Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Neurologic Aspects of Cobalamin Deficiency
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The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
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Subacute Combined Degeneration of the Spinal Cord
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