Somatic Mutations in Cerebral Cortical Malformations
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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"Disappearing Infarct" Is Late-Onset MELAS
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Pediatric Leigh Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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Hydrocephalus in Children
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Sturge-Weber Syndrome
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Neuroimaging Findings in Human Prion Disease
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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X-Linked Malformation of Neuronal Migration
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Molecular Genetics in Neurology
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Hypomelanosis of Ito
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Causal Heterogeneity in Isolated Lissencephaly
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
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