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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Analysis of the Prion Protein Gene in Thalamic Dementia
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Clinical Reasoning: A Teenager with Left Arm Weakness
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Tourette's Syndrome:A Model Neuropsychiatric Disorder
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Molecular Genetics in Neurology
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Hematologic Disorders and Ischemic Stroke
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
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Clinicopathological Conference
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Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
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Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
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