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A 23-Year-Old Man With Seizures and Visual Deficit
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Neuroimaging Findings in Human Prion Disease
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Retinocochleocerebral Vasculopathy
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Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
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Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
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Familial Chorea & Myoclonus Epilepsy
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Huntington Disease: Clinical Features and Diagnosis
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Chorea Resulting From Paraneoplastic Striatal Encephalitis
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Mitochondrial DNA and Disease
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Neurologic Manifestations of Giant Cell Arteritis
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Alcoholic Dementia:A Hypothesis
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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
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Idiopathic Hypoparathyroidism Presenting as Dementia
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Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
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Catecholamines & Neurologic Diseases
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Hepatic Encephalopathy:Current Status
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