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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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A Teenager with Persistent Headache
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Essential Tremor
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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Cerebral Amyloid Angiopathy
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Seizures on Hearing the Alarm Clock
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Autonomic Peripheral Neuropathy
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Treatment of Sporadic Hemiplegic Migraine with Calcium-Channel Blocker Verapamil
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Cardiac Dysfunction in Neuromuscular Diseases
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Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Niemann-Pick Disease Type C from Bench to Bedside
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
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The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
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Real and Imagined Clinicopathological Limits of"Prior Dementia"
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Infectious Prions or Cytotoxic Metabolites?
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Genetic Susceptibility in Familial Multiple Sclerosis not Linked to the Myelin Basic Protein Gene
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Choroido-Cerebral Calcification Syndrome with Retardation
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Protein S Deficiency in Middle-Aged Women with Stroke
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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Analysis of the Prion Protein Gene in Thalamic Dementia
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Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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The Spongiform Encephalopathies, Editorial
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Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
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Inherited Human Prion Diseases
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