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Familial Tourette Syndrome
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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The Genetics of Alzheimer Disease, Current Status and Future Prospects
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Parental Transmission in Huntington's Disease
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Neonatal Seizures
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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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Muscular Dystrophies
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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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Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures
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The Limbic-Girdle Muscular Dystrophies
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Sturge-Weber Syndrome
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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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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