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Showing articles 0 to 6 of 6 Filter Applied: spinocerebellar ataxia type 1 (Click to remove) Trinucleotide Repeat Expansion in Neurological Disease Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994 Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy Neurol 55:527-532, Gilman,S. et al, 2000 Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy JNNP 65:65-71, Schrag,A.,et al, 1998 Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families Neurol 51:1666-1671, Moseley,M.L.,et al, 1998 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 Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue Neurol 45:1-5, Rosenberg,R.N., 1995 Showing articles 0 to 6 of 6