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Showing articles 0 to 9 of 9 Filter Applied: ataxia,hereditary (Click to remove) Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983 A 48-Year-Old Man With Spasticity and Progressive Ataxia Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023 Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017 Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment Brain 130:2484-2493, Jen, J.C.,et al, 2007 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995 Dominant Spinopontine Atrophy Arch Neurol 35:156, Pogacar,S.,et al, 1978 Azorean Disease of the Nervous System NEJM 296:1505, Romanul,F.C.A.,et al, 1977 Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass Neurol 22:49, Nakano,K.K.,et al, 1972 Showing articles 0 to 9 of 9