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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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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Paroxysmal Cerebellar Ataxia
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Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
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Dominant Spinopontine Atrophy
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Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977
Machado Disease-a Hereditary Ataxia in Portuguese Emigrants to Mass
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