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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Spinal Muscular Atrophy A Timely Review
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Neurofibromatosis Type 2
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
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von Hippel-Lindau Disease
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Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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Causal Heterogeneity in Isolated Lissencephaly
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Muscular Dystrophies
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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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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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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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The Tuberous Sclerosis Complex
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Aromatic L-Amino Acid Decarboxylase Deficiency
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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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What Level of Care for the Neurofibromatoses?
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Molecular Basis of the Neurodegenerative Disorders
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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The Genetics of Alzheimer Disease, Current Status and Future Prospects
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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Exploring the Etiology of Alzheimer Disease Using Molecular Genetics
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The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
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von Hippel-Lindau Disease
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Trinucleotide Repeat Expansion in Neurological Disease
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Molecular Genetics in Neurology
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Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
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Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
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Wilson Disease
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Clinicopath Conf
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Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
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More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation
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