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Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
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Clinicopath Conf, Infantile Krabbe Disease
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Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
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