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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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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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Mitochondrial DNA and Disease
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Hereditary Hemorrhagic Telangiectasia
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Causal Heterogeneity in Isolated Lissencephaly
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Primary Brain Tumours in Adults
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Pediatric Leigh Syndrome
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Intracranial Neoplasms and Paraneoplastic Disorders
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Detection of Human Herpesvirus-6 in Cerebrospinal Fluid of Patients with Encephalitis
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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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The Tuberous Sclerosis Complex
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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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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Prader-Willi and Angelman Syndromes
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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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Human Prion Diseases
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Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
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Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
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