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Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Chronic Neurodegenerative Disease Associated with HTLV-II Infection
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Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
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Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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