (complete and neck remnant) or incomplete by 2 independent observers. For TOF-MRA and CE-MRA, interobserver agreement, intermodality agreement, and correlation with angiography were assessed by  statistics.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Catheter-angiography revealed incomplete occlusion in 12 (17%) of the 69 aneurysms; 3 aneurysms were excluded due to MR imaging artifacts. Interobserver agreement was good for CE-MRA ( = 0.77; 95% confidence interval [CI], 0.55&ndash;0.98) and very good for TOF-MRA ( = 0.89; 95% CI, 0.75&ndash;1.00). Correlation of TOF-MRA and CE-MRA with angiography was good. The sensitivity of TOF-MRA and CE-MRA was 75% (95% CI, 43%&ndash;95%); the specificity of TOF-MRA was 98% (95% CI, 91%&ndash;100%) and of CE-MRA, 97% (95% CI, 88%&ndash;100%). All 5 incompletely occluded aneurysms, which were additionally treated, were correctly identified with both MRA techniques. Areas under the receiver operating characteristic curve for TOF-MRA and CE-MRA were 0.90 (95% CI, 0.79&ndash;1.00) and 0.91 (95% CI, 0.79&ndash;1.00). Intermodality agreement between TOF-MRA and CE-MRA was very good ( = 0.83; 95% CI, 0.65&ndash;1.00), with full agreement in 66 (96%) of the 69 aneurysms.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>In this study, TOF-MRA and CE-MRA at 3T were equivalent in evaluating the occlusion status of intracranial aneurysms after coiling. Because TOF-MRA does not involve contrast administration, this method is preferred over CE-MRA.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Sprengers, M.E.S., Schaafsma, J.D., van Rooij, W.J., van den Berg, R., Rinkel, G.J.E., Akkerman, E.M., Ferns, S.P., Majoie, C.B.L.M.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1678</dc:identifier>
<dc:title><![CDATA[Evaluation of the Occlusion Status of Coiled Intracranial Aneurysms with MR Angiography at 3T: Is Contrast Enhancement Necessary? [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1671</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1665</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1672?rss=1">
<title><![CDATA[Intrasinus Catheter-Directed Heparin Infusion in the Treatment of Dural Venous Sinus Thrombosis [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1672?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>In this small series, local intrasinus catheter-directed heparin infusion with or without balloon thrombectomy was safe in the treatment of dural venous sinus thrombosis (DVST). Although systemic anticoagulation (SAC) is the treatment of choice, there is a lack of consensus regarding the best treatment should SAC fail or be contraindicated. We present our institutional experience with 16 patients in whom failure of, or contraindication to, SAC occurred and who subsequently underwent intrasinus catheter-directed heparin infusion with or without balloon thrombectomy.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A retrospective review of 16 patients ranging in age from 14 days to 77 years who had intrasinus catheter-directed heparin infusion was undertaken with 9 male and 7 female patients identified. Of these 16 patients, 4 (25%) had a contraindication to SAC and SAC failed in 12 (75%). Technically successful intrasinus infusion catheter placement was achieved in all 16 patients (100%). Mean duration of infusion was 3.3 days (range, 1&ndash;6 days). Adjunctive balloon thrombectomy was performed in 9 (56.3%) of 16 patients. No procedure-related mortality occurred.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Partial and complete sinus recanalization occurred in 10 (62.5%) of 16 patients and 1 (6.3%) of 16 patients, respectively. There were 3 deaths (18.8%) attributed to disease progression. At most recent clinical follow-up (mean, 9.3 months), 11 (84.6%) of 13 surviving patients were independent, with a modified Rankin Scale (mRS) score of 1 or less.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Local intrasinus catheter-directed heparin infusion with or without adjunctive balloon thrombectomy seems to be a safe and effective treatment of DVST in patients in whom SAC failed or in whom there was a contraindication to SAC. In addition, the risk for symptomatic intracranial hemorrhage may be significantly lower than intrasinus infusion of thrombolytics.</p>
</sec>
]]></description>
<dc:creator><![CDATA[La Barge, D.V., Bishop, F.S., Stevens, E.A., Eskandari, R., Schmidt, R.H., Skalabrin, E.J., Ng, P.P.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:14 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1677</dc:identifier>
<dc:title><![CDATA[Intrasinus Catheter-Directed Heparin Infusion in the Treatment of Dural Venous Sinus Thrombosis [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1678</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1672</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1679?rss=1">
<title><![CDATA[Ethanol Embolization of Auricular Arteriovenous Malformations: Preliminary Results of 17 Cases [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1679?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Because of the relatively rare and extremely varied clinical presentations, arteriovenous malformations (AVMs) involving the auriculae are technically challenging clinical entities to diagnose and, ultimately, manage. The purpose of our study was to present our initial experience of ethanol embolization in a series of 17 patients with auricular AVMs and assess the interim therapeutic outcomes of this method.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Our study group consisted of 17 patients. Transcatheter arterial embolization and/or direct percutaneous puncture embolization were performed. Pure or diluted ethanol was manually injected. Follow-up evaluation was obtained on the basis of physical examination and angiography at 3- to 4-month intervals and telephone questionnaire at 1-month intervals in all patients.</p>
</sec>
<sec><st>RESULTS:</st>
<p>During the 29 ethanol embolization procedures, the amount of ethanol used ranged from 4 to 65 mL. The obliteration of ulceration, hemorrhage, pain, infection, pulsation, and bruit in most of the patients was obtained. The reduction of redness, swelling, and warmth was achieved in all of the patients, and 15 of the patients achieved downstaging of the Schobinger status. According to the angiographic findings, AVMs were devascularized 100% in 3 patients, 76% to 99% in 5 patients, 50% to 75% in 6 patients, and less than 50% in 3 patients. The most common complications were reversible necrosis and blister.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Ethanol embolization has proved efficacious and safe in the treatment of auricular AVMs and has the potential to be accepted as the primary mode of therapy in the management of these lesions.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Zheng, L.Z., Fan, X.D., Zheng, J.W., Su, L.X.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1687</dc:identifier>
<dc:title><![CDATA[Ethanol Embolization of Auricular Arteriovenous Malformations: Preliminary Results of 17 Cases [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1684</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1679</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1685?rss=1">
<title><![CDATA[Neck Injury Is Critical to Elastase-Induced Aneurysm Model [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1685?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>We modified the elastase-induced aneurysm model by use of a simple surgical technique in rabbits. A temporary arcuated aneurysm clip was placed at the origin of the right common carotid artery (RCCA), ascertaining the inner edge of the clip blade on the juncture of the RCCA and right subclavian artery (RSCA), and the elastase-induced aneurysm procedure was undertaken. We found elastase and location of the temporary arcuated aneurysm clip are critical to the success of this aneurysm model.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wang, K., Huang, Q., Hong, B., Xu, Y., Zhao, W., Chen, J., Zhao, R., Liu, J.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1542</dc:identifier>
<dc:title><![CDATA[Neck Injury Is Critical to Elastase-Induced Aneurysm Model [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1687</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1685</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1688?rss=1">
<title><![CDATA[Pedunculated Basilar Terminus Aneurysm with Pseudo-Septation due to Anterior Herniation through a Perforated Membrane of Liliequist [INTERVENTIONAL]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1688?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Septations within cerebral arteries or aneurysms are exceedingly rare in the absence of associated fenestrations. We report an unusual unruptured pedunculated basilar apex aneurysm, with a "pseudoseptation" between the main aneurysmal sac and an anterior compartment, which was, in fact, represented by a perforation in the membrane of Liliequist, permitting anterior aneurysmal herniation into the carotid-chiasmatic cistern. The patient was successfully treated with detachable coils. This case is unusual on 2 accounts: 1) the aneurysm's appearance, and 2) the presence of a large fenestration in the membrane of Liliequist, of which anatomic features are herein reviewed.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Hacein-Bey, L., Varelas, P.N.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1624</dc:identifier>
<dc:title><![CDATA[Pedunculated Basilar Terminus Aneurysm with Pseudo-Septation due to Anterior Herniation through a Perforated Membrane of Liliequist [INTERVENTIONAL]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1690</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1688</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1691?rss=1">
<title><![CDATA[A Case of Spinal Cord Infarction Following Lumbar Transforaminal Epidural Steroid Injection: MR Imaging and Angiographic Findings [SPINE]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1691?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Spinal cord infarction following lumbar transforaminal epidural steroid injection is a rare and devastating complication. We describe the case of a 55-year-old woman who developed spinal cord infarction following right L2-3 transforaminal epidural injection, diagnosed on the basis of clinical and MR imaging findings. Spinal angiography demonstrated occlusion of the right L2 segmental artery with reconstitution of the radicular branch from collaterals. The artery of Adamkeiwicz could not be demonstrated and was presumably occluded by the steroid injection.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lyders, E.M., Morris, P.P.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1567</dc:identifier>
<dc:title><![CDATA[A Case of Spinal Cord Infarction Following Lumbar Transforaminal Epidural Steroid Injection: MR Imaging and Angiographic Findings [SPINE]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1693</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1691</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1694?rss=1">
<title><![CDATA[Susceptibility-Weighted Imaging in the Diagnosis of Early Basal Ganglia Germinoma [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1694?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Germinomas originating from the basal ganglia (BG) are rare. Early diagnosis is important for favorable prognosis, but it is difficult due to the slow clinical course and subtle changes on neuroimaging. The purpose of this study was to evaluate the usefulness of susceptibility-weighted imaging (SWI) in the diagnosis of early BG germinoma.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>From 2006 to 2008, 6 BG germinomas were diagnosed in children at our institution by pathology. Conventional MR imaging and SWI were available in all cases. Clinical, neuroradiologic, and follow-up features were retrospectively studied.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Three cases were classified as early BG germinomas. Conventional MR imaging demonstrated that the tumor size was &lt;10 mm in the largest diameter. The tumors were invisible or showed slight hyperintensity on T1-weighted images (T1WI) and patchy slight hyperintensity on T2-weighted images (T2WI) without mass effect or enhancement. On SWI, the tumors appeared as obvious hypointensity in the globus pallidus and putamen, and the size was larger than that on conventional T1WI and T2WI. The other 3 cases with tumor size &gt;10 mm in largest diameter were classified as late BG germinomas, with tumor necrosis, fluid-fluid levels, and perifocal edema, including 1 case with subependymal spread. On SWI, only the solid portion of the tumors showed hypointensity. No recurrence was noted on follow-up.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>SWI appears to be more sensitive in detecting early BG germinomas than conventional MR imaging. This capability may prove to be useful in future attempts to characterize early BG germinomas.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lou, X., Ma, L., Wang, F.-L., Tang, Z.-P., Huang, H., Cai, Y.-Q., Wong, E.-H.-C.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1696</dc:identifier>
<dc:title><![CDATA[Susceptibility-Weighted Imaging in the Diagnosis of Early Basal Ganglia Germinoma [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1699</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1694</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1700?rss=1">
<title><![CDATA[Fractional Anisotropy-Threshold Dependence in Tract-Based Diffusion Tensor Analysis: Evaluation of the Uncinate Fasciculus in Alzheimer Disease [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1700?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Tract-based analysis can be used to investigate required tracts extracted from other fiber tracts. However, the fractional anisotropy (FA) threshold influences tractography analysis. The current study evaluated the influence of the FA threshold in measuring diffusion tensor parameters for tract-based analysis of the uncinate fasciculus in subjects with Alzheimer disease (AD).</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Subjects included 30 patients with AD and 10 healthy controls. We acquired tractographies of the uncinate fasciculus by using different FA thresholds. We measured mean FA and the apparent diffusion coefficient (ADC) along the uncinate fasciculus for different FA thresholds and evaluated the correlation between diffusion tensor parameters (FA, ADC) and the Mini-Mental State Examination (MMSE) scores.</p>
</sec>
<sec><st>RESULTS:</st>
<p>The uncinate fasciculus showed lower mean FA and higher mean ADC values in cases with more severe AD. A higher FA threshold led to a lower mean ADC value and a higher mean FA value along the uncinate fasciculus, whereas the relative order of measured values according to the severity of AD was not influenced by the FA threshold. An FA threshold of 0.2 showed higher correlation between mean ADC values and MMSE scores. FA thresholds of 0.15 and 0.20 showed higher correlation between mean FA values and MMSE scores.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Appropriate selection of the FA threshold leads to higher correlation between diffusion tensor parameters and the severity of AD. For tract-based analysis of degenerative diseases such as AD, appropriate selection of the FA threshold for tractography is important.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Taoka, T., Morikawa, M., Akashi, T., Miyasaka, T., Nakagawa, H., Kiuchi, K., Kishimoto, T., Kichikawa, K.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1698</dc:identifier>
<dc:title><![CDATA[Fractional Anisotropy-Threshold Dependence in Tract-Based Diffusion Tensor Analysis: Evaluation of the Uncinate Fasciculus in Alzheimer Disease [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1703</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1700</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1704?rss=1">
<title><![CDATA[A New Reference Line for the Brain CT: The Tuberculum Sellae-Occipital Protuberance Line is Parallel to the Anterior/Posterior Commissure Line [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1704?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>CT and MR imaging of the brain have diverged reference lines. Modified Talairach anterior/posterior commissure (ACPC) line is widely accepted as the standard for clinical brain MR imaging, while orbitomeatal line (OML) is used for CT. This study sought to determine an appropriate reference line for brain CT parallel to the ACPC line.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>We measured the angles between the ACPC line and the OML, the line connecting the tuberculum sellae and the internal occipital protuberance (TS-IOP line), and the line connecting the tuberculum sellae and the external occipital protuberance (TS-EOP line) on midsagittal brain MR images of 223 patients. In addition, with the hard palate as the basis, the angles to the ACPC line in the brain MR images and new reference line on the brain CT images from the same patient were measured, and the difference between the 2 angles was calculated in 30 patients. In the same method, the angles to the OML in the brain CT images and the ACPC line on the brain MR images were measured, and their difference was calculated in 30 patients. Then the 2 difference values were compared with verification of the new reference line.</p>
</sec>
<sec><st>RESULTS:</st>
<p>The angles between the ACPC line and both the TS-IOP line (0.0&deg; &plusmn; 4.0&deg;) and the TS-EOP line (0.8&deg; &plusmn; 3.2&deg;) were significantly smaller than the angles between the ACPC line and the OML (&ndash;12.6&deg; &plusmn; 4.2&deg;; <I>P</I> &lt; .05). In actual scanned images, the angle differences between the TS-OP (TS-IOP + TS-EOP) line and the ACPC line (0.3&deg; &plusmn; 4.5&deg;) were statistically smaller than the angles between the OML and the ACPC line (&ndash;6.6&deg; &plusmn; 3.9&deg;; <I>P</I> &lt; .05).</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>TS-OP lines are nearly parallel to the ACPC line.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kim, Y.I., Ahn, K.J., Chung, Y.A., Kim, B.S.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1676</dc:identifier>
<dc:title><![CDATA[A New Reference Line for the Brain CT: The Tuberculum Sellae-Occipital Protuberance Line is Parallel to the Anterior/Posterior Commissure Line [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1708</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1704</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1709?rss=1">
<title><![CDATA[Unilateral Hemispheric Proliferation of Ivy Sign on Fluid-Attenuated Inversion Recovery Images in Moyamoya Disease Correlates Highly with Ipsilateral Hemispheric Decrease of Cerebrovascular Reserve [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1709?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>An ivy sign is considered to represent diffuse leptomeningeal collaterals found on fluid-attenuated inversion recovery (FLAIR) images of patients with Moyamoya disease. We evaluated the correlation between unilateral ivy proliferation in a hemisphere and cerebrovascular hemodynamic status to learn the clinical significance of the ivy sign.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A total of 35 patients with Moyamoya disease were included. Correlation between ivy dominance on FLAIR images and hemodynamic status with use of iodine 123 <I>N</I>-isopropyl-p-iodoamphetamine (<sup>123</sup>I-IMP) single-photon emission CT (SPECT) was evaluated.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Distributional differences of ivy signs between both hemispheres were observed in 22 (64.7%) of 34 patients with a positive ivy sign, all of whom showed decreased vascular reserve/reactivity in the ivy-dominant hemisphere (IDH). The proportion of the stage II (misery perfusion) area to IDH was higher than that in the ivy less-dominant hemisphere (ILDH) in the quantitative analysis. The mean vascular reserve was lower in IDH than ILDH. There were 15 of 22 patients who had bypass surgery on IDH because of transient ischemic attack from ischemia of IDH. Patients with symmetric ivy distributions showed a variety of hemodynamic status. MR angiography (MRA) stage of IDH (2.95 &plusmn; 0.39) was higher compared with ILDH (2.60 &plusmn; 0.50; <I>P</I> &lt; .05). Regional arteriocapillary circulation time ratio in IDH was longer compared with ILDH (<I>P</I> &lt; .05). Ivy proliferation decreased in 10 (55.6%) of 18 patients who underwent bypass surgery during the follow-up period.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Unilateral hemispheric ivy proliferation correlated highly with the existence of an ipsilateral decreased vascular reserve associated with the development of leptomeningeal collaterals in patients with Moyamoya disease.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Kawashima, M., Noguchi, T., Takase, Y., Ootsuka, T., Kido, N., Matsushima, T.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1679</dc:identifier>
<dc:title><![CDATA[Unilateral Hemispheric Proliferation of Ivy Sign on Fluid-Attenuated Inversion Recovery Images in Moyamoya Disease Correlates Highly with Ipsilateral Hemispheric Decrease of Cerebrovascular Reserve [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1716</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1709</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1717?rss=1">
<title><![CDATA[Localization of the Subthalamic Nucleus: Optimization with Susceptibility-Weighted Phase MR Imaging [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1717?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>On clinical MR images, the subthalamic nuclei (STN) are poorly delineated from adjacent structures, impeding safe direct targeting for placement of electrodes in the treatment of Parkinson disease. Susceptibility-weighted MR phase imaging offers improved contrast and spatial resolution at reduced imaging times relative to clinically used T2-weighted spin-echo imaging for STN visualization. Our purpose was to assess STN visibility by using phase imaging, comparing phase and magnitude images obtained concurrently by using susceptibility-weighted imaging (SWI). The goal was to identify an efficient scanning protocol for high-quality phase images of STN.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Seventy-eight SWI scans were acquired at 3T by using different TEs and acceleration factors. STN visibility and delimitation from adjacent structures were scored from 0 (not interpretable) to 5 (excellent). Regression analyses assessed the relationship of STN visibility to scanning parameters</p>
</sec>
<sec><st>RESULTS:</st>
<p>STN were identified at all studied TEs on phase images. Visibility and delimitation of STN were consistently superior on phase images compared with magnitude images. Good visualization (score of &ge;4) of STN on phase imaging occurred at a mean TE of 20.0 ms and a sensitivity encoding (SENSE) of 1.40. Scores of STN visualization on phase images were dependent on SENSE (<I>P</I> &lt; .002) and TE (<I>P</I> &lt; .031). Good delimitation of the STN on phase imaging occurred at a mean TE of 21.6 ms and a SENSE of 1.36.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Visualization and delimitation of STN was superior on phase images and was achieved at 3T in &lt;2.5 minutes. A TE of 20 ms and an acceleration factor of &le;1.5 are recommended to visualize STN by using this method.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Vertinsky, A.T., Coenen, V.A., Lang, D.J., Kolind, S., Honey, C.R., Li, D., Rauscher, A.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1669</dc:identifier>
<dc:title><![CDATA[Localization of the Subthalamic Nucleus: Optimization with Susceptibility-Weighted Phase MR Imaging [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1724</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1717</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1725?rss=1">
<title><![CDATA[Cerebellar Lesions in Multiple System Atrophy: Postmortem MR Imaging-Pathologic Correlations [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1725?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Cerebellar atrophy and white matter T2-hyperintensities have been characterized as cerebellar lesions of multiple system atrophy (MSA). The aim of the study was to correlate MR images with histologic findings in cerebellar lesions of MSA.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Postmortem T2-weighted images using 1.5T were compared with histologic findings in 7 postmortem-proved cases with MSA. The MR imaging findings in the cerebellar cortices and deep white matter dentate nucleus regions were compared with their histologic findings in each case.</p>
</sec>
<sec><st>RESULTS:</st>
<p>We detected 3 types of cerebellar changes: type 1, no apparent atrophy or signal-intensity changes; type 2, cerebellar atrophy and inhomogeneous (patchy and/or confluent) cerebellar white matter hyperintensities; and type 3, cerebellar atrophy and diffuse white matter hyperintensities. Hypointensities were seen in the dentate nucleus regions. Atrophy of the cerebellar white matter was more severe than that of cerebellar cortices, and this anatomy was well depicted on coronal images. Histologically, degeneration was more severe in the cerebellar white matter than in the cerebellar cortices. Hyperintensities in the cerebellar white matter showed loss of myelinated fibers and gliosis. Hypointensities in the dentate nucleus regions revealed diffuse ferritin deposition in preserved dentate nuclei and white matter both around and within the nuclei.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Hyperintensities in the cerebellar white matter reflect degenerated white matter associated with loss of myelinated fibers and gliosis, whereas hypointensities in the dentate nucleus regions reflect diffuse ferritin deposition in preserved dentate nuclei and white matter around and within the nuclei. Degeneration is more severe in the cerebellar white matter than in the cerebellar cortices.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Matsusue, E., Fujii, S., Kanasaki, Y., Kaminou, T., Ohama, E., Ogawa, T.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1662</dc:identifier>
<dc:title><![CDATA[Cerebellar Lesions in Multiple System Atrophy: Postmortem MR Imaging-Pathologic Correlations [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1730</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1725</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1731?rss=1">
<title><![CDATA[Regional White Matter Atrophy-Based Classification of Multiple Sclerosis in Cross-Sectional and Longitudinal Data [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1731?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>The different clinical subtypes of multiple sclerosis (MS) may reflect underlying differences in affected neuroanatomic regions. Our aim was to analyze the effectiveness of jointly using the inferior subolivary medulla oblongata volume (MOV) and the cross-sectional area of the corpus callosum in distinguishing patients with relapsing-remitting multiple sclerosis (RRMS), secondary-progressive multiple sclerosis (SPMS), and primary-progressive multiple sclerosis (PPMS).</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>We analyzed a cross-sectional dataset of 64 patients (30 RRMS, 14 SPMS, 20 PPMS) and a separate longitudinal dataset of 25 patients (114 MR imaging examinations). Twelve patients in the longitudinal dataset had converted from RRMS to SPMS. For all images, the MOV and corpus callosum were delineated manually and the corpus callosum was parcellated into 5 segments. Patients from the cross-sectional dataset were classified as RRMS, SPMS, or PPMS by using a decision tree algorithm with the following input features: brain parenchymal fraction, age, disease duration, MOV, total corpus callosum area and areas of 5 segments of the corpus callosum. To test the robustness of the classification technique, we applied the results derived from the cross-sectional analysis to the longitudinal dataset.</p>
</sec>
<sec><st>RESULTS:</st>
<p>MOV and central corpus callosum segment area were the 2 features retained by the decision tree. Patients with MOV &gt;0.94 cm<sup>3</sup> were classified as having RRMS. Patients with progressive MS were further subclassified as having SPMS if the central corpus callosum segment area was &lt;55.12 mm<sup>2</sup>, and as having PPMS otherwise. In the cross-sectional dataset, 51/64 (80%) patients were correctly classified. For the longitudinal dataset, 88/114 (77%) patient time points were correctly classified as RRMS or SPMS.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Classification techniques revealed differences in affected neuroanatomic regions in subtypes of multiple sclerosis. The combination of central corpus callosum segment area and MOV provides good discrimination among patients with RRMS, SPMS, and PPMS.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Sampat, M.P., Berger, A.M., Healy, B.C., Hildenbrand, P., Vass, J., Meier, D.S., Chitnis, T., Weiner, H.L., Bakshi, R., Guttmann, C.R.G.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1659</dc:identifier>
<dc:title><![CDATA[Regional White Matter Atrophy-Based Classification of Multiple Sclerosis in Cross-Sectional and Longitudinal Data [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1739</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1731</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1740?rss=1">
<title><![CDATA[Side Matters: Diffusion Tensor Imaging Tractography in Left and Right Temporal Lobe Epilepsy [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1740?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Noninvasive imaging plays a pivotal role in lateralization of the seizure focus in presurgical patients with temporal lobe epilepsy (TLE). Our goal was to evaluate the utility of diffusion tensor imaging (DTI) tractography in TLE.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Twenty-one patients with TLE (11 right, 10 left TLE) and 21 controls were enrolled. A 1.5T MR imaging scanner was used to obtain 51 diffusion-gradient-direction images per subject. Eight pairs of white matter fiber tracts were traced, and fiber tract fractional anisotropy (FA) was calculated and compared with controls. Fiber tract FA asymmetry and discriminant function analysis were evaluated in all subjects and fiber tracts respectively.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Compared with controls, patients with TLE demonstrated decreased FA in 5 ipsilateral fiber tracts. Patients with left TLE had 6 ipsilateral and 4 contralateral fiber tracts with decreased FA. Patients with right TLE had 4 ipsilateral but no contralateral tracts with decreased FA compared with controls. Right-sided FA asymmetry was demonstrated in patients with right TLE for 5 fiber tracts, and left-sided asymmetry, for patients with left TLE for 1 fiber tract. Discriminant function analysis correctly categorized patients into left-versus-right TLE in 90% of all cases (100% correct in all patients without hippocampal sclerosis) by using uncinate fasciculus and parahippocampal fiber tracts.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>We found widespread reductions in fiber tract FA in patients with TLE, which were most pronounced ipsilateral to the seizure focus. Patients with left TLE had greater, more diffuse changes, whereas patients with right TLE showed changes that were primarily ipsilateral. Disease was lateralized to a high degree independent of identifiable hippocampal pathology noted on conventional MR imaging.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Ahmadi, M.E., Hagler, D.J., McDonald, C.R., Tecoma, E.S., Iragui, V.J., Dale, A.M., Halgren, E.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1650</dc:identifier>
<dc:title><![CDATA[Side Matters: Diffusion Tensor Imaging Tractography in Left and Right Temporal Lobe Epilepsy [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1747</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1740</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1748?rss=1">
<title><![CDATA[Sphenoidal Electrode Placement Using Biplane Fluoroscopy and Rotational Flat Panel CT Imaging [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1748?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Assessment of otherwise occult seizure foci arising from the anterior mesial temporal region occasionally necessitates placement of sphenoidal electrodes (SEs). This minimally invasive procedure is often performed without imaging guidance; however, more precise lead positioning with a reduced risk of complications has been described with fluoroscopic guidance. We describe the added value of rotational flat panel CT imaging for precise anatomic localization of the SE tip in relation to the foramen ovale.</p>
</sec>
]]></description>
<dc:creator><![CDATA[La Barge, D.V., Ng, P.P., Stevens, E.A.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1578</dc:identifier>
<dc:title><![CDATA[Sphenoidal Electrode Placement Using Biplane Fluoroscopy and Rotational Flat Panel CT Imaging [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1750</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1748</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1751?rss=1">
<title><![CDATA[Ipilimumab-Induced Hypophysitis: MR Imaging Findings [BRAIN]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1751?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Ipilimumab is a promising new immunotherapeutic antineoplastic agent with clinical activity in the treatment of metastatic melanoma and renal cell carcinoma. With advances in immunotherapy, however, a host of new side effects related to the mechanism of action of these drugs has appeared. At our institution, 3 patients presented with hypophysitis, which was attributed to an autoimmune process based on the documented relationship of the drug to other autoimmune phenomena and significant and rapid improvement with discontinuation of the drug and addition of steroids. We present the imaging findings in 3 patients with presumed ipilimumab-induced hypophysitis.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Carpenter, K.J., Murtagh, R.D., Lilienfeld, H., Weber, J., Murtagh, F.R.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1623</dc:identifier>
<dc:title><![CDATA[Ipilimumab-Induced Hypophysitis: MR Imaging Findings [BRAIN]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1753</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1751</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1754?rss=1">
<title><![CDATA[Comparison of Image Quality and Radiation Dose between Fixed Tube Current and Combined Automatic Tube Current Modulation in Craniocervical CT Angiography [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1754?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>The combined automatic tube current modulation (ATCM) technique adapts and modulates the x-ray tube current in the <I>x-y-z</I> axis according to the patient's individual anatomy. We compared image quality and radiation dose of the combined ATCM technique with those of a fixed tube current (FTC) technique in craniocervical CT angiography performed with a 64-section multidetector row CT (MDCT) system.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A retrospective review of craniocervical CT angiograms (CTAs) by using combined ATCM (<I>n</I> = 25) and FTC techniques (<I>n</I> = 25) was performed. Other CTA parameters, such as kilovolt (peak), matrix size, FOV, section thickness, pitch, contrast agent, and contrast injection techniques, were held constant. We recorded objective image noise in the muscles at 2 anatomic levels: radiation exposure doses (CT dose index volume and dose-length product); and subjective image quality parameters, such as vascular delineation of various arterial vessels, visibility of small arterial detail, image artifacts, and certainty of diagnosis. The Mann-Whitney <I>U</I> test was used for statistical analysis.</p>
</sec>
<sec><st>RESULTS:</st>
<p>No significant difference was detected in subjective image quality parameters between the FTC and combined ATCM techniques. Most subjects in both study groups (49/50, 98%) had acceptable subjective artifacts. The objective image noise values at shoulder level did not show a significant difference, but the noise value at the upper neck was higher with the combined ATCM (<I>P</I> &lt; .05) technique. Significant reduction in radiation dose (18% reduction) was noted with the combined ATCM technique (<I>P</I> &lt; .05).</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The combined ATCM technique for craniocervical CTA performed at 64-section MDCT substantially reduced radiation exposure dose but maintained diagnostic image quality.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lee, E.J., Lee, S.K., Agid, R., Howard, P., Bae, J.M., terBrugge, K.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1675</dc:identifier>
<dc:title><![CDATA[Comparison of Image Quality and Radiation Dose between Fixed Tube Current and Combined Automatic Tube Current Modulation in Craniocervical CT Angiography [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1759</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1754</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1760?rss=1">
<title><![CDATA[Is CT Still Useful in the Study Protocol of Retinoblastoma? [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1760?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Intralesional calcium deposition is considered a key element for differentiating retinoblastoma from simulating lesions. Our aim was to assess whether MR imaging associated with ophthalmologic investigations (ophthalmoscopy and ultrasonography) could replace CT in the detection of diagnostic intralesional calcifications in retinoblastoma.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Ophthalmoscopic findings, MR images, CT scans, and histologic examination of 28 retinoblastomas from 23 consecutive children (11 males, 12 females; age range at admission, 1&ndash;35 months; mean age, 11 months; median age, 9 months) were retrospectively evaluated. Ultrasonography was performed in 18 patients with 21 retinoblastomas. MR imaging included T2-weighted spin-echo and gradient-echo images, fluid-attenuated inversion recovery images, and T1-weighted spin-echo images with and without contrast enhancement. Clinical data were integrated with MR imaging data to evaluate the utility of both approaches to discover calcifications; particularly, a correlation between intralesional signal-intensity void spots on MR imaging and hyperattenuating areas on CT scans was performed.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Ophthalmoscopy detected calcifications in 12 of 28 eyes (42.85%). Ultrasonography detected calcifications in 20 of 21 eyes (95.23%). CT showed hyperattenuating intralesional areas consistent with calcifications in 27 of 28 eyes (96.42%). MR imaging showed intralesional signal-intensity void spots in 25 of 28 eyes (89.28%). All spots detected with MR imaging matched the presence of calcifications on CT scans. Gradient-echo T2*-weighted and fast spin-echo T2-weighted images showed the highest degree of correlation with CT. When we put together ophthalmoscopy, ultrasonography, and MR imaging data, no calcifications detected on CT were missed, and the differential diagnosis was thorough.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>A combination of clinical data and MR images may remove potentially harmful ionizing radiation from the study protocol of retinoblastoma.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Galluzzi, P., Hadjistilianou, T., Cerase, A., De Francesco, S., Toti, P., Venturi, C.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1716</dc:identifier>
<dc:title><![CDATA[Is CT Still Useful in the Study Protocol of Retinoblastoma? [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1765</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1760</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1766?rss=1">
<title><![CDATA[A Radiologic Score to Distinguish Autoimmune Hypophysitis from Nonsecreting Pituitary Adenoma Preoperatively [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1766?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Autoimmune hypophysitis (AH) mimics the more common nonsecreting pituitary adenomas and can be diagnosed with certainty only histologically. Approximately 40% of patients with AH are still misdiagnosed as having pituitary macroadenoma and undergo unnecessary surgery. MR imaging is currently the best noninvasive diagnostic tool to differentiate AH from nonsecreting adenomas, though no single radiologic sign is diagnostically accurate. The purpose of this study was to develop a scoring system that summarizes numerous MR imaging signs to increase the probability of diagnosing AH before surgery.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>This was a case-control study of 402 patients, which compared the presurgical pituitary MR imaging features of patients with nonsecreting pituitary adenoma and controls with AH. MR images were compared on the basis of 16 morphologic features besides sex, age, and relation to pregnancy.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Only 2 of the 19 proposed features tested lacked prognostic value. When the other 17 predictors were analyzed jointly in a multiple logistic regression model, 8 (relation to pregnancy, pituitary mass volume and symmetry, signal intensity and signal intensity homogeneity after gadolinium administration, posterior pituitary bright spot presence, stalk size, and mucosal swelling) remained significant predictors of a correct classification. The diagnostic score had a global performance of 0.9917 and correctly classified 97% of the patients, with a sensitivity of 92%, a specificity of 99%, a positive predictive value of 97%, and a negative predictive value of 97% for the diagnosis of AH.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>This new radiologic score could be integrated into the management of patients with AH, who derive greater benefit from medical as opposed to surgical treatment.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Gutenberg, A., Larsen, J., Lupi, I., Rohde, V., Caturegli, P.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1714</dc:identifier>
<dc:title><![CDATA[A Radiologic Score to Distinguish Autoimmune Hypophysitis from Nonsecreting Pituitary Adenoma Preoperatively [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1772</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1766</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1773?rss=1">
<title><![CDATA[Diffusion Tensor Imaging of the Subcortical Auditory Tract in Subjects with Congenital Cochlear Nerve Deficiency [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1773?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Cochlear nerve deficiency (CND), including aplasia and hypoplasia, is a rare cause of congenital hearing loss. The purpose of this study was to evaluate the neuronal integrity of the subcortical auditory pathway in subjects with CND by diffusion tensor MR imaging (DTI).</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Twelve subjects with unilateral congenital CND were included in this prospective study. Twelve normal-hearing subjects served as controls. DTIs were acquired from these subjects on a 3T MR imaging scanner. Several indices including axial diffusivity (<SUB>||</SUB>), radial diffusivity (<SUB></SUB>), mean diffusivity (MD), and fractional anisotropy (FA) along the auditory pathway were extracted. Two regions of interest were selected bilaterally for evaluation: the lateral lemniscus (LL) and inferior colliculus (IC). The mean values of <SUB>||</SUB>, <SUB></SUB>, MD, and FA at both regions of interest were compared between the ipsilateral and contralateral sides of subjects with CND with those in the control group.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Significant decrease of FA and increase of MD on both the ipsilateral and contralateral sides of patients with CND as compared with normal subjects in both LL and IC were found. The decrease of FA was due to the increase of <SUB></SUB>, whereas <SUB>||</SUB> remained unchanged.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The maintained axial diffusion implied that the orientation of neural fibers along the subcortical auditory pathway in subjects with unilateral CND is intact. However, the reduction in FA and increase in <SUB></SUB> on both the ipsilateral and contralateral sides might be attributed to axonal loss and/or demyelination of the subcortical auditory tract in these subjects.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Wu, C.-M., Ng, S.-H., Wang, J.-J., Liu, T.-C.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1681</dc:identifier>
<dc:title><![CDATA[Diffusion Tensor Imaging of the Subcortical Auditory Tract in Subjects with Congenital Cochlear Nerve Deficiency [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1777</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1773</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1778?rss=1">
<title><![CDATA[MR Imaging Features of Acquired Brown Syndrome [HEAD AND NECK]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1778?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Brown syndrome describes the inability of a patient to perform an upward gaze while the eye is adducted due to an abnormality of the superior oblique tendon sheath complex. Use of CT in diagnosing the condition has been reported; however, the use of MR imaging has not. We describe a unique case of Brown syndrome in which the initial CT findings were normal, but MR imaging revealed the abnormality. Key imaging features are illustrated.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Currie, S., Goddard, T.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1591</dc:identifier>
<dc:title><![CDATA[MR Imaging Features of Acquired Brown Syndrome [HEAD AND NECK]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1779</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1778</prism:startingPage>
<prism:section>HEAD AND NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1780?rss=1">
<title><![CDATA[Maturation of Thalamic Radiations between 34 and 41 Weeks' Gestation: A Combined Voxel-Based Study and Probabilistic Tractography with Diffusion Tensor Imaging [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1780?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>This study aimed to investigate brain maturation along gestational age with diffusion tensor imaging in healthy preterm and term neonates. Therefore, a voxel-based study of fractional anisotropy (FA) and mean diffusivity (D<SUB>av</SUB>) was performed to reveal the brain regions experiencing microstructural changes with age. With tractography, the authors intended to identify which fiber tracts were included in these significant voxels.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>There were 22 healthy preterm and 6 healthy term infants who underwent MR imaging between 34 and 41 weeks of gestation. A statistical parametric approach was used to evidence the effect of age on regional distribution of FA and D<SUB>av</SUB> values. The fiber tracts suspected to be included in the significant clusters of voxels were identified with neuroanatomy and tractography atlases, reconstructed with probabilistic tractography, and superimposed on the parametric maps.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Parametric analysis showed that FA increases with age in the subcortical projections from the frontal (motor and premotor areas) and parietal cortices, the centrum semiovale, the anterior and posterior arms of the internal capsules, the optic radiations, the corpus callosum, and the thalami (<I>P</I> &lt; .05, corrected). Superimposition of the parametric maps on tractography showed that the corticospinal tract (CST); the callosal radiations (CR); and the superior, anterior, and posterior thalamic radiations were included in the significant voxels. No statistically significant results were found for D<SUB>av</SUB> maps.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>These results highlight that, besides the already-evidenced FA increase in the CST and CR, the thalami and the thalamic radiations experience microstructural changes in the early development of the human brain.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Aeby, A., Liu, Y., De Tiege, X., Denolin, V., David, P., Baleriaux, D., Kavec, M., Metens, T., Van Bogaert, P.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1660</dc:identifier>
<dc:title><![CDATA[Maturation of Thalamic Radiations between 34 and 41 Weeks' Gestation: A Combined Voxel-Based Study and Probabilistic Tractography with Diffusion Tensor Imaging [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1786</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1780</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1787?rss=1">
<title><![CDATA[In Utero Eye Development Documented by Fetal MR Imaging [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1787?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>To date, very limited attention has been given to ocular abnormalities or growth parameters detected by fetal MR imaging. Our objective was to retrospectively determine the relationship between different parameters of eye development and estimated gestational age in the human fetus by use of fetal MR imaging.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>A retrospective study was performed to measure the transverse diameter, interocular distance, and lens diameter of the globes of 127 fetuses who had a morphologically normal central nervous system. Multiple single-shot T2 fast spin-echo images were obtained with a 1.5T magnet by use of contiguous 3-mm intervals in at least 2 orthogonal planes. Loess curves were fitted to explore the relationship between gestational age and each of the 3 measurements of interest. Different models were compared statistically to determine the model of best fit.</p>
</sec>
<sec><st>RESULTS:</st>
<p>For each variable of interest, the "best" model of eye growth was a quadratic function. Specifically, lens growth seems to plateau after 36 weeks of gestation, interocular distance plateaus after 36 weeks of gestation, and globe growth plateaus after 42 weeks of gestation.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>The lens, orbit, and interocular distance growth of the fetus can be demonstrated on fetal MR imaging. All 3 measurements suggest a quadratic model of growth, which indicates slowing of growth toward the end of gestation.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Paquette, L.B., Jackson, H.A., Tavare, C.J., Miller, D.A., Panigrahy, A.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1664</dc:identifier>
<dc:title><![CDATA[In Utero Eye Development Documented by Fetal MR Imaging [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1791</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1787</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1792?rss=1">
<title><![CDATA[Anisotropic Diffusion Properties in Infants with Hydrocephalus: A Diffusion Tensor Imaging Study [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1792?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Diffusion tensor imaging (DTI) can noninvasively detect in vivo white matter (WM) abnormalities on the basis of anisotropic diffusion properties. We analyzed DTI data retrospectively to quantify the abnormalities in different WM regions in children with hydrocephalus during early infancy.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>Seventeen infants diagnosed with hydrocephalus (age range, 0.13&ndash;16.14 months) were evaluated with DTI and compared with 17 closely age-matched healthy children (age range, 0.20&ndash;16.11 months). Fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity, and radial diffusivity values in 5 regions of interest (ROIs) in the corpus callosum and internal capsule were measured and compared. The correlation between FA and age was also studied and compared by ROI between the 2 study groups.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Infants with hydrocephalus had significantly lower FA, higher MD, and higher radial diffusivity values for all 3 ROIs in the corpus callosum, but not for the 2 ROIs in the internal capsule. In infants with hydrocephalus, the increase of FA with age during normal development was absent in the corpus callosum but was still preserved in the internal capsule. There was also a significant difference in the frequency of occurrence of abnormal FA values in the corpus callosum and internal capsule.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>This retrospective DTI study demonstrated significant WM abnormalities in infants with hydrocephalus in both the corpus callosum and internal capsule. The results also showed evidence that the impact of hydrocephalus on WM was different in the corpus callosum and internal capsule.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Yuan, W., Mangano, F.T., Air, E.L., Holland, S.K., Jones, B.V., Altaye, M., Bierbrauer, K.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1663</dc:identifier>
<dc:title><![CDATA[Anisotropic Diffusion Properties in Infants with Hydrocephalus: A Diffusion Tensor Imaging Study [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1798</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1792</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1799?rss=1">
<title><![CDATA[Normative Apparent Diffusion Coefficient Values in the Developing Fetal Brain [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1799?rss=1</link>
<description><![CDATA[
<sec><st>BACKGROUND AND PURPOSE:</st>
<p>Previous studies of diffusion-weighted imaging (DWI) in fetuses are limited. Because of the need for normative data for comparison with young fetuses and preterm neonates with suspected brain abnormalities, we studied apparent diffusion coefficient (ADC) values in a population of singleton, nonsedated, healthy fetuses.</p>
</sec>
<sec><st>MATERIALS AND METHODS:</st>
<p>DWI was performed in 28 singleton nonsedated fetuses with normal or questionably abnormal results on sonography and normal fetal MR imaging results; 10 fetuses also had a second fetal MR imaging, which included DWI. ADC values in the periatrial white matter (WM), frontal WM, thalamus, basal ganglia, cerebellum, and pons were plotted against gestational age and analyzed with linear regression. We compared mean ADC in different regions using the Tukey Honestly Significant Difference test. We also compared rates of decline in ADC with increasing gestational age across different areas by using the <I>t</I> test with multiple comparisons correction. Neurodevelopmental outcome was assessed.</p>
</sec>
<sec><st>RESULTS:</st>
<p>Median gestational age was 24.28 weeks (range, 21&ndash;33.43 weeks). Results of all fetal MR imaging examinations were normal, including 1 fetus with a normal variant of a cavum velum interpositum. ADC values were highest in the frontal and periatrial WM and lowest in the thalamus and pons. ADC declined with increasing gestational age in periatrial WM (<I>P</I> = .0003), thalamus (<I>P</I> &lt; .0001), basal ganglia (<I>P</I> = .0035), cerebellum (<I>P</I> &lt; .0001), and pons (<I>P</I> = .024). Frontal WM ADC did not significantly change with gestational age. ADC declined fastest in the cerebellum, followed by the thalamus.</p>
</sec>
<sec><st>CONCLUSIONS:</st>
<p>Regional differences in nonsedated fetal ADC values and their evolution with gestational age likely reflect differences in brain maturation and are similar to published data in premature neonates.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Schneider, M.M., Berman, J.I., Baumer, F.M., Glass, H.C., Jeng, S., Jeremy, R.J., Esch, M., Biran, V., Barkovich, A.J., Studholme, C., Xu, D., Glenn, O.A.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1661</dc:identifier>
<dc:title><![CDATA[Normative Apparent Diffusion Coefficient Values in the Developing Fetal Brain [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1803</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1799</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/30/9/1804?rss=1">
<title><![CDATA[The Rare Third Branchial Cleft Cyst [PEDIATRICS]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/9/1804?rss=1</link>
<description><![CDATA[
<sec><st>SUMMARY:</st>
<p>Third branchial cleft cysts (BCCs) are rare entities that represent abnormal persistence of the branchial apparatus. On CT examination, these cysts appear as homogeneous low-attenuation masses with well-circumscribed margins; on MR imaging, they demonstrate variable signal intensity on T1-weighted images and are hyperintense relative to muscle on T2-weighted images. Definitive treatment is surgical excision. We present a case of a third BCC and describe its diagnosis and treatment.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Joshi, M.J., Provenzano, M.J., Smith, R.J.H., Sato, Y., Smoker, W.R.K.]]></dc:creator>
<dc:date>Thu, 08 Oct 2009 10:02:15 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1627</dc:identifier>
<dc:title><![CDATA[The Rare Third Branchial Cleft Cyst [PEDIATRICS]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>1806</prism:endingPage>
<prism:publicationDate>2009-10-01</prism:publicationDate>
<prism:startingPage>1804</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
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<title><![CDATA[Percutaneous Vertebroplasty [INTRODUCTION]]]></title>
<link>http://www.ajnr.org/cgi/content/full/30/suppl_1/S2?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Jensen, M.E., Hirsch, J.A.]]></dc:creator>
<dc:date>Mon, 28 Sep 2009 09:34:09 PDT</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1920</dc:identifier>
<dc:title><![CDATA[Percutaneous Vertebroplasty [INTRODUCTION]]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>suppl 1</prism:number>
<prism:volume>30</prism:volume>
<prism:endingPage>S2</prism:endingPage>
<prism:publicationDate>2009-09-01</prism:publicationDate>
<prism:startingPage>S2</prism:startingPage>
<prism:section>INTRODUCTION</prism:section>
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