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Showing articles 0 to 8 of 8 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 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 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 A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders Neurol Sci 23:145-151, Vianello,M.,et al, 2002 Chronic Neurodegenerative Disease Associated with HTLV-II Infection Lancet 339:645-646, Hjelle,B.,et al, 1992 Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome) Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990 Showing articles 0 to 8 of 8