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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Clinical and Magnetic Resonance Features of the Classic & Akinetic-Rigid Variants of Huntington's Dis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Blepharospasm with Bilateral Basal Ganglia Infarction
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Function of the Basal Ganglia
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Corticodentatonigral Degeneration with Neuronal Achromasia
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Progressive Supranuclear Palsy: A Current Review
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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Severe Tetanus in Immunized Patients with High Anti-Tetanus Titers
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Missed Neuroleptic Malignant Syndrome
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Cortical-Basal Ganglionic Degeneration
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Diffuse Lewy Body Disease and Progressive Dementia
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