Multiple-System Atrophy
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Neurologic Aspects of Cobalamin Deficiency
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The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
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Familial Inverted Choreoathetosis
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Chronic Meningitis
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Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
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