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Amyotrophic Lateral Sclerosis
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Medical Aspects of the Persistent Vegetative State
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Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
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Corticodentatonigral Degeneration with Neuronal Achromasia
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