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<title>American Journal of Neuroradiology</title>
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<title><![CDATA[[OBITUARY] Pierre Lasjaunias]]></title>
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<dc:creator><![CDATA[Picard, L.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1342</dc:identifier>
<dc:title><![CDATA[[OBITUARY] Pierre Lasjaunias]]></dc:title>
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<prism:number>10</prism:number>
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<title><![CDATA[[LETTERS] Diagnostic Criteria for Spontaneous Spinal CSF Leaks and Intracranial Hypotension]]></title>
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<dc:creator><![CDATA[Albayram, S., Ozer, H., Kara, B.]]></dc:creator>
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<dc:identifier>info:doi/10.3174/ajnr.A1156</dc:identifier>
<dc:title><![CDATA[[LETTERS] Diagnostic Criteria for Spontaneous Spinal CSF Leaks and Intracranial Hypotension]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
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<title><![CDATA[[LETTERS] Reply:]]></title>
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<dc:creator><![CDATA[Schievink, W.I.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1174</dc:identifier>
<dc:title><![CDATA[[LETTERS] Reply:]]></dc:title>
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<prism:number>10</prism:number>
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<title><![CDATA[[LETTERS] Technetium Tc99m Tetrofosmin Single-Photon Emission CT for the Assessment of Glioma Proliferation]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/e96?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Alexiou, G.A., Polyzoidis, K.S., Voulgaris, S., Tsiouris, S., Fotopoulos, A.D., Kyritsis, A.P.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1183</dc:identifier>
<dc:title><![CDATA[[LETTERS] Technetium Tc99m Tetrofosmin Single-Photon Emission CT for the Assessment of Glioma Proliferation]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
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<title><![CDATA[[LETTERS] Acute Reversal of Clopidogrel-Related Platelet Inhibition Using Methyl Prednisolone in a Patient with Intracranial Hemorrhage]]></title>
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<description><![CDATA[]]></description>
<dc:creator><![CDATA[Qureshi, A.I., Suri, M.F.K.]]></dc:creator>
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<dc:identifier>info:doi/10.3174/ajnr.A1297</dc:identifier>
<dc:title><![CDATA[[LETTERS] Acute Reversal of Clopidogrel-Related Platelet Inhibition Using Methyl Prednisolone in a Patient with Intracranial Hemorrhage]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
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<title><![CDATA[[LETTERS] Ruptured Intracranial Aneurysm Treatment Outcomes]]></title>
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<description><![CDATA[]]></description>
<dc:creator><![CDATA[Bansal, A., Derdeyn, C.P.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
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<dc:title><![CDATA[[LETTERS] Ruptured Intracranial Aneurysm Treatment Outcomes]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
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<title><![CDATA[[LETTERS] Reply:]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/e99?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Natarajan, S.K., Sekhar, L.N.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1199</dc:identifier>
<dc:title><![CDATA[[LETTERS] Reply:]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
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<title><![CDATA[[BOOK REVIEWS] Neuropsychiatric Disorders: An Integrative Approach]]></title>
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<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
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<dc:identifier>info:doi/10.3174/ajnr.A1048</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Neuropsychiatric Disorders: An Integrative Approach]]></dc:title>
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<prism:number>10</prism:number>
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<title><![CDATA[[BOOK REVIEWS] Imaging the Mind: Neuroimaging Clinics of North America]]></title>
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<dc:creator><![CDATA[]]></dc:creator>
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<dc:identifier>info:doi/10.3174/ajnr.A1053</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Imaging the Mind: Neuroimaging Clinics of North America]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
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<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/e103?rss=1">
<title><![CDATA[[BOOK REVIEWS] Radiotherapy for Non-Malignant Disorders]]></title>
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<dc:identifier>info:doi/10.3174/ajnr.A1054</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Radiotherapy for Non-Malignant Disorders]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
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<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/e104?rss=1">
<title><![CDATA[[BOOK REVIEWS] Neuropathology Review, 2nd ed.]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/e104?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1085</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Neuropathology Review, 2nd ed.]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e104</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>e104</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/e105?rss=1">
<title><![CDATA[[BOOK REVIEWS] BOOKS RECEIVED]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/e105?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:title><![CDATA[[BOOK REVIEWS] BOOKS RECEIVED]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e105</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>e105</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/e106?rss=1">
<title><![CDATA[[ERRATA] Erratum]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/e106?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1341</dc:identifier>
<dc:title><![CDATA[[ERRATA] Erratum]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e106</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>e106</prism:startingPage>
<prism:section>ERRATA</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/e107?rss=1">
<title><![CDATA[[ERRATA] Erratum]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/e107?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1343</dc:identifier>
<dc:title><![CDATA[[ERRATA] Erratum]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e107</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>e107</prism:startingPage>
<prism:section>ERRATA</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1805?rss=1">
<title><![CDATA[[EDITORIALS] A New Open Access Option from the American Journal of Neuroradiology]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1805?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Castillo, M.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1248</dc:identifier>
<dc:title><![CDATA[[EDITORIALS] A New Open Access Option from the American Journal of Neuroradiology]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1805</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1805</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1806?rss=1">
<title><![CDATA[[REVIEW ARTICLES] Interventional Neuroradiology of the Head and Neck]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1806?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Interventional neuroradiology procedures are a valuable asset in the diagnosis, treatment, and surgical management of various disorders affecting the extracranial head and neck. A detailed understanding of cross-sectional and vascular anatomy and an awareness of potential collateral pathways between extracranial and intracranial vessels are essential for ensuring safe and successful procedures. With the use of high-quality imaging and a meticulous technique, the incidence of major complications is extremely low.</P>
]]></description>
<dc:creator><![CDATA[Gandhi, D., Gemmete, J.J., Ansari, S.A., Gujar, S.K., Mukherji, S.K.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1211</dc:identifier>
<dc:title><![CDATA[[REVIEW ARTICLES] Interventional Neuroradiology of the Head and Neck]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1815</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1806</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1816?rss=1">
<title><![CDATA[[REVIEW ARTICLES] Osteoporosis Primer for the Vertebroplasty Practitioner: Expanding the Focus Beyond Needles and Cement]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1816?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Osteoporosis is a common cause of vertebral compression fractures. Although vertebroplasty is used to treat the pain, the risk of additional compression fractures is very high in these patients. Adequate evaluation and management of the underlying osteoporosis is critical to reducing the risk of subsequent fractures. Such an evaluation involves understanding the underlying physiology of osteoporosis and the role of calcium, vitamin D, prescription medication, and lifestyle changes. This brief review is intended to familiarize neuroradiologists with these aspects so they can advise patients about optimizing fracture risk reduction.</P>
]]></description>
<dc:creator><![CDATA[Kearns, A.E., Kallmes, D.F.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1176</dc:identifier>
<dc:title><![CDATA[[REVIEW ARTICLES] Osteoporosis Primer for the Vertebroplasty Practitioner: Expanding the Focus Beyond Needles and Cement]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1822</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1816</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1823?rss=1">
<title><![CDATA[[RESEARCH PERSPECTIVES] Imaging Preventable Infarction in Patients with Acute Ischemic Stroke]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1823?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> One of the goals of neuroimaging in acute ischemic stroke is to identify those patients whose outcome will be improved by therapeutic intervention. This article will discuss the design, analysis, and interpretation of clinical research studies carried out to establish the accuracy and clinical value of neuroimaging to select such patients.</P>
]]></description>
<dc:creator><![CDATA[Powers, W.J.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1330</dc:identifier>
<dc:title><![CDATA[[RESEARCH PERSPECTIVES] Imaging Preventable Infarction in Patients with Acute Ischemic Stroke]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1825</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1823</prism:startingPage>
<prism:section>RESEARCH PERSPECTIVES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1826?rss=1">
<title><![CDATA[[BRAIN] Renal Safety of CT Angiography and Perfusion Imaging in the Emergency Evaluation of Acute Stroke]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1826?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Multimodal CT imaging with contrast-enhanced CT angiography (CTA) and CT perfusion (CTP) is increasingly being used to guide emergency management of acute stroke. However, little has been reported about the safety of intravenous contrast administration associated with these studies in the acute stroke population, including cases in which baseline creatinine values are unknown. We investigated the incidence of contrast-induced nephropathy (CIN), defined as a 25% or more increase in baseline creatinine levels within 72 hours of contrast administration and chronic kidney disease in patients receiving CTA&plusmn;CTP at our regional stroke center.</P>
<P><B>MATERIALS AND METHODS:</B> We analyzed 198 patients who underwent contrast CT studies for evaluation of acute ischemic or hemorrhagic stroke at our center (2003&ndash;2007). Through retrospective chart abstraction, we analyzed serial creatinine levels (baseline to day 3) and later values (&ge;day 4) where available. The incidences of CIN and/or chronic kidney disease were documented. After power analysis, CIN and non-CIN groups were compared by using the unpaired <I>t</I> test, Wilcoxon rank sum test, or Fisher exact test.</P>
<P><B>RESULTS:</B> None of the 198 patients developed chronic kidney disease or required dialysis. Of 175 patients with serial creatinine measurements between baseline and day 3, 5 (2.9%) developed CIN. The incidence of CIN was 2% in patients who were scanned before a baseline creatinine level was available.</P>
<P><B>CONCLUSION:</B> The incidence of renal sequelae is relatively low in acute stroke patients undergoing emergent multimodal CT scanning. Prompt CTA/CTP imaging of acute stroke, if indicated, need not be delayed in those with no history of renal impairment.</P>
]]></description>
<dc:creator><![CDATA[Hopyan, J.J., Gladstone, D.J., Mallia, G., Schiff, J., Fox, A.J., Symons, S.P., Buck, B.H., Black, S.E., Aviv, R.I.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1257</dc:identifier>
<dc:title><![CDATA[[BRAIN] Renal Safety of CT Angiography and Perfusion Imaging in the Emergency Evaluation of Acute Stroke]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1830</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1826</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1831?rss=1">
<title><![CDATA[[BRAIN] CT Perfusion Quantification of Small-Vessel Ischemic Severity]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1831?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Cerebral blood flow (CBF) abnormalities are previously demonstrated in white matter disease. A gradation of change may exist between patients with mild and more severe white matter disease. An association between blood brain barrier dysfunction, increasing age and white matter disease is also suggested. The purpose of this study was to quantify and correlate white matter disease severity and CT perfusion (CTP)-derived CBF and to determine whether permeability surface abnormality increases with white matter disease severity.</P>
<P><B>MATERIALS AND METHODS:</B> One hundred twenty patients with strokelike symptoms underwent CTP and MR imaging. Of these, 35 patients (15 women, 20 men; age, 66 &plusmn; 15.7 years) with rapidly resolving symptoms and normal imaging characteristics consistent with transient ischemic attack were retrospectively reviewed and constituted the study cohort. Two blinded neurologists rated white matter severity, assigning age-related white matter change (ARWMC) scores. Patients were dichotomized a priori into mild and moderate-to-severe. CBF, cerebral blood volume (CBV), mean transit time (MTT), and permeability surface product maps were calculated for periventricular and subcortical white matter regions and average white and gray matter. Associations with white matter severity were tested by uni- and multivariate logistic regression analyses. Receiver operating characteristic analysis was performed.</P>
<P><B>RESULTS:</B> White matter disease was mild in 26 patients and moderate-to-severe in 9. Age was associated with increased likelihood of having moderate-to-severe white matter disease (<I>P</I> = .02). ARWMC correlated with subcortical (<I>r</I> = &ndash;0.50, <I>P</I> &lt; .001) and average CBF (<I>r</I> = &ndash;0.55, <I>P</I> &lt; .001). White matter severity was associated with subcortical (<I>P</I> = .03) and average (<I>P</I> = .03) white matter CBF, with a trend toward periventricular white matter CBF (<I>P</I> = .05). Uni- and multivariate analysis controlling for the confounding effect of age demonstrated significant association between white matter severity and subcortical (<I>P</I> = .032) white matter CBF. Area under the curve was 0.82. No permeability surface abnormality was found.</P>
<P><B>CONCLUSIONS:</B> CTP-derived subcortical white matter CBF is independently associated with white matter disease severity.</P>
]]></description>
<dc:creator><![CDATA[Huynh, T.J., Murphy, B., Pettersen, J.A., Tu, H., Sahlas, D.J., Zhang, L., Symons, S.P., Black, S., Lee, T.-Y., Aviv, R.I.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1238</dc:identifier>
<dc:title><![CDATA[[BRAIN] CT Perfusion Quantification of Small-Vessel Ischemic Severity]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1836</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1831</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1837?rss=1">
<title><![CDATA[[BRAIN] Use of CT Angiography for Anatomic Localization of Arteriovenous Malformation Nidal Components]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1837?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We report a case of diffuse arteriovenous malformation (AVM) in basal ganglia and an internal capsule associated with venous aneurysms. The patient was treated by embolization guided by CT angiography to target the basal ganglionic portion of the AVM while sparing the internal capsule. Our case demonstrates that it is possible to obtain good quality intranidal angiograms by using CT angiography, which can be useful for exact localization of the catheterized part of the nidus.</P>
]]></description>
<dc:creator><![CDATA[Gupta, V., Chugh, M., Walia, B.S., Vaishya, S., Jha, A.N.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1136</dc:identifier>
<dc:title><![CDATA[[BRAIN] Use of CT Angiography for Anatomic Localization of Arteriovenous Malformation Nidal Components]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1840</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1837</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1841?rss=1">
<title><![CDATA[[BRAIN] Chronic Middle Cerebral Artery Occlusion: A Hemodynamic and Metabolic Study with Positron-Emission Tomography]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1841?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Chronic middle cerebral artery (MCA) occlusion is more common than generally thought. It is important to assess the cerebral hemodynamic status in patients with this chronic condition. We investigated the cerebral hemodynamic and metabolic disturbances in these patients in relation to the development of the collateral vasculature.</P>
<P><B>MATERIALS AND METHODS:</B> We studied 13 patients with chronic unilateral MCA occlusion who had a minor or no stroke by using positron-emission tomography (PET). PET was performed by the oxygen 15 (<SUP>15</SUP>O) gas steady-state inhalation method. The intracranial arteries were evaluated by digital subtraction angiography. We divided the patients into 2 subgroups according to whether they had a normal or increased oxygen extraction fraction (OEF) in the occluded MCA territory and compared the 2 groups.</P>
<P><B>RESULTS:</B> Of the 13 patients, 9 were classified into the normal OEF and 4 were classified into the increased OEF group. In the increased OEF group, the mean OEF values were also increased in the territories of the ipsilateral anterior cerebral artery, ipsilateral posterior cerebral artery, and contralateral MCA. The patients in the increased OEF group had more than 1 steno-occlusive lesion in the major intracranial arteries (<I>P</I> = .008). Three of the 4 patients in the increased OEF group also had vascular lesions in the collateral pathways to the MCA territory.</P>
<P><B>CONCLUSION:</B> Most patients with chronic MCA occlusion did not show severe hemodynamic impairment. Those with increased OEF tended to have other areas of severe hemodynamic impairment and other vascular lesions, especially in the collateral pathways.</P>
]]></description>
<dc:creator><![CDATA[Tanaka, M., Shimosegawa, E., Kajimoto, K., Kimura, Y., Kato, H., Oku, N., Hori, M., Kitagawa, K., Hatazawa, J.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1234</dc:identifier>
<dc:title><![CDATA[[BRAIN] Chronic Middle Cerebral Artery Occlusion: A Hemodynamic and Metabolic Study with Positron-Emission Tomography]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1846</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1841</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1847?rss=1">
<title><![CDATA[[BRAIN] 3D Time-Resolved MR Angiography (MRA) of the Carotid Arteries with Time-Resolved Imaging with Stochastic Trajectories: Comparison with 3D Contrast-Enhanced Bolus-Chase MRA and 3D Time-Of-Flight MRA]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1847?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Time-resolved MR angiography (MRA) offers the combined advantage of large anatomic coverage and hemodynamic flow information. We applied parallel imaging and time-resolved imaging with stochastic trajectories (TWIST), which uses a spiral trajectory to undersample <I>k</I>-space, to perform time-resolved MRA of the extracranial internal carotid arteries and compare it to time-of-flight (TOF) and high-resolution contrast-enhanced (HR) MRA.</P>
<P><B>MATERIALS AND METHODS:</B> A retrospective review of 31 patients who underwent carotid MRA at 1.5T using TOF, time-resolved and HR MRA was performed. Images were evaluated for the presence and degree of ICA stenosis, reader confidence, and number of pure arterial frames attained with the TWIST technique.</P>
<P><B>RESULTS:</B> With a consensus interpretation of all sequences as the reference standard, accuracy for identifying stenosis was 90.3% for TWIST MRA, compared with 96.0% and 88.7% for HR MRA and TOF MRA, respectively. HR MRA was significantly more accurate than the other techniques (<I>P</I> &lt; .05). TWIST MRA yielded datasets with high in-plane spatial resolution and distinct arterial and venous phases. It provided dynamic information not otherwise available. Mean diagnostic confidence was satisfactory or greater for TWIST in all patients.</P>
<P><B>CONCLUSION:</B> The TWIST technique consistently obtained pure arterial phase images while providing dynamic information. It is rapid, uses a low dose of contrast, and may be useful in specific circumstances, such as in the acute stroke setting. However, it does not yet have spatial resolution comparable with standard contrast-enhanced MRA.</P>
]]></description>
<dc:creator><![CDATA[Lim, R.P., Shapiro, M., Wang, E.Y., Law, M., Babb, J.S., Rueff, L.E., Jacob, J.S., Kim, S., Carson, R.H., Mulholland, T.P., Laub, G., Hecht, E.M.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1252</dc:identifier>
<dc:title><![CDATA[[BRAIN] 3D Time-Resolved MR Angiography (MRA) of the Carotid Arteries with Time-Resolved Imaging with Stochastic Trajectories: Comparison with 3D Contrast-Enhanced Bolus-Chase MRA and 3D Time-Of-Flight MRA]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1854</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1847</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1855?rss=1">
<title><![CDATA[[BRAIN] Collateral Circulation Imaging: MR Perfusion Territory Arterial Spin-Labeling at 3T]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1855?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Current knowledge of the collateral circulation remains sparse, and a noninvasive method to better characterize the role of collaterals is desirable. The aim of our study was to investigate the presence and distal flow of collaterals by using a new MR perfusion territory imaging, vessel-encoded arterial spin-labeling (VE-ASL).</P>
<P><B>MATERIALS AND METHODS:</B> Fifty-six patients with internal carotid artery (ICA) or middle cerebral artery (MCA) stenosis were identified by sonography. VE-ASL was performed to assess the presence and function of collateral flow. The perfusion information was combined with VE maps into high signal-intensity-to-noise-ratio 3-colored maps of the left carotid, right carotid, and posterior circulation territories. The presence of the anterior and posterior collateral flow was demonstrated by the color of the standard anterior cerebral artery/MCA flow territory. The distal function of collateral flow was categorized as adequate (cerebral blood flow [CBF] &ge;10 mL/min/100 g) or deficient (CBF &lt;10 mL/min/100 g). The results were compared with those of MR angiography (MRA) and intra-arterial digital subtraction angiography (DSA) in cross table, and  coefficients were calculated to determine the agreement among different methods.</P>
<P><B>RESULTS:</B> The  coefficients of the presence of anterior and posterior collaterals by using VE-ASL and MRA were 0.785 and 0.700, respectively. The  coefficient of the function of collaterals by using VE-ASL and DSA was 0.726. Apart from collaterals through the circle of Willis, VE-ASL showed collateral flow via leptomeningeal anastomoses.</P>
<P><B>CONCLUSIONS:</B> In patients with ICA or MCA stenosis, VE-ASL could show the presence, the origin, and distal function of collateral flow noninvasively.</P>
]]></description>
<dc:creator><![CDATA[Wu, B., Wang, X., Guo, J., Xie, S., Wong, E.C., Zhang, J., Jiang, X., Fang, J.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1259</dc:identifier>
<dc:title><![CDATA[[BRAIN] Collateral Circulation Imaging: MR Perfusion Territory Arterial Spin-Labeling at 3T]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1860</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1855</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1861?rss=1">
<title><![CDATA[[BRAIN] Pilomyxoid Astrocytoma: Expanding the Imaging Spectrum]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1861?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Pilomyxoid astrocytoma (PMA) is a recently described variant of pilocytic astrocytoma (PA) with unique clinical and histopathologic characteristics. Because the histopathology of PMA is distinct from that of PA, we hypothesized that PMAs would display distinctive imaging characteristics. We retrospectively reviewed the imaging findings in a large number of patients with PMA to identify these characteristics.</P>
<P><B>MATERIALS AND METHODS:</B> CT and MR images, pathology reports, and clinical information from 21 patients with pathology-confirmed PMA from 7 institutions were retrospectively reviewed. CT and MR imaging findings, including location, size, signal intensity, hemorrhage, and enhancement pattern, were tabulated.</P>
<P><B>RESULTS:</B> Patients ranged in age from 9 months to 46 years at initial diagnosis. Sex ratio was 12:9 (M/F). Twelve of 21 (57%) tumors were located in the hypothalamic/chiasmatic/third ventricular region. Nine (43%) occurred in other locations, including the parietal lobe (2/21), temporal lobe (2/21), cerebellum (2/21), basal ganglia (2/21), and fourth ventricle (1/21). Ten (48%) tumors showed heterogeneous rim enhancement, 9 (43%) showed uniform enhancement, and 2 (9%) showed no enhancement. Five (24%) masses demonstrated intratumoral hemorrhage.</P>
<P><B>CONCLUSION:</B> This series expands the clinical and imaging spectrum of PMA and identifies characteristics that should suggest consideration of this uncommon diagnosis. One third of patients were older children and adults. Almost half of all tumors were located outside the typical hypothalamic/chiasmatic region. Intratumoral hemorrhage occurred in one quarter of patients. PMA remains a histologic diagnosis without definitive imaging findings that distinguish it from PA.</P>
]]></description>
<dc:creator><![CDATA[Linscott, L.L., Osborn, A.G., Blaser, S., Castillo, M., Hewlett, R.H., Wieselthaler, N., Chin, S.S., Krakenes, J., Hedlund, G.L., Sutton, C.L.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1233</dc:identifier>
<dc:title><![CDATA[[BRAIN] Pilomyxoid Astrocytoma: Expanding the Imaging Spectrum]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1866</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1861</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1867?rss=1">
<title><![CDATA[[BRAIN] Analysis of 11C-methionine Uptake in Low-Grade Gliomas and Correlation with Proliferative Activity]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1867?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> The relationship of <SUP>11</SUP>C-methionine (MET) uptake and tumor activity in low-grade gliomas (those meeting the criteria for World Health Organization [WHO] grade II gliomas) remains uncertain. The aim of this study was to compare MET uptake in low-grade gliomas and to analyze whether MET positron-emission tomography (PET) can estimate tumor viability and provide evidence of malignant transformation.</P>
<P><B>MATERIALS AND METHODS:</B> We studied glioma metabolic activity in 49 consecutive patients with newly diagnosed grade II gliomas by using MET PET before surgical resection. On MET PET, we measured tumor/normal brain uptake ratio (T/N ratio) in 21 diffuse astrocytomas (DAs), 12 oligodendrogliomas (ODs), and 16 oligoastrocytomas (OAs). We compared MET T/N ratio among these 3 tumors and investigated possible correlation with proliferative activity, as measured by Mib-1 labeling index (LI).</P>
<P><B>RESULTS:</B> MET T/N ratios of DA, OD, and OA were 2.11 &plusmn; 0.87, 3.75 &plusmn; 1.43, and 2.76 &plusmn; 1.27, respectively. The MET T/N ratio of OD was significantly higher than that of DA (<I>P</I> &lt; .005). In comparison of MET T/N ratios with the Mib-1 LI, a significant correlation was shown in DA (<I>r</I> = 0.63; <I>P</I> &lt; .005) but not in OD and OA.</P>
<P><B>CONCLUSION:</B> MET uptake in DAs may be closely associated with tumor viability, which depends on increased amino acid transport by an activated carrier-mediated system. DAs with lower MET uptake were considered more quiescent lesions, whereas DA with higher MET uptake may act more aggressively.</P>
]]></description>
<dc:creator><![CDATA[Kato, T., Shinoda, J., Oka, N., Miwa, K., Nakayama, N., Yano, H., Maruyama, T., Muragaki, Y., Iwama, T.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1242</dc:identifier>
<dc:title><![CDATA[[BRAIN] Analysis of 11C-methionine Uptake in Low-Grade Gliomas and Correlation with Proliferative Activity]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1871</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1867</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1872?rss=1">
<title><![CDATA[[BRAIN] Preoperative Grading of Presumptive Low-Grade Astrocytomas on MR Imaging: Diagnostic Value of Minimum Apparent Diffusion Coefficient]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1872?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Histopathologic grade of glial tumors is inversely correlated with the minimum apparent diffusion coefficient (ADC). We assessed the diagnostic values of minimum ADC for preoperative grading of supratentorial astrocytomas that were diagnosed as low-grade astrocytomas on conventional MR imaging.</P>
<P><B>MATERIALS AND METHODS:</B> Among 118 patients with astrocytomas (WHO grades II&ndash;IV), 16 who showed typical MR imaging findings of low-grade supratentorial astrocytomas on conventional MR imaging were included. All 16 patients underwent preoperative MR imaging and diffusion-weighted imaging. The minimum ADC value of each tumor was determined from several regions of interest in the tumor on ADC maps. To assess the relationship between the minimum ADC and tumor grade, we performed the Mann-Whitney <I>U</I> test. A receiver operating characteristic (ROC) analysis was used to determine the cutoff value of the minimum ADC that had the best combination of sensitivity and specificity for distinguishing low- and high-grade astrocytomas.</P>
<P><B>RESULTS:</B> Eight of the 16 patients (50%) were confirmed as having high-grade astrocytomas (WHO grades III and IV), and the other 8 patients were confirmed as having low-grade astrocytomas (WHO grade II). The median minimum ADC of the high-grade astrocytoma (1.035 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP> &middot; sec<SUP>&ndash;1</SUP>) group was significantly lower than that of the low-grade astrocytoma group (1.19 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP> &middot; sec<SUP>&ndash;1</SUP>) (<I>P</I> = .021). According to the ROC analysis, the cutoff value of 1.055 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP> &middot; sec<SUP>&ndash;1</SUP> for the minimum ADC generated the best combination of sensitivity (87.5%) and specificity (79%) (<I>P</I> = .021).</P>
<P><B>CONCLUSION:</B> Measuring minimum ADC can provide valuable diagnostic information for the preoperative grading of presumptive low-grade supratentorial astrocytomas.</P>
]]></description>
<dc:creator><![CDATA[Lee, E.J., Lee, S.K., Agid, R., Bae, J.M., Keller, A., terBrugge, K.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1254</dc:identifier>
<dc:title><![CDATA[[BRAIN] Preoperative Grading of Presumptive Low-Grade Astrocytomas on MR Imaging: Diagnostic Value of Minimum Apparent Diffusion Coefficient]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1877</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1872</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1878?rss=1">
<title><![CDATA[[BRAIN] Primary Sjogren Syndrome with Tumefactive Central Nervous System Involvement]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1878?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Brain MR imaging abnormalities in primary Sj&ouml;gren syndrome (pSS) are generally discrete white matter lesions. We describe a 50-year-old woman with recurrent neurologic deficits. MR imaging revealed a large brain lesion. A diagnosis of pSS was made on the basis of clinical features, positive anti-Ro and anti-La antibodies, abnormal Schirmer test findings, and salivary gland scintigraphy. The patient was treated with oral prednisone with good response. Large tumefactive brain lesions are a complication of pSS.</P>
]]></description>
<dc:creator><![CDATA[Sanahuja, J., Ordonez-Palau, S., Begue, R., Brieva, L., Boquet, D.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1204</dc:identifier>
<dc:title><![CDATA[[BRAIN] Primary Sjogren Syndrome with Tumefactive Central Nervous System Involvement]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1879</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1878</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1880?rss=1">
<title><![CDATA[[BRAIN] CT and MR Imaging of Progressive Dural Involvement by Nephrogenic Systemic Fibrosis]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1880?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We present a patient with progressive dural calcifications, thickening, and enhancement presumably related to the development of nephrogenic systemic fibrosis (NSF). Head CT demonstrated progressive dural calcifications, whereas MR imaging demonstrated progressive dural thickening and enhancement during a 3-year period in which the patient received several gadolinium-enhanced MR imaging studies. To the best of our knowledge, dural calcifications are the only described intracranial finding of NSF.</P>
]]></description>
<dc:creator><![CDATA[Zelasko, S., Hollingshead, M., Castillo, M., Bouldin, T.W.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1225</dc:identifier>
<dc:title><![CDATA[[BRAIN] CT and MR Imaging of Progressive Dural Involvement by Nephrogenic Systemic Fibrosis]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1882</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1880</prism:startingPage>
<prism:section>BRAIN</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1883?rss=1">
<title><![CDATA[[FUNCTIONAL] Functional Connectivity MR Imaging Reveals Cortical Functional Connectivity in the Developing Brain]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1883?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Unlike conventional functional MR imaging where external sensory/cognitive paradigms are needed to specifically activate different regions of the brain, resting functional connectivity MR imaging acquires images in the absence of cognitive demands (a resting condition) and detects brain regions, which are highly temporally correlated. Therefore, resting functional MR imaging is highly suited for the study of brain functional development in pediatric subjects. This study aimed to determine the temporal and spatial patterns of rfc in healthy pediatric subjects between 2 weeks and 2 years of age.</P>
<P><B>MATERIALS AND METHODS:</B> Rfc studies were performed on 85 children: 38 neonates (2&ndash;4 weeks of age), 26 one-year-olds, and 21 two-year-olds. All subjects were imaged while asleep; no sedation was used. Six regions of interest were chosen, including the primary motor, sensory, and visual cortices in each hemisphere. Mean signal intensity of each region of interest was used to perform correlation analysis pixel by pixel throughout the entire brain, identifying regions with high temporal correlation.</P>
<P><B>RESULTS:</B> Functional connectivity was observed in all subjects in the sensorimotor and visual areas. The percent brain volume exhibiting rfc and the strength of rfc continued to increase from 2 weeks to 2 years. The growth trajectories of the percent brain volume of rfc appeared to differ between the sensorimotor and visual areas, whereas the <I>z</I>-score was similar. The percent brain volume of rfc in the sensorimotor area was significantly larger than that in the visual area for subjects 2 weeks of age (<I>P</I> = .008) and 1-year-olds (<I>P</I> = .017) but not for the 2-year-olds.</P>
<P><B>CONCLUSIONS:</B> These findings suggest that rfc in the sensorimotor precedes that in the visual area from 2 weeks to 1 year but becomes comparable at 2 years. In contrast, the comparable <I>z</I>-score values between the sensorimotor and visual areas for all age groups suggest a disassociation between percent brain volume and the strength of cortical rfc.</P>
]]></description>
<dc:creator><![CDATA[Lin, W., Zhu, Q., Gao, W., Chen, Y., Toh, C.-H., Styner, M., Gerig, G., Smith, J.K., Biswal, B., Gilmore, J.H.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1256</dc:identifier>
<dc:title><![CDATA[[FUNCTIONAL] Functional Connectivity MR Imaging Reveals Cortical Functional Connectivity in the Developing Brain]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1889</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1883</prism:startingPage>
<prism:section>FUNCTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1890?rss=1">
<title><![CDATA[[FUNCTIONAL] Patterns of Brain Activation during Visually Evoked Sexual Arousal Differ between Homosexual and Heterosexual Men]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1890?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Nowadays the mechanism of homosexuality is little known. Few studies have been carried out to explore the brain functional changes of homosexual men during sexual arousal. We used functional MR imaging (fMRI) to determine whether the patterns of brain activation in homosexual and heterosexual men differed during visually evoked sexual arousal.</P>
<P><B>MATERIALS AND METHODS:</B> To all the subjects (10 homosexual and 10 heterosexual), real-time visual stimulation was provided by 3-minute exposure to 3 types of erotic film: heterosexual couples (F-M), male homosexual couples (M-M), and female homosexual couples (F-F) engaged in sexual activity, during which time fMRI was used to determine the patterns of brain activation. Self-reports of level of sexual arousal were collected immediately afterward.</P>
<P><B>RESULTS:</B> Statistical parametric mapping showed that viewing erotic film excerpts that induced sexual arousal was associated, in both groups, with activation of the middle prefrontal gyrus, bilateral temporal lobe and postcentral gyrus, thalamus, insula, vermis, left precuneus, occipital cortex, parietal cortex, and cerebellum. In homosexual men, the left angular gyrus, left caudate nucleus, and right pallidum were activated; in contrast, heterosexual men showed no activation in these regions. However, heterosexual men showed activation in the bilateral lingual gyrus, right hippocampus, and right parahippocampal gyrus, areas not activated in homosexual men. In both groups, region-of-interest analysis revealed no correlation between the magnitude of amygdala or thalamus activation and the reported level of sexual arousal.</P>
<P><B>CONCLUSION:</B> Our findings indicate that different neural circuits are active during sexual arousal in homosexual and heterosexual men and may contribute to a better understanding of the neural basis of male sexual orientation.</P>
]]></description>
<dc:creator><![CDATA[Hu, S.-h., Wei, N., Wang, Q.-D., Yan, L.-q., Wei, E.-Q., Zhang, M.-M., Hu, J.-B., Huang, M.-l., Zhou, W.-h., Xu, Y.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1260</dc:identifier>
<dc:title><![CDATA[[FUNCTIONAL] Patterns of Brain Activation during Visually Evoked Sexual Arousal Differ between Homosexual and Heterosexual Men]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1896</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1890</prism:startingPage>
<prism:section>FUNCTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1897?rss=1">
<title><![CDATA[[HEAD & NECK] Diffusion-Weighted MR Imaging of Ameloblastomas and Keratocystic Odontogenic Tumors: Differentiation by Apparent Diffusion Coefficients of Cystic Lesions]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1897?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Ameloblastomas and keratocystic odontogenic tumors are major aggressive odontogenic tumors in the maxillomandibular regions, but the differentiation between these 2 tumors is frequently ineffective based on only conventional CT and MR imaging findings. Here, we evaluated diffusion-weighted MR imaging for the differentiation of these 2 odontogenic tumors.</P>
<P><B>MATERIALS AND METHODS:</B> We prospectively studied 9 patients with ameloblastoma and 7 patients with keratocystic odontogenic tumor using diffusion-weighted MR imaging. Apparent diffusion coefficients (ADCs) of the nonenhancing and solid lesions in these tumors were determined with use of 2 b factors (500 and 1000).</P>
<P><B>RESULTS:</B> Two types of nonenhancing lesions were identified; one with high signal intensity on fat-suppressed T2-weighted images (type A) and the other with low or intermediate intensity (type B). The type A nonenhancing lesions were observed in all the ameloblastomas, but they were evident in only 2 keratocystic odontogenic tumors. It is interesting to note that the ADCs of the nonenhancing lesions in the ameloblastomas were significantly higher than those of the nonenhancing lesions in the keratocystic odontogenic tumors (2.48 &plusmn; 0.20 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP>/s vs 1.13 &plusmn; 0.56 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP>/s; <I>P</I> &lt; .001). The ADCs of the solid lesions in the ameloblastomas (1.39 &plusmn; 0.15 <FONT FACE="arial,helvetica">x</FONT> 10<SUP>&ndash;3</SUP> mm<SUP>2</SUP>/s) were significantly lower than those of the nonenhancing lesions in the ameloblastomas and were similar to those of the nonenhancing lesions in the keratocystic odontogenic tumors.</P>
<P><B>CONCLUSION:</B> ADC determination may be used as an adjunct tool for differentiation between ameloblastomas and keratocystic odontogenic tumors.</P>
]]></description>
<dc:creator><![CDATA[Sumi, M., Ichikawa, Y., Katayama, I., Tashiro, S., Nakamura, T.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1266</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] Diffusion-Weighted MR Imaging of Ameloblastomas and Keratocystic Odontogenic Tumors: Differentiation by Apparent Diffusion Coefficients of Cystic Lesions]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1901</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1897</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1902?rss=1">
<title><![CDATA[[HEAD & NECK] Whole-Body CT Trauma Imaging with Adapted and Optimized CT Angiography of the Craniocervical Vessels: Do We Need an Extra Screening Examination?]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1902?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Blunt carotid and vertebral artery injury (BCVI) is rare but potentially devastating. The objective of our study was to prospectively evaluate the usefulness of a dedicated and optimized CT angiography (CTA) protocol of the craniocervical vessels as part of a whole-body CT work-up of patients with multiple trauma in a population of patients with blunt trauma.</P>
<P><B>MATERIAL AND METHODS:</B> From February 2006 to July 2007, a total of 368 consecutive patients with trauma were evaluated. All examinations were performed on a 16-row multisection CT (MSCT) scanner. CTA was performed from the level of the T2 vertebra to the roof of the lateral ventricles with 40 mL of iodinated contrast agent. Images were reconstructed with use of the angiography and bone window settings to evaluate vessels and bones.</P>
<P><B>RESULTS:</B> Of all eligible patients imaged, 100 had injuries to the head and neck including 35 skull base fractures (9.5%), 24 maxillofacial (6.5%), and 11 cervical spine fractures (3%). CTA was diagnostic in all patients. BCVI was diagnosed in 6 cases (6 lesions of the internal carotid artery, 3 lesions of the vertebral artery); among them were 2 who did not meet the screening criteria. No patient with negative results on CTA subsequently had development of neurologic deficits suspicious for BCVI.</P>
<P><B>CONCLUSION:</B> This study confirms that optimized craniocervical CTA can be easily integrated into a whole-body CT protocol for patients with multiple trauma. No additional screening technique is necessary to identify clinically relevant vascular injuries. Earlier recognition enables earlier treatment and may decrease mortality and morbidity rates of these rare but potentially devastating injuries.</P>
]]></description>
<dc:creator><![CDATA[Langner, S., Fleck, S., Kirsch, M., Petrik, M., Hosten, N.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1261</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] Whole-Body CT Trauma Imaging with Adapted and Optimized CT Angiography of the Craniocervical Vessels: Do We Need an Extra Screening Examination?]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1907</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1902</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1908?rss=1">
<title><![CDATA[[HEAD & NECK] Diffuse Lipogranulomatosis Involving Soft Tissues of the Head and Neck due to Multiple Self-Injections of Mineral Oil]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1908?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We describe imaging findings of a 45-year-old man with a 6-month history of gradually increasing diffuse swelling of the neck. CT showed diffuse thickening and infiltration of the superficial and deep soft tissues bilaterally. On further investigation of his history, the patient stated that he had injected mineral oil into his neck to clean out his body from drugs. Biopsy results showed multinucleated giant cells and inflammatory infiltrates confirming the diagnosis of lipogranulomatosis.</P>
]]></description>
<dc:creator><![CDATA[Kathuria, S., Westesson, P.-L.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1192</dc:identifier>
<dc:title><![CDATA[[HEAD & NECK] Diffuse Lipogranulomatosis Involving Soft Tissues of the Head and Neck due to Multiple Self-Injections of Mineral Oil]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1909</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1908</prism:startingPage>
<prism:section>HEAD &amp; NECK</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1910?rss=1">
<title><![CDATA[[INTERVENTIONAL] Dose Measurement on Both Patients and Operators during Neurointerventional Procedures Using Photoluminescence Glass Dosimeters]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1910?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Although radiation skin injuries associated with interventional radiology have been known as a critical issue, there are few reports mentioning direct measurement of the entrance skin dose (ESD). Thus, the purpose of this study was to clarify the regional distributions of ESDs in neurointervention.</P>
<P><B>MATERIALS AND METHODS:</B> Using photoluminescence glass dosimeters (PLDs), we measured the ESDs in 32 patients with a median age of 61.5 years. Angiographic parameters, including exposure time, dose-area product (DAP), and the number of digital subtraction angiography (DSA) studies and frames, were recorded. The ESDs of operators were analyzed by the same method.</P>
<P><B>RESULTS:</B> The maximum ESD of 28 therapeutic procedures was 1.8 &plusmn; 1.3 Gy. Although the averaged ESD on the right temporo-occipital region was higher than that in other regions, disease-specific patterns were not observed. Statistically positive correlations were found between the maximum ESD and exposure time (<I>r</I> = 0.5283, <I>P</I> = .005), DAP (<I>r</I> = 0.7917, <I>P</I> &lt; .001), the number of DSA studies (<I>r</I> = 0.5636, <I>P</I> = .002), and the number of DSA frames (<I>r</I> = 0.8583, <I>P</I> &lt; .001). As for operators, ESDs to the left upper extremity were significantly higher than those to other regions. However, most of the ESDs were &lt;0.2 mGy. Lead protective garments reduced the exposure doses to approximately one half to one tenth.</P>
<P><B>CONCLUSION:</B> It was shown that the regional ESD could be measured by applying the PLD. This method should contribute to reducing the dose accumulation in patients as well as in operators.</P>
]]></description>
<dc:creator><![CDATA[Moritake, T., Matsumaru, Y., Takigawa, T., Nishizawa, K., Matsumura, A., Tsuboi, K.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1235</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Dose Measurement on Both Patients and Operators during Neurointerventional Procedures Using Photoluminescence Glass Dosimeters]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1917</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1910</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1918?rss=1">
<title><![CDATA[[INTERVENTIONAL] Endovascular Interventions following Intravenous Thrombolysis May Improve Survival and Recovery in Patients with Acute Ischemic Stroke: A Case-Control Study]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1918?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Since the introduction of recombinant tissue plasminogen activator (rtPA) into clinical practice in the mid 1990s, no adjunctive treatment has further improved clinical outcomes in patients with ischemic stroke. The safety, feasibility, and efficacy of combining intravenous (IV) rtPA with endovascular interventions has been described; however, no direct comparative study has yet established whether endovascular interventions after IV rtPA are superior to IV rtPA alone. A retrospective case-control study was designed to address this issue.</P>
<P><B>MATERIALS AND METHODS:</B> Between 2003 and 2006, 33 consecutive patients with acute ischemic stroke and National Institutes of Health Stroke Scale (NIHSS) scores &ge;10 were treated with IV rtPA in combination with endovascular interventions (IV plus intervention) at a tertiary care facility. Outcomes were compared with a control cohort of 30 consecutive patients treated with IV rtPA (IV only) at a comparable facility where endovascular interventions were not available.</P>
<P><B>RESULTS:</B> Baseline parameters were similar between the 2 groups. We found that the IV-plus-intervention group experienced significantly lower mortality at 90 days (12.1% versus 40.0%, <I>P</I> = .019) with a significantly greater improvement in NIHSS scores by the time of discharge or follow-up (<I>P</I> = .025). In the IV-plus-intervention group, patients with admission NIHSS scores between 10 and 15 and patients &le;80 years of age showed the greatest improvement, with a significant change of the NIHSS scores from admission (<I>P</I> = .00015 and <I>P</I> = .013, respectively).</P>
<P><B>CONCLUSIONS:</B> In this small case-control study of patients with acute ischemic stroke and admission NIHSS scores &ge;10, there was a suggestion of incremental clinical benefit among patients receiving endovascular interventions following standard administration of IV rtPA.</P>
]]></description>
<dc:creator><![CDATA[Burns, T.C., Rodriguez, G.J., Patel, S., Hussein, H.M., Georgiadis, A.L., Lakshminarayan, K., Qureshi, A.I.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1236</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Endovascular Interventions following Intravenous Thrombolysis May Improve Survival and Recovery in Patients with Acute Ischemic Stroke: A Case-Control Study]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1924</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1918</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1925?rss=1">
<title><![CDATA[[INTERVENTIONAL] Abciximab for Treatment of Thromboembolic Complications during Endovascular Coiling of Intracranial Aneurysms]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1925?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Thromboembolism is a recognized complication occurring during endovascular coil embolization of intracranial aneurysms. Recently, there has been much interest in glycoprotein IIb/IIIa inhibitors to treat such complications, but the evidence is limited. We reviewed our use of one such agent, abciximab, which we commonly administer and believe to be a safe and suitable rescue agent in this setting.</P>
<P><B>MATERIALS AND METHODS:</B> We retrospectively reviewed cases in which abciximab was administered in our institution between 2001 and 2007. Clinical outcome was assessed by the modified Rankin Scale (mRS) at 6 months. Good outcome was defined as no significant clinical sequelae compared with baseline status or clinical improvement (mRS &lt; 2). Poor outcome was defined as no resolution of a new clinical deficit that developed postprocedure at 6 months (mRS &gt; 2). Angiographic appearance of thromboembolic phenomena and posttreatment outcome was assessed with the Thrombolysis in Myocardial Infarction (TIMI) scale.</P>
<P><B>RESULTS:</B> Thirty-eight patients were included, with good outcome observed in 30 (79%) and poor outcome in 8 (21%) patients. Angiographic improvement based on TIMI scoring was seen in 24 (63%) patients, and no improvement was seen in 14 (37%). In 4 patients (11%), good outcome was obtained at 6 months despite no angiographic improvement on TIMI. No cases of intracranial rebleed or additional neurologic deficit following administration of abciximab were encountered.</P>
<P><B>CONCLUSION:</B> In this small retrospective series, abciximab was safe and effective when used as a rescue agent for thromboembolic complications encountered during coiling of intracerebral aneurysms.</P>
]]></description>
<dc:creator><![CDATA[Jones, R.G., Davagnanam, I., Colley, S., West, R.J., Yates, D.A.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1253</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Abciximab for Treatment of Thromboembolic Complications during Endovascular Coiling of Intracranial Aneurysms]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1929</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1925</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1930?rss=1">
<title><![CDATA[[INTERVENTIONAL] Neuroradiologic Applications with Routine C-arm Flat Panel Detector CT: Evaluation of Patient Dose Measurements]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1930?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Since the introduction of flat panel detector&ndash;equipped C-arms, the use of flat panel detector CT (FPCT) in the neuroradiologic angiography suite has become more frequent. This examination implicates its own specific radiation exposure. We used the CT dose index (CTDI) concept and adapted it to the special FPCT geometry to provide a consistent comparison with multisection head CT (cCT).</P>
<P><B>MATERIALS AND METHODS:</B> Exposure data obtained for routine scanning during a period of 1 year were used to assess a specific dose of a total of 217 rotational scans performed in 105 patients. One hundred seventy-two scans were 3D digital subtraction angiography (DSA) scans. There were 45 scans that were performed to achieve high-quality, soft-tissue resolution. Dose measurements in cylindrical polymethylmethacrylate (PMMA) phantoms were used to determine the CTDI value and to compare it with the reference values for cCT. In addition, the dose-area product (DAP) was registered and correlated with the CTDI and corresponding dose-length product (DLP) values. Exposure data and dose values were compared with cCT.</P>
<P><B>RESULTS:</B> Mean-weighted CTDI value of 3D-DSA was approximately 9 mGy per scan. High-quality, soft-tissue resolution FPCT scans, comparable with cCT, revealed a mean dose value of 75 mGy (reference value for cCT, CTDI<SUB>w</SUB> ~ 60 mGy).</P>
<P><B>CONCLUSION:</B> The high-speed scans used for 3D-DSA revealed a significantly lower CTDI<SUB>w</SUB> and DLP compared with clinical CT. The high-quality FPCT protocol resulted in a higher dose and should therefore be limited to acute cases, when patient transfer to a CT scanner is considered to be a disadvantage for patient management.</P>
]]></description>
<dc:creator><![CDATA[Kyriakou, Y., Richter, G., Dorfler, A., Kalender, W.A.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1237</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Neuroradiologic Applications with Routine C-arm Flat Panel Detector CT: Evaluation of Patient Dose Measurements]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1936</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1930</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1937?rss=1">
<title><![CDATA[[INTERVENTIONAL] Management and Clinical Outcome of Acute Basilar Artery Dissection]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1937?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> There have been inconsistencies on the prognosis and controversies as to the proper management of acute basilar artery dissection. The aim of this study was to evaluate acute basilar artery dissection and its outcome after management.</P>
<P><B>MATERIALS AND METHODS:</B> A total of 21 patients (mean age, 53 years; range, 24&ndash;78 years) with acute basilar artery dissection were identified between January 2001 and October 2007. Clinical presentation, management, and outcomes were retrospectively evaluated.</P>
<P><B>RESULTS:</B> The patients presented with subarachnoid hemorrhage (<I>n</I> = 10), brain stem ischemia (<I>n</I> = 10), or stem compression sign (<I>n</I> = 1). Ruptured basilar artery dissections were treated by stent placement with coiling (<I>n</I> = 4), single stent placement (<I>n</I> = 3), or conservatively (<I>n</I> = 3). Of the patients treated with endovascular technique, 6 had favorable outcome (modified Rankin scale [mRS], 0&ndash;2) and the remaining patient, who was treated by single stent placement, died from rebleeding. All 3 conservatively managed patients experienced rebleeding, of whom 2 died and the other was moderately disabled. Unruptured basilar artery dissections were treated conservatively (<I>n</I> = 7) or by stent placement (<I>n</I> = 4). Of the patients with unruptured basilar artery dissection, 9 had favorable outcome and the remaining 2 patients, both of whom were conservatively managed, had poor outcome because of infarct progression. The group with the ruptured basilar artery dissection revealed a higher mortality rate than the group with the unruptured dissection (30% vs 0%). The group treated with endovascular means revealed more favorable outcome than the group that was treated with conservative measures (90.9% vs 50%).</P>
<P><B>CONCLUSION:</B> The ruptured basilar artery dissections were at high risk for rebleeding, resulting in a grave outcome. Stent placement with or without coiling may be considered to prevent rebleeding in ruptured basilar dissections and judiciously considered in unruptured dissections with signs of progressive brain stem ischemia.</P>
]]></description>
<dc:creator><![CDATA[Kim, B.M., Suh, S.H., Park, S.I., Shin, Y.S., Chung, E.C., Lee, M.H., Kim, E.J., Koh, J.S., Kang, H.-s., Roh, H.G., Won, Y.S., Chung, P.-W., Kim, Y.-B., Suh, B.C.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1243</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Management and Clinical Outcome of Acute Basilar Artery Dissection]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1941</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1937</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1942?rss=1">
<title><![CDATA[[INTERVENTIONAL] Predictors and Timing of Hypotension and Bradycardia after Carotid Artery Stenting]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1942?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Hypotension and bradycardia are common in carotid artery stenting (CAS) and are particularly worrisome in the high risk patient who is typically referred for CAS. The purpose of this work was to assess the incidence and predictors of hypotension and bradycardia and the risk of their delayed occurrence after CAS.</P>
<P><B>MATERIALS AND METHODS:</B> A total of 53 men and 40 women (median age, 71 years) with symptomatic (57%) or asymptomatic (42%) carotid artery stenosis had CAS performed in our institution between December 2002 and January 2007. Patient vital sign records for the 12 hours post-CAS were analyzed. The relative decrease of blood pressure and pulse rate were used as primary end points, and the requirement of pressor or anticholinergic drugs was used as a surrogate end point. Significant predictors of hypotension and bradycardia were analyzed with a logistic regression model. Cumulative freedom from hypotension and bradycardia was calculated by using the Kaplan-Meier method. Negative predictive value (NPV) of screening for early hypotension and bradycardia was determined.</P>
<P><B>RESULTS:</B> The incidence of hypotension, bradycardia, and both was 14%, 23%, and 15%, respectively. Drug intervention was required in 45 patients (48%). Asymptomatic stenosis was an independent predictor of hypotension and bradycardia. Stenosis proximity to the bifurcation and dilation percentage were independent predictors of the drug intervention requirement. Seven patients (8%) had new onset of hypotension or bradycardia later than 6 hours post-CAS. The NPV of early hypotension and bradycardia was 97% and 93%, respectively.</P>
<P><B>CONCLUSION:</B> In this retrospective study, the risk of hypotension or bradycardia after CAS is significantly influenced by the degree of dilation performed, and the risk of their delayed occurrence may justify a minimum of 12 hours postprocedural vital sign monitoring.</P>
]]></description>
<dc:creator><![CDATA[Lavoie, P., Rutledge, J., Dawoud, M.A., Mazumdar, M., Riina, H., Gobin, Y.P.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1258</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Predictors and Timing of Hypotension and Bradycardia after Carotid Artery Stenting]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1947</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1942</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1948?rss=1">
<title><![CDATA[[INTERVENTIONAL] Successful Staged Endovascular Treatment of a Symptomatic Cervical Carotid Bifurcation Stenosis Coupled with a Coincidental Unruptured Cerebral Aneurysm in the Carotid Distal Segment]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1948?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> A 69-year-old woman had a symptomatic cervical carotid stenosis coupled with a coincidental unruptured cerebral aneurysm in the carotid distal segment. She underwent endovascular coiling for the aneurysm and then carotid stent placement (CAS) 1 month later. Both lesions were treated successfully and neither complications nor strokes occurred after the procedures. Staged endovascular treatment of coiling and subsequent CAS may be safe for patients with a cervical carotid stenosis coupled with cerebral aneurysms.</P>
]]></description>
<dc:creator><![CDATA[Iwata, T., Mori, T., Tajiri, H.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1172</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Successful Staged Endovascular Treatment of a Symptomatic Cervical Carotid Bifurcation Stenosis Coupled with a Coincidental Unruptured Cerebral Aneurysm in the Carotid Distal Segment]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1950</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1948</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1951?rss=1">
<title><![CDATA[[INTERVENTIONAL] Stent Management of Coil Herniation in Embolization of Internal Carotid Aneurysms]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1951?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Coil herniation into the parent artery after detachment is an uncommon complication of embolization of the intracranial aneurysm. We report our experience with stent reconstruction of the lumen and flow of the internal carotid artery (ICA) after coil herniation during embolization for intracranial ICA aneurysms and the possible mechanisms of coil herniation.</P>
<P><B>MATERIALS AND METHODS:</B> A series of 216 consecutive patients was treated by endovascular coil embolizations for intracranial aneurysms. Of these patients, there were 9 (4 men, 5 women; 32&ndash;68 years of age) complicating with coil herniation into the ICA and undergoing stent deployment to reconstruct the ICA lumen (<I>n</I> = 8) or both lumen and flow (<I>n</I> = 1). Wide-neck aneurysms were found in 8 and narrow-neck, in 1. Aneurysms were in the posterior communicating artery (<I>n</I> = 5) and the paraophthalmic (<I>n</I> = 3) and cavernous portions (<I>n</I> = 1) of the ICA. Self-expandable stents were deployed in the ICA in 6; balloon-mounted stents were selected in 3.</P>
<P><B>RESULTS:</B> The causes of coil herniation appeared to be coil instability after detachment (<I>n</I> = 6), excessive embolization (<I>n</I> = 1), microcatheter-related problems (<I>n</I> = 1), or being pushed by subsequent coil embolization (<I>n</I> = 1). Endovascular stent placement to reconstruct the lumen and/or flow of the ICA was technically successful in all 9 patients; 1 needed a second stent due to further coil migration. No significant procedure-related complications were found. Clinical follow-up was 8&ndash;35 months.</P>
<P><B>CONCLUSION:</B> Coil herniation occasionally occurs during endovascular embolization of ICA aneurysms because of coil instability after detachment, excessive embolization, microcatheter-related problems, or pushing by subsequent coil embolization. In this small series, stent placement was safe and effective in the reconstruction of the arterial lumen and/or restoration of flow past a herniated coil mass.</P>
]]></description>
<dc:creator><![CDATA[Luo, C.-B., Chang, F.-C., Teng, M.M.-H., Guo, W.-Y., Chang, C.-Y.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1268</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Stent Management of Coil Herniation in Embolization of Internal Carotid Aneurysms]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1955</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1951</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1956?rss=1">
<title><![CDATA[[INTERVENTIONAL] Navigability Trumps All: Stenting of Acute Middle Cerebral Artery Occlusions with a New Self-Expandable Stent]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1956?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Acute stroke intervention is rapidly evolving. New technologies are improving device deliverability and rates of recanalization. We describe 2 cases of acute middle cerebral artery occlusions wherein Wingspan stents could not be delivered to the occlusive site because of excessive vascular tortuosity. Merci thrombectomy was also unsuccessful. Revascularization was only achieved with deployment of the highly navigable Enterprise stent, resulting in thrombolysis in myocardial infarction 2/3 flow. Thus, all devices should be considered in the armamentarium of stroke therapy.</P>
]]></description>
<dc:creator><![CDATA[Chiam, P.T.L., Samuelson, R.M., Mocco, J., Hanel, R.A., Siddiqui, A.H., Hopkins, L.N., Levy, E.I.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1221</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Navigability Trumps All: Stenting of Acute Middle Cerebral Artery Occlusions with a New Self-Expandable Stent]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1958</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1956</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1959?rss=1">
<title><![CDATA[[INTERVENTIONAL] Delayed Migration of a Self-Expanding Intracranial Microstent]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1959?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> A 43-year-old patient with a basilar apex aneurysm had a 4.5-mm <FONT FACE="arial,helvetica">x</FONT> 14-mm Enterprise stent placed from the midbasilar artery to the left P1 segment of the posterior cerebral artery. The patient experienced vertigo 4 months after stent placement and 1 week after stopping clopidogrel. At 5 months postembolization, angiography showed stent migration into the proximal basilar artery. This is the first described case of the spontaneous delayed migration of a self-expanding intracranial microstent.</P>
]]></description>
<dc:creator><![CDATA[Kelly, M.E., Turner, R.D., Moskowitz, S.I., Gonugunta, V., Hussain, M.S., Fiorella, D.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1224</dc:identifier>
<dc:title><![CDATA[[INTERVENTIONAL] Delayed Migration of a Self-Expanding Intracranial Microstent]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1960</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1959</prism:startingPage>
<prism:section>INTERVENTIONAL</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1961?rss=1">
<title><![CDATA[[PEDIATRICS] Frequency and Topographic Distribution of Brain Lesions in Pediatric Cerebral Venous Thrombosis]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1961?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Cerebral sinovenous thrombosis (CSVT) is increasingly encountered in children, including neonates. The purpose of this study was to assess the frequency and topographic distribution of parenchymal brain lesions associated with CSVT in children and to compare these with the known anatomic venous drainage pathways.</P>
<P><B>MATERIALS AND METHODS:</B> Brain CT/CT venograms and/or MR imaging/MR venograms of 71 consecutive patients with CSVT were reviewed retrospectively. The patients were grouped into neonates, infants, and older children. The site of CSVT, the location and size of the brain lesions, and the presence of hemorrhage were documented. The frequency of the brain lesions was calculated.</P>
<P><B>RESULTS:</B> There were 34 neonates, 10 infants, and 27 older children with CSVT who were included. The most common sites of CSVT were the transverse sinuses, the superior sagittal sinus, and the straight sinus. Overall, 37 of 71 children with CSVT had parenchymal brain lesions. There were 21 of 34 neonates, 4 of 10 infants, and 12 of 27 older children who had brain lesions. The most common locations were in the frontal and parietal lobes. The topographic distribution of lesions correlated with the corresponding venous drainage territory in 16 of 21 neonates, all infants, and all older children. The neonates had smaller-sized lesions. Brain lesions were hemorrhagic in 76% of neonates, 75% of infants, and 33% of older children.</P>
<P><B>CONCLUSION:</B> The topographic distribution of brain lesions associated with CSVT correlates with the known drainage territories of the dural venous sinus in children.</P>
]]></description>
<dc:creator><![CDATA[Teksam, M., Moharir, M., deVeber, G., Shroff, M.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1246</dc:identifier>
<dc:title><![CDATA[[PEDIATRICS] Frequency and Topographic Distribution of Brain Lesions in Pediatric Cerebral Venous Thrombosis]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1965</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1961</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1966?rss=1">
<title><![CDATA[[PEDIATRICS] High b-Value Diffusion Tensor Imaging of the Neonatal Brain at 3T]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1966?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Diffusion-weighted MR imaging studies of the adult brain have shown that contrast between lesions and normal tissue is increased at high b-values. We designed a prospective study to test the hypothesis that diffusion tensor imaging (DTI) obtained at high b-values increases image contrast and lesion conspicuity in the neonatal brain.</P>
<P><B>MATERIALS AND METHODS:</B> We studied 17 neonates, median (range) age of 10 (2&ndash;96) days, who were undergoing MR imaging for clinical indications. DTI was performed on a Philips 3T Intera system with b-values of 350, 700, 1500, and 3000 s/mm<SUP>2</SUP>. Image contrast and lesion conspicuity at each b-value were visually assessed. In addition, regions of interest were positioned in the central white matter at the level of the centrum semiovale, frontal and occipital white matter, splenium of the corpus callosum, posterior limb of the internal capsule, and the thalamus. Apparent diffusion coefficient (ADC) and fractional anisotropy (FA) values for these regions were calculated.</P>
<P><B>RESULTS:</B> Isotropic diffusion image contrast and lesion-to-normal-tissue contrast increased with increasing b-value. ADC values decreased with increasing b-value in all regions studied; however, there was no change in FA with increasing b-value.</P>
<P><B>CONCLUSIONS:</B> Diffusion image contrast increased at high b-values may be useful in identifying lesions in the neonatal brain.</P>
]]></description>
<dc:creator><![CDATA[Dudink, J., Larkman, D.J., Kapellou, O., Boardman, J.P., Allsop, J.M., Cowan, F.M., Hajnal, J.V., Edwards, A.D., Rutherford, M.A., Counsell, S.J.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1241</dc:identifier>
<dc:title><![CDATA[[PEDIATRICS] High b-Value Diffusion Tensor Imaging of the Neonatal Brain at 3T]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1972</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1966</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1973?rss=1">
<title><![CDATA[[PEDIATRICS] Neonatal Alexander Disease: MR Imaging Prenatal Diagnosis]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1973?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Alexander disease (AD) is a rare neurodegenerative disorder characterized by megalencephaly, leukoencephalopathy, and Rosenthal fibers within astrocytes. This report describes the case of a female patient with sonography-detected ventriculomegaly at 32 weeks&rsquo; gestation and distinctive MR imaging features at 33 and 36 weeks&rsquo; gestation, at birth, and at 2 months of age, which led to the suggested diagnosis of Alexander disease. Molecular analysis confirmed a missense mutation in the <I>GFAP</I> gene. The literature contains little information on the fetal MR imaging findings that may allow prenatal diagnosis of AD.</P>
]]></description>
<dc:creator><![CDATA[Vazquez, E., Macaya, A., Mayolas, N., Arevalo, S., Poca, M.A., Enriquez, G.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1215</dc:identifier>
<dc:title><![CDATA[[PEDIATRICS] Neonatal Alexander Disease: MR Imaging Prenatal Diagnosis]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1975</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1973</prism:startingPage>
<prism:section>PEDIATRICS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1976?rss=1">
<title><![CDATA[[SPINE] Diffusion Tensor MR Imaging in Chronic Spinal Cord Injury]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1976?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Diffusion tensor MR imaging is emerging as an important tool for displaying anatomic changes in the brain after injury or disease but has been less widely applied to disorders of the spinal cord. The aim of this study was to characterize the diffusion properties of the entire human spinal cord in vivo during the chronic stages of spinal cord injury (SCI). These data provide insight into the structural changes that occur as a result of long-term recovery from spinal trauma.</P>
<P><B>MATERIALS AND METHODS:</B> Thirteen neurologically intact subjects and 10 subjects with chronic SCI (&gt;4 years postinjury) were enrolled in this study. A single-shot twice-refocused spin-echo diffusion-weighted echo-planar imaging pulse sequence was used to obtain axial images throughout the entire spinal cord (C1-L1) in &lt;60 minutes.</P>
<P><B>RESULTS:</B> Despite heterogeneity in SCI lesion severity and location, diffusion characteristics of the chronic lesion were significantly elevated compared with those of uninjured controls. Fractional anisotropy was significantly lower at the chronic lesion and appeared dependent on the completeness of the injury. Conversely, mean diffusivity measurements in the upper cervical spinal cord in subjects with SCI were significantly lower than those in controls. These trends suggest that the entire neuraxis may be affected by long-term recovery from spinal trauma.</P>
<P><B>CONCLUSION:</B> These results suggest that diffusion tensor imaging may be useful in the assessment of SCI recovery.</P>
]]></description>
<dc:creator><![CDATA[Ellingson, B.M., Ulmer, J.L., Kurpad, S.N., Schmit, B.D.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1272</dc:identifier>
<dc:title><![CDATA[[SPINE] Diffusion Tensor MR Imaging in Chronic Spinal Cord Injury]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1982</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1976</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1983?rss=1">
<title><![CDATA[[SPINE] Frequency and Outcome of Pulmonary Polymethylmethacrylate Embolism during Percutaneous Vertebroplasty]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1983?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> During percutaneous polymethylmethacrylate (PMMA) vertebroplasty (PV), PMMA cement may migrate into the venous system and subsequently be transported to the pulmonary arteries. Frequency, outcome, and imaging findings of PMMA pulmonary embolism are poorly understood. We retrospectively assessed the frequency and outcome of PMMA embolism during PV in a large patient cohort and evaluated the relationship of the volume of injected PMMA to the occurrence of pulmonary PMMA embolism.</P>
<P><B>MATERIALS AND METHODS:</B> Between 2001 and 2007, 532 osteoporotic compression fractures in 299 consecutive patients were treated with PV. PMMA embolism was defined as venous PMMA migration toward the lungs visible on biplane fluoroscopy during PV. CT was performed immediately and 1 year after PMMA migration.</P>
<P><B>RESULTS:</B> Venous PMMA migration occurred during 11 PVs in 11 patients (2.1%, 95% confidence interval, 1.1&ndash;3.7%). CT in 8 patients demonstrated small peripheral pulmonary PMMA emboli. All 11 patients remained asymptomatic during 1-year follow-up. Repeat CT scanning after 1 year in 6 patients demonstrated unchanged pulmonary PMMA deposits without late reactive changes. Mean injected cement volume in patients with and without PMMA embolism was not different (3.6 &plusmn; 1.06 mL versus 3.3 &plusmn; 1.16 mL, <I>P</I> = .43). Similar comparison for thoracic and thoracolumbar vertebrae yielded <I>P</I> values of .07 and .9.</P>
<P><B>CONCLUSION:</B> Pulmonary PMMA embolism during PV is an infrequent complication without permanent clinical sequelae. After 1 year, no pulmonary reaction was seen on CT. No definite relationship of PMMA emboli with injected cement volume could be established.</P>
]]></description>
<dc:creator><![CDATA[Venmans, A., Lohle, P.N.M., van Rooij, W.J., Verhaar, H.J.J., Mali, W.P.Th.M.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1269</dc:identifier>
<dc:title><![CDATA[[SPINE] Frequency and Outcome of Pulmonary Polymethylmethacrylate Embolism during Percutaneous Vertebroplasty]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1985</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1983</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1986?rss=1">
<title><![CDATA[[SPINE] Cement-Embolic Stroke Associated with Vertebroplasty]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1986?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Major neurologic morbidity and mortality with vertebroplasty are rare. We describe a 71-year-old woman who had a stroke approximately 30 minutes after vertebroplasty. Imaging revealed that bone cement had embolized to the left middle cerebral artery. Emergency embolectomy was attempted but was unsuccessful. This report emphasizes the need to be aware that intracranial embolization of polymethylmethacrylate can occur and describes management strategies to consider.</P>
]]></description>
<dc:creator><![CDATA[Marden, F.A., Putman, C.M.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1159</dc:identifier>
<dc:title><![CDATA[[SPINE] Cement-Embolic Stroke Associated with Vertebroplasty]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1988</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1986</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1989?rss=1">
<title><![CDATA[[SPINE] Brown-Sequard Syndrome Secondary to Spontaneous Bleed from Postradiation Cavernous Angiomas]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1989?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> The spontaneous occurrence of acute Brown-S&eacute;quard syndrome is an extremely rare event, with most reported cases being secondary to spontaneous epidural hematomas and spinal cord ischemia. We report a rare case of Brown-S&eacute;quard syndrome from spontaneous intraspinal hemorrhage in a patient with multiple cavernous angiomas in the spinal cord secondary to craniospinal radiation in childhood. Postulated mechanisms leading to the condition include postradiation molecular changes and venous occlusion.</P>
]]></description>
<dc:creator><![CDATA[Mathews, M.S., Peck, W.W., Brant-Zawadzki, M.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1158</dc:identifier>
<dc:title><![CDATA[[SPINE] Brown-Sequard Syndrome Secondary to Spontaneous Bleed from Postradiation Cavernous Angiomas]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1990</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1989</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1991?rss=1">
<title><![CDATA[[SPINE] Intraoperative 3T MR Imaging for Spinal Cord Tumor Resection: Feasibility, Timing, and Image Quality Using a "Twin" MR-Operating Room Suite]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1991?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We assessed feasibility, safety, and timing of an original intraoperative MR procedure in 3 cases of resection of spinal cord glioma by using a clinical 3T MR system connected to an adjacent operating room in a design being coined "twin" or "dual" MR&ndash;operating room suite.</P>
]]></description>
<dc:creator><![CDATA[Duprez, T.P., Jankovski, A., Grandin, C., Hermoye, L., Cosnard, G., Raftopoulos, C.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1134</dc:identifier>
<dc:title><![CDATA[[SPINE] Intraoperative 3T MR Imaging for Spinal Cord Tumor Resection: Feasibility, Timing, and Image Quality Using a "Twin" MR-Operating Room Suite]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1994</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1991</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1995?rss=1">
<title><![CDATA[[SPINE] Radiation-Induced Peripheral Nerve Neurofibromata in a Patient Receiving Hypofractionated Radiation Therapy]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1995?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> Radiation-induced peripheral nerve tumor, in particular a benign entity such as a neurofibroma, is rare, with only a few cases being reported so far. We demonstrate a case of radiation-induced neurofibromata along the left cervical nerve roots in a man with a background of localized targeted hypofractionated radiation therapy as adjuvant treatment for left cervical nodal metastasis complicating nasopharyngeal carcinoma. The toxicity of high-dose radiation in a hypofractionated regime is also stressed.</P>
]]></description>
<dc:creator><![CDATA[Lai, V., Wong, Y.C., Poon, W.L., Fu, Y.P., Lam, T.C., Yuen, S.C.]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1219</dc:identifier>
<dc:title><![CDATA[[SPINE] Radiation-Induced Peripheral Nerve Neurofibromata in a Patient Receiving Hypofractionated Radiation Therapy]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1997</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1995</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/10/1998?rss=1">
<title><![CDATA[[ACR APPROPRIATENESS CRITERIA] Focal Neurologic Deficit]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/10/1998?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Wippold, F.J., for the Expert Panel on Neurologic Imaging]]></dc:creator>
<dc:date>2008-11-13</dc:date>
<dc:title><![CDATA[[ACR APPROPRIATENESS CRITERIA] Focal Neurologic Deficit]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>10</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>2000</prism:endingPage>
<prism:publicationDate>2008-11-01</prism:publicationDate>
<prism:startingPage>1998</prism:startingPage>
<prism:section>ACR APPROPRIATENESS CRITERIA</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e80?rss=1">
<title><![CDATA[[LETTERS] Contrast Extravasation Predicts Hematoma Growth: Where to Now?]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e80?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Aviv, R.I., Gladstone, D., Goldstein, J., Flaherty, M., Broderick, J., Demchuk, A., for the Spot Sign for Predicting and Treating ICH Growth and Spot Sign Selection of ICH to Guide Hemostatic Therapy Investigators]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1140</dc:identifier>
<dc:title><![CDATA[[LETTERS] Contrast Extravasation Predicts Hematoma Growth: Where to Now?]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e80</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e80</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e81?rss=1">
<title><![CDATA[[LETTERS] MR Imaging Can Predict the Development of Nonalcoholic Wernicke Encephalopathy]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e81?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Ohira, M., Suzuki, S., Takahashi, S., Takahashi, K., Suzuki, N.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1144</dc:identifier>
<dc:title><![CDATA[[LETTERS] MR Imaging Can Predict the Development of Nonalcoholic Wernicke Encephalopathy]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e82</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e81</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e83?rss=1">
<title><![CDATA[[LETTERS] Reply:]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e83?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Zhong, C.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1146</dc:identifier>
<dc:title><![CDATA[[LETTERS] Reply:]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e83</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e83</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e84?rss=1">
<title><![CDATA[[LETTERS] Metronidazole-Induced and Wernicke Encephalopathy: Two Different Entities Sharing the Same Metabolic Pathway?]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e84?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Zuccoli, G., Pipitone, N., Santa Cruz, D.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1142</dc:identifier>
<dc:title><![CDATA[[LETTERS] Metronidazole-Induced and Wernicke Encephalopathy: Two Different Entities Sharing the Same Metabolic Pathway?]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e84</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e84</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e85?rss=1">
<title><![CDATA[[LETTERS] Reply:]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e85?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Na, D.G., Kim, E.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1145</dc:identifier>
<dc:title><![CDATA[[LETTERS] Reply:]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e85</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e85</prism:startingPage>
<prism:section>LETTERS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e86?rss=1">
<title><![CDATA[[BOOK REVIEWS] A Clinical Guide to Epileptic Syndromes and Their Treatment, 2nd ed.]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e86?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1231</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] A Clinical Guide to Epileptic Syndromes and Their Treatment, 2nd ed.]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e86</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e86</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e87?rss=1">
<title><![CDATA[[BOOK REVIEWS] The Stroke Book]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e87?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1032</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] The Stroke Book]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e87</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e87</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e88?rss=1">
<title><![CDATA[[BOOK REVIEWS] Neurodegeneration in Multiple Sclerosis]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e88?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1025</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Neurodegeneration in Multiple Sclerosis]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e89</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e88</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e90?rss=1">
<title><![CDATA[[BOOK REVIEWS] Radiology Business Practice: How to Succeed]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e90?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1061</dc:identifier>
<dc:title><![CDATA[[BOOK REVIEWS] Radiology Business Practice: How to Succeed]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e90</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e90</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/e91?rss=1">
<title><![CDATA[[BOOK REVIEWS] BOOKS RECEIVED]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/e91?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:title><![CDATA[[BOOK REVIEWS] BOOKS RECEIVED]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>e91</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>e91</prism:startingPage>
<prism:section>BOOK REVIEWS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1603?rss=1">
<title><![CDATA[[EDITORIALS] Identifying the Source of Printed Scientific Literature]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1603?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Castillo, M.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1245</dc:identifier>
<dc:title><![CDATA[[EDITORIALS] Identifying the Source of Printed Scientific Literature]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1604</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>1603</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1604?rss=1">
<title><![CDATA[[EDITORIALS] What is All of the Hype About?]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1604?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Cloft, H.J.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1228</dc:identifier>
<dc:title><![CDATA[[EDITORIALS] What is All of the Hype About?]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1604</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>1604</prism:startingPage>
<prism:section>EDITORIALS</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1605?rss=1">
<title><![CDATA[[REVIEW ARTICLES] Metastatic Spinal Lesions: State-of-the-Art Treatment Options and Future Trends]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1605?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> The purpose of this article is to review the current state of the art for treating symptomatic spinal fractures associated with malignant lesions and to present potential future trends in treatments for this patient population. Epidemiology, clinical presentation, and biomechanical ramifications of these lesions are summarized and treatment regimes, clinical outcomes, and complications and technical issues associated with treatments are presented. Potential future trends and new technologies for performing vertebral body augmentation in patients with metastatic spinal lesions are also discussed.</P>
]]></description>
<dc:creator><![CDATA[Georgy, B.A.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1137</dc:identifier>
<dc:title><![CDATA[[REVIEW ARTICLES] Metastatic Spinal Lesions: State-of-the-Art Treatment Options and Future Trends]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1611</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>1605</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1612?rss=1">
<title><![CDATA[[REVIEW ARTICLES] MR Imaging Findings in Hepatic Encephalopathy]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1612?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> The term hepatic encephalopathy (HE) includes a spectrum of neuropsychiatric abnormalities occurring in patients with liver dysfunction. Most cases are associated with cirrhosis and portal hypertension or portal-systemic shunts, but the condition can also be seen in patients with acute liver failure and, rarely, with portal-systemic bypass and no associated intrinsic hepatocellular disease. Although HE is a clinical condition, several neuroimaging techniques, particularly MR imaging, may eventually be useful for the diagnosis because they can identify and measure the consequences of central nervous system (CNS) increase in substances that under normal circumstances, are efficiently metabolized by the liver. Classic MR imaging abnormalities include high signal intensity in the globus pallidum on T1-weighted images, likely a reflection of increased tissue concentrations of manganese, and an elevated glutamine/glutamate peak coupled with decreased myo-inositol and choline signals on proton MR spectroscopy, representing disturbances in cell-volume homeostasis secondary to brain hyperammonemia. Recent data have shown that white matter abnormalities, also related to increased CNS ammonia concentration, can also be detected with several MR imaging techniques such as magnetization transfer ratio measurements, fast fluid-attenuated inversion recovery sequences, and diffusion-weighted images. All these MR imaging abnormalities, which return to normal with restoration of liver function, probably reflect the presence of mild diffuse brain edema, which seems to play an essential role in the pathogenesis of HE. It is likely that MR imaging will be increasingly used to evaluate the mechanisms involved in the pathogenesis of HE and to assess the effects of therapeutic measures focused on correcting brain edema in these patients.</P>
]]></description>
<dc:creator><![CDATA[Rovira, A., Alonso, J., Cordoba, J.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1139</dc:identifier>
<dc:title><![CDATA[[REVIEW ARTICLES] MR Imaging Findings in Hepatic Encephalopathy]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1621</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>1612</prism:startingPage>
<prism:section>REVIEW ARTICLES</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1622?rss=1">
<title><![CDATA[[SPINE] Pain Relief following Vertebroplasty in Patients With and Without Localizing Tenderness on Palpation]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1622?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B> Focal point tenderness over the fractured level is believed to be a necessary criterion for performing vertebroplasty. The purpose of this study was to explore whether the presence of focal-point tenderness over a fracture treated with vertebroplasty predicts superior clinical outcome as compared with outcomes in patients without such tenderness.</P>
<P><B>MATERIALS AND METHODS:</B> In this retrospective study, we divided patients into 3 groups on the basis of pain patterns noted during history and physical examination before an initial vertebroplasty in 534 consecutive patients. Group 1 comprised 373 (70%) of 534 patients with focal-point tenderness over the treated fractures. Group 2 comprised 119 (22%) patients with focal-point tenderness over the treated fractures as well as subjective off-midline pain or focal tenderness to palpation over nontreated vertebrae. Group 3 comprised 42 (8%) patients without focal-point tenderness over the treated fractures but with subjective off-midline pain or tenderness to palpation over nontreated vertebrae. Outcomes included pain at rest and with activity as well as the Roland-Morris Disability Questionnaire score. Statistical tools included the 2-tailed <I>t</I> test with a Bonferroni adjustment.</P>
<P><B>RESULTS:</B> Baseline pain at rest and with activity was not different among groups, but the proportion of group 3 patients maintained on a narcotic anesthesia preprocedure was less than that of groups 1 and 2 (<I>P</I> = .02 compared with both groups). Group 3 achieved significantly lower pain scores at rest at 1 month (<I>P</I> &lt; .0001 compared with group 1 and <I>P</I> &lt; .001 compared with group 2).</P>
<P><B>CONCLUSION:</B> The presence of focal-point tenderness does not predict superior clinical response following vertebroplasty compared with the absence of focal tenderness. Even patients without focal tenderness may benefit from vertebroplasty.</P>
]]></description>
<dc:creator><![CDATA[Rad, A. E., Kallmes, D.F.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1186</dc:identifier>
<dc:title><![CDATA[[SPINE] Pain Relief following Vertebroplasty in Patients With and Without Localizing Tenderness on Palpation]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1626</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>1622</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1627?rss=1">
<title><![CDATA[[SPINE] Emergent Image-Guided Treatment of a Large CSF Leak to Reverse "In-Extremis" Signs of Intracranial Hypotension]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1627?rss=1</link>
<description><![CDATA[
<P><B>SUMMARY:</B> We report the use of an emergent, targeted fibrin spinal epidural blood patch with subarachnoid saline infusion to rapidly reverse "in-extremis" clinical and imaging signs of posterior-fossa coning brought about by acute-on-chronic intracranial hypotension, itself consequent to a cervicothoracic CSF leak. Treatment resulted in a dramatic recovery and eventual discharge with return to normal lifestyle and occupation. The clinical and imaging danger signs are reviewed; fibrin patch technique and potential pitfalls in postprocedure management are analyzed.</P>
]]></description>
<dc:creator><![CDATA[Lasboo, A.A., Hurley, M.C., Walker, M.T., Surdell, D., Song, J.K., Rosenow, J.M., Shaibani, A.]]></dc:creator>
<dc:date>2008-10-08</dc:date>
<dc:identifier>info:doi/10.3174/ajnr.A1157</dc:identifier>
<dc:title><![CDATA[[SPINE] Emergent Image-Guided Treatment of a Large CSF Leak to Reverse "In-Extremis" Signs of Intracranial Hypotension]]></dc:title>
<dc:publisher>American Society of Neuroradiology</dc:publisher>
<prism:number>9</prism:number>
<prism:volume>29</prism:volume>
<prism:endingPage>1629</prism:endingPage>
<prism:publicationDate>2008-10-01</prism:publicationDate>
<prism:startingPage>1627</prism:startingPage>
<prism:section>SPINE</prism:section>
</item>

<item rdf:about="http://www.ajnr.org/cgi/content/full/29/9/1630?rss=1">
<title><![CDATA[[BRAIN] Differentiation Between Classic and Atypical Meningiomas with Use of Diffusion Tensor Imaging]]></title>
<link>http://www.ajnr.org/cgi/content/full/29/9/1630?rss=1</link>
<description><![CDATA[
<P><B>BACKGROUND AND PURPOSE:</B>The differentiation between classic and atypical meningiomas may have implications in preoperative planning but may not be possible on the basis of conventional MR imaging. Our hypothesis was that classic and atypical meningiomas have different patterns of intratumoral water diffusion that will allow for differentiation between them.</P>
<P><B>MATERIALS AND METHODS:</B>Preoperative diffusion tensor imaging (DTI) was performed in 12 classic and 12 atypical meningiomas. Signal intensity of solid-enhancing tumor