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Causal Heterogeneity in Isolated Lissencephaly
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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Detection of Human Herpesvirus-6 in Cerebrospinal Fluid of Patients with Encephalitis
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Whipples Disease
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Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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Prion Dementia Without Characteristic Pathology
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Inherited Human Prion Diseases
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Pediatric Leigh Syndrome
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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The Muscular Dystrophies
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Investigation of Muscle Disease
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Mitochondrial DNA and Disease
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Hereditary Hemorrhagic Telangiectasia
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Human Prion Diseases
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Congenital Myopathies
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The Nondystrophic Myotonias
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
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