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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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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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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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The Autosomal Recessive Cerebellar Ataxias
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A 23-Year-Old Man With Seizures and Visual Deficit
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Mitochondrial DNA and Disease
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Hereditary Hemorrhagic Telangiectasia
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Leber's Hereditary Optic Neuropathy, New Genetic Considerations
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Gene Therapy for Neurologic Disease
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Intracranial Neoplasms and Paraneoplastic Disorders
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Spinal Muscular Atrophy A Timely Review
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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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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Fragile X Premutation With Atypical Symptoms at Onset
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Unusual Variants of Alexander's Disease
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Aromatic L-Amino Acid Decarboxylase Deficiency
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
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Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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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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The Muscular Dystrophies
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The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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