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Mitochondrial DNA and Disease
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Hereditary Hemorrhagic Telangiectasia
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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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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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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Molecular Genetics in Neurology
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Wilson Disease
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Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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Intracranial Neoplasms and Paraneoplastic Disorders
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The Autosomal Recessive Cerebellar Ataxias
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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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Fragile X Premutation With Atypical Symptoms at Onset
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Unusual Variants of Alexander's Disease
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Gene Transfer for Neurologic Disease
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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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Alzheimer Disease
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Sickle Cell Disease: The Neurological Complications
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Impact of the Human Genome Projects and Identification of a Stroke Gene
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The Brain Code in Health and Disease
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Prader-Willi and Angelman Syndromes
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The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
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Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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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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Trinucleotide Repeat Expansion in Neurological Disease
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The DNA Laboratory and Neurolgoical Practice
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
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Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
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