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Showing articles 0 to 10 of 10 Filter Applied: cerebellar atrophy,primary (Click to remove) Complex Ataxia Neurol 95:136-141, Abkur, T.,et al, 2020 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 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 Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria Neurol 52:1472-1478, Nardocci,N.,et al, 1999 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 Showing articles 0 to 10 of 10