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Cerebellar Ataxia in Children
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Spinocerebellar Ataxia Type 8
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Trinucleotide Repeat Expansion in Neurological Disease
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Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
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Retinitis Pigmentosa
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Cranial Computerized Tomography & Marie's Ataxia
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Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
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