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Showing articles 0 to 6 of 6 Filter Applied: ataxia,hereditary (Click to remove) 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 Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders Arch Neurol 61:875-880, Smith,C.O.,et al, 2004 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families Ann Neurol 10:355-363, Colan,R.V.,et al, 1981 A Family with Hereditary Ataxia:HLA Typing Neurol 30:12-20, Nino,H.E.,et al, 1980 Dominant Spinopontine Atrophy Arch Neurol 35:156, Pogacar,S.,et al, 1978 Showing articles 0 to 6 of 6