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The Tuberous Sclerosis Complex
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Primary Brain Tumours in Adults
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Neurofibromatosis Type 2
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Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment
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Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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Mitochondrial DNA and Disease
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Hereditary Hemorrhagic Telangiectasia
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Molecular Genetics in Neurology
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Gene Therapy for Neurologic Disease
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Pediatric Leigh Syndrome
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Ehlers-Danlos Syndromes
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Zika Virus Associated with Microcephaly
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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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Recent Insights into Cerebral Cavernous Malformations: The Molecular Genetics of CCM
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Detection of Human Herpesvirus-6 in Cerebrospinal Fluid of Patients with Encephalitis
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Diagnosis and New Treatment in Muscle Channelopathies
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A 23-Year-Old Man With Seizures and Visual Deficit
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Spinal Muscular Atrophy
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Mitochondrial DNA Polymerase-y and Human 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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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
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Causal Heterogeneity in Isolated Lissencephaly
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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