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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Neurodegeneration with Brain Iron Accumulation
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Thyrotoxic Periodic Paralysis
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Spinal Muscular Atrophy
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Duchenne Muscular Dystrophy
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Huntington Disease: Clinical Features and Diagnosis
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Molybdenum Cofactor Deficiency
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Red Papules on the Tongue of a Patient with Hemiparesis
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A 52-year-old Woman with Progressive Proximal Weakness
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Sturge-Weber Syndrome
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The Limbic-Girdle Muscular Dystrophies
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Sturge-Weber Syndrome
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
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Genetic Aspects of Alzheimer Disease
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
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Dystonia
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Parkinsons Disease and Genetics
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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