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Showing articles 0 to 6 of 6 Filter Applied: spinocerebellar ataxia type 1 (Click to remove) 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 The Role of Glutamate in Neurotransmission & in Neurologic Disease Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986 Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen Arch Neurol 42:757-758, Trauner,D.A., 1985 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