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Showing articles 0 to 11 of 11 Filter Applied: cerebellar atrophy,primary (Click to remove) Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings AJNR 18:583-586, Tzeng,B-C.,et al, 1997 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction. AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002 Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies Arch Neurol 58:225-230, Honorat,J.,et al, 2001 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 Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995 Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum Neurol 39:1446-1452, Farlow,M.R.,et al, 1989 Magnetic Resonance Imaging in Familial Paroxysmal Ataxia Arch Neurol 45:547-549, Vighetto,A.,et al, 1988 Physostigmine in Familial Ataxias Neurol 27:70, Kark,R.A.,et al, 1977 Showing articles 0 to 11 of 11