A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Primary Brain Tumours in Adults
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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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Clinicopathologic Conference, Oligdendroglioma II/IV with IDH1 R132H mutation and codelation of 1p and 19q
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Intracranial Neoplasms and Paraneoplastic Disorders
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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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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Neurofibromatosis Type 2
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Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment
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The Tuberous Sclerosis Complex
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Hereditary Hemorrhagic Telangiectasia
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Causal Heterogeneity in Isolated Lissencephaly
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Pediatric Leigh Syndrome
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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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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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Tuberous Sclerosis
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Whipples Disease
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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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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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CSF Evaluation in Primary CNS Lymphoma Patients by PCR of the CDR III IgH Genes
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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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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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Investigation of Muscle Disease
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Mitochondrial DNA and Disease
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Human Prion Diseases
Ann Neurol 35:385-395, Prusiner,S.B.&Hsiao,K.K., 1994
Trinucleotide Repeat Expansion in Neurological Disease
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Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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Molecular Genetics in Neurology
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Gene Therapy for Neurologic Disease
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DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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