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Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment
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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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Primary Brain Tumours in Adults
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Pediatric Leigh Syndrome
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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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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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A 23-Year-Old Man With Seizures and Visual Deficit
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Whipples Disease
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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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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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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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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
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Investigation of Muscle Disease
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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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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Clinical Consequences of Isolating the Gene for Huntington's Disease
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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Wilson Disease
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