Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Huntington Disease: Clinical Features and Diagnosis
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hypoxic-Ischemic Damage of the Basal Ganglia
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
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A pedigree of Amyotrophic Chorea With Acantho-cytosis
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Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
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Familial Chorea & Myoclonus Epilepsy
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Neurologic Manifestations in Sarcoidosis
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