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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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Neurofibromatosis Type 2
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Whipples Disease
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The Tuberous Sclerosis Complex
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Mitochondrial DNA and Disease
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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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Diagnosis and New Treatment in Muscle Channelopathies
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Spinal Muscular Atrophy
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Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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Hereditary Hemorrhagic Telangiectasia
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Myotonic Dystrophy
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Ehlers-Danlos Syndromes
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Diagnosis and Misdiagnosis of Adult Neuronal Ceroid Lipofuscinosis
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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The Autosomal Recessive Cerebellar Ataxias
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Spinal Muscular Atrophy A Timely Review
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Tuberous Sclerosis
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Aromatic L-Amino Acid Decarboxylase Deficiency
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Pathogenetic Mechanisms of Parkin in Parkinson's Disease
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Alzheimer's Disease and Parkinson's Disease
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Alzheimer Disease
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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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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Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
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The Muscular Dystrophies
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