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Angelman Syndrome: Clinical Profile
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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Parkinson Disease Subtypes
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The Autosomal Recessive Cerebellar Ataxias
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Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
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Presynaptic Dopaminergic Deficits in Lesch-Nyhan Disease
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Cerebral Involvement in McLeod Syndrome
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Progressive Language Disorder Due to Lobar Atrophy
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The Biology of Developmental Dyslexia
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Preclinical Detection of Parkinson's Disease
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The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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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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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Muscular Dystrophies
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Wilson Disease
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Neurological Management of Von Hippel-Lindau Disease
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Red Papules on the Tongue of a Patient with Hemiparesis
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Somatic Mutations in Cerebral Cortical Malformations
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Inherited Metabolic Diseases of the Nervous System, Galactosemia
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Inherited Metabolic Diseases of the Nervous System, Infantile Niemann-Pick Disease
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Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease)
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Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy
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Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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