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Showing articles 0 to 7 of 7 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 Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria Neurol 52:1472-1478, Nardocci,N.,et al, 1999 Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity Neurol 49:1026-1030, Saiz,A.,et al, 1997 Complex Ataxia Neurol 95:136-141, Abkur, T.,et al, 2020 An Unusual Fundus Finding in a Teenage Girl JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018 Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Showing articles 0 to 7 of 7