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Showing articles 0 to 8 of 8 Filter Applied: gene mutation (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 Neurodegeneration with Brain Iron Accumulation AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019 Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 NEJM 370:911-920, Zhou, Q.,et al, 2014 Genetic Aspects of Alzheimer Disease The Neurologist 15:80-86, Williamson,J.,et al, 2009 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease Lancet 365:410-412, Nichols, W.C., et al, 2005 Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration Ann Neurol 57:738-741,613, Castelnau,P.,et al, 2005 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Showing articles 0 to 8 of 8