Enter your terms above and click the 'Search' button.

Showing articles 0 to 8 of 8 Filter Applied: spinocerebellar ataxia (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 A 28-Year-Old Woman with Vision Loss and an Unusual Gait Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Autonomic Dysfunction in Machado-Joseph Disease Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005 Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families Neurol 51:1666-1671, Moseley,M.L.,et al, 1998 The Inherited Ataxias and the New Genetics JNNP 61:327-332, Hammans,S.R., 1996 Isolated Vitamin E Deficiency Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996 Showing articles 0 to 8 of 8