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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Neuroradiologic Aspects of Chester-Erdheim Disease
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Cogan's Syndrome:18 Cases & a Review of the Literature
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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A Family with Hereditary Ataxia:HLA Typing
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Dominant Spinopontine Atrophy
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Physostigmine in Familial Ataxias
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Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
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Trichinosis with Central Nervous System Involvement
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