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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 6-Year-Old Girl with Progressive Toe Walking
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A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A Demure Teenager and Her Dystonic Foot
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Huntington Disease: Clinical Features and Diagnosis
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Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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Dopa-Responsive Dystonia Revisited
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MRI in Methylmalonic Acidemia
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Dopamine-Responsive Dystonia
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The DYT1 Phenotype and Guidelines for Diagnostic Testing
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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
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Dystonia and Chorea in Acquired Systemic Disorders
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Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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The Sit-up Test:An Alternative Clinical Test for Evaluating Pediatric Torticollis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
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Arteriovenous Malformation Presenting as Hemidystonia
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