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The Genetics of Alzheimer Disease, Current Status and Future Prospects
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Exploring the Etiology of Alzheimer Disease Using Molecular Genetics
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Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
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Spinal Muscular Atrophy
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
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Spinal Muscular Atrophy A Timely Review
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Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
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Neurofibromatosis Type 2
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Neurofibromatosis
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Spinal Muscular Atrophy
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Autonomic Peripheral Neuropathy
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Phaeochromocytoma
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Genetic Factors in Alzheimer's Disease
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The Clinicopathological Spectrum of Rosenthal Fibre Encephalopathy and Alexanders Disease: A Case Report and Review of the Literature
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
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Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
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Multiple Sclerosis
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What Level of Care for the Neurofibromatoses?
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Trinucleotide Repeat Expansion in Neurological Disease
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Persistence of Initial Infection in Recurrent Cryptococcus Neuformans Meningitis
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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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Lisch Nodules in Neurofibromatosis Type I
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Neurofibromatosis Type I in Children
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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AIDS-Assoc Progressive Multifocal Leukoencephalopathy (PML) :Comparison to Non-AIDS PML
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Genetic Markers for Neurofibromatosis
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Neurofibromatosis
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Neurofibromatosis
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Mendelian Etiologies of Stroke
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