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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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Mitochondrial DNA and Disease
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Hereditary Hemorrhagic Telangiectasia
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Clinicopath Conf
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Genetice of Cerebrovascular Disease
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Zika Virus Associated with Microcephaly
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Pediatric Leigh Syndrome
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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A 23-Year-Old Man With Seizures and Visual Deficit
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Tuberous Sclerosis
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Whipples Disease
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Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment
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Unusual Variants of Alexander's Disease
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Prader-Willi and Angelman Syndromes
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
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Causal Heterogeneity in Isolated Lissencephaly
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