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Showing articles 0 to 9 of 9 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 Neuropsychological Changes in Olivopontocerebellar Atrophy Arch Neurol 47:997-1001, Berent,S.,et al, 1990 Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen Arch Neurol 42:757-758, Trauner,D.A., 1985 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 Clinicopathological Study of 35 Cases of Multiple System Atrophy JNNP 58:160-166, Wenning,G.K.,et al, 1995 PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995 Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology JNNP 53:297-305, Klockgether,T.,et al, 1990 Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography Ann Neurol 23:223-230, Gilman,S.,et al, 1988 Showing articles 0 to 9 of 9