OtherACR CRITERIA
Ataxia
J.A. Brunberg for the Expert Panel on Neurologic Imaging
American Journal of Neuroradiology August 2008, 29 (7) 1420-1422;
References
- ↵Gilman S, Gelb DJ. Disorders of the cerebellum. In: Griggs RC, Joynt RJ, eds. Baker's Clinical Neurology: Lippincott Williams & Wilkins,2003
- ↵Abel TW, Baker SJ, Fraser MM, et al. Lhermitte-Duclos disease: a report of 31 cases with immunohistochemical analysis of the PTEN/AKT/mTOR pathway. J Neuropathol Exp Neurol 2005;64:341–49
- ↵
- ↵Kataoka S, Hori A, Shirakawa T, et al. Paramedian pontine infarction. Neurological/topographical correlation. Stroke 1997;28:809–15
- ↵Cormier PJ, Long ER, Russell EJ. MR imaging of posterior fossa infarctions: vascular territories and clinical correlates. Radiographics 1992;12:1079–96
- ↵Shah GV, Quint DJ, Trobe JD. Magnetic resonance imaging of suspected cervicocranial arterial dissections. J Neuroophthalmol 2004;24:315–18
- ↵Kumar N, Cohen-Gadol AA, Wright RA, et al. Superficial siderosis. Neurology 2006;66:1144–52
- ↵Garg M, Gupta RK, Husain M, et al. Brain abscesses: etiologic categorization with in vivo proton MR spectroscopy. Radiology 2004;230:519–27
- ↵Kato Z, Kozawa R, Teramoto T, et al. Acute cerebellitis in primary human herpesvirus-6 infection. Eur J Pediatr 2003;162:801–03
- ↵
- ↵De Bruecker Y, Claus F, Demaerel P, et al. MRI findings in acute cerebellitis. Eur Radiol 2004;14:1478–83
- ↵
- ↵Mondejar RR, Santos JM, Villalba EF. MRI findings in a remitting-relapsing case of Bickerstaff encephalitis. Neuroradiology 2002;44:411–14
- ↵
- ↵Inoue N, Ichimura H, Goto S, et al. MR imaging findings of spinal posterior column involvement in a case of Miller Fisher syndrome. AJNR Am J Neuroradiol 2004;25:645–48
- ↵Terry JB, Rosenberg RN. Frontal lobe ataxia. Surg Neurol 1995;44:583–88
- ↵Ge Y. Multiple sclerosis: the role of MR imaging. AJNR Am J Neuroradiol 2006;27:1165–76
- ↵Patel S, Barkovich AJ. Analysis and classification of cerebellar malformations. AJNR Am J Neuroradiol 2002;23:1074–87
- ↵Alorainy IA, Sabir S, Seidahmed MZ, et al. Brain stem and cerebellar findings in Joubert syndrome. J Comput Assist Tomogr 2006;30:116–21
- ↵Valente EM, Marsh SE, Castori M, et al. Distinguishing the four genetic causes of Jouberts syndrome-related disorders. Ann Neurol 2005;57:513–19
- ↵Mercuri E, He J, Curati WL, et al. Cerebellar infarction and atrophy in infants and children with a history of premature birth. Pediatr Radiol 1997;27:139–43
- ↵Himmelmann K, Hagberg G, Beckung E, et al. The changing panorama of cerebral palsy in Sweden. IX. Prevalence and origin in the birth-year period 1995–1998. Acta Paediatr 2005;94:287–94
- ↵Berciano J, Boesch S, Perez-Ramos JM, et al. Olivopontocerebellar atrophy: Toward a better nosological definition. Mov Disord 2006;21:1607–13. Review.
- ↵Kerber KA, Jen JC, Perlman S, et al. Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations. J Neurol Sci 2005;238:41–45
- ↵Koide R, Onodera O, Ikeuchi T, et al. Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings. Neurology 1997;49:1605–12
- ↵Bhidayasiri R, Perlman SL, Pulst SM, et al. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature. Arch Neurol 2005;62:1865–69
- Butch AW, Chun HH, Nahas SA, et al. Immunoassay to measure ataxia-telangiectasia mutated protein in cellular lysates. Clin Chem 2004;50:2302–08
- ↵Tavani F, Zimmerman RA, Berry GT, et al. Ataxia-telangiectasia: the pattern of cerebellar atrophy on MRI. Neuroradiology 2003;45:315–19
- ↵Brunberg JA, Jacquemont S, Hagerman RJ, et al. Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction. AJNR Am J Neuroradiol 2002;23:1757–66
- Hagerman RJ, Leehey M, Heinrichs W, et al. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 2001;57:127–30
- ↵Verkerk AJ, Pieretti M, Sutcliffe JS, et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991;65:905–14
- ↵Geser F, Wenning GK. The diagnosis of multiple system atrophy. J Neurol 2006;253 Suppl 3:iii2–iii15
- ↵Browne DL, Gancher ST, Nutt JG, et al. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nat Genet 1994;8:136–40
- ↵Jen JC, Wan J, Palos TP, et al. Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures. Neurology 2005;65:529–34
- ↵Bassi SS, Bulundwe KK, Greeff GP, et al. MRI of the spinal cord in myelopathy complicating vitamin B12 deficiency: two additional cases and a review of the literature. Neuroradiology 1999;41:271–74
In this issue
Advertisement
Ataxia
J.A. Brunberg
American Journal of Neuroradiology Aug 2008, 29 (7) 1420-1422;
Jump to section
Related Articles
- No related articles found.
Cited By...
- No citing articles found.
This article has not yet been cited by articles in journals that are participating in Crossref Cited-by Linking.
Similar Articles
Advertisement