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An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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The Motor Disorder of Multiple System Atrophy
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Neurologic Sequelae of Chronic Solvent Vapor Abuse
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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
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Neurologic Complications of Primary Sjogren's Syndrome
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Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
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Neurologic Abnormalities of Lyme Disease
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