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Primary Brain Tumours in Adults
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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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The Autosomal Recessive Cerebellar Ataxias
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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The Tuberous Sclerosis Complex
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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CSF Evaluation in Primary CNS Lymphoma Patients by PCR of the CDR III IgH Genes
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Sickle Cell Disease: The Neurological Complications
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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Impact of the Human Genome Projects and Identification of a Stroke Gene
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Molecular Basis of the Neurodegenerative Disorders
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Prader-Willi and Angelman Syndromes
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The Muscular Dystrophies
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Investigation of Muscle Disease
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Clinical Genetics in Neurological Disease
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Trinucleotide Repeat Expansion in Neurological Disease
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