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Showing articles 0 to 9 of 9 Filter Applied: trinucleotide repeats (Click to remove) Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp Neurol 45:24-30, Genis,D.,et al, 1995 A 48-Year-Old Man With Spasticity and Progressive Ataxia Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023 Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady JAMA Neurol 74:238-241, Dubey, D.,et al, 2017 Huntington Disease: Clinical Features and Diagnosis UptoDate Dec 2017, Oksana Suchowersky, 2017 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Brugada Syndrome in Spinal and Bulbar Muscular Atrophy Neurol 82:1813-1821, Araki, A.,et al, 2014 Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy) Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014 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 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Showing articles 0 to 9 of 9