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Showing articles 0 to 12 of 12 Filter Applied: cerebellar atrophy,primary (Click to remove) Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017 Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination NEJM 368:1992-2003, Margolin, D.,et al, 2013 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion Neruol 56:299-303,287, O'Hearn,E.,et al, 2001 Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis Ann Neurol 43:288-296, Onokera,O.,et al, 1998 Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease BMJ 315:856-857, Fox,N.C.,et al, 1997 Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia Neurol 43:318-325, Wullner,U.,et al, 1993 Chronic Neurodegenerative Disease Associated with HTLV-II Infection Lancet 339:645-646, Hjelle,B.,et al, 1992 Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992 The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990 Magnetic Resonance Imaging in Familial Paroxysmal Ataxia Arch Neurol 45:547-549, Vighetto,A.,et al, 1988 Showing articles 0 to 12 of 12