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Zika Virus Associated with Microcephaly
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A 23-Year-Old Man With Seizures and Visual Deficit
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Tuberous Sclerosis
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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The Tuberous Sclerosis Complex
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Mitochondrial DNA Polymerase-y and Human Disease
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Prader-Willi and Angelman Syndromes
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Mitochondrial DNA and Disease
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Causal Heterogeneity in Isolated Lissencephaly
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Pediatric Leigh Syndrome
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Ehlers-Danlos Syndromes
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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Diagnosis and New Treatment in Muscle Channelopathies
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Neurofibromatosis Type 2
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Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
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Spinal Muscular Atrophy
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Whipples Disease
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
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Sickle Cell Disease: The Neurological Complications
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Impact of the Human Genome Projects and Identification of a Stroke Gene
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Clinical and Genetic Aspects of Distal Myopathies
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What Level of Care for the Neurofibromatoses?
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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