Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Corticodentatonigral Degeneration with Neuronal Achromasia
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CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
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Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
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A pedigree of Amyotrophic Chorea With Acantho-cytosis
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