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A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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Huntington Disease: Clinical Features and Diagnosis
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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Mitochondrial DNA and Disease
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Current and Emerging Issues in Wilsons Disease
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A 6-Year-Old Girl with Progressive Toe Walking
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A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
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Adults with Cerebral Palsy Require Ongoing Neurologic Care
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Functional Gait Disorders
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Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Pyruvate Dehydrogenase Deficiency (PDCD)
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A Demure Teenager and Her Dystonic Foot
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Paraneoplastic and Autoimmune Encephalitis
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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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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A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
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Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
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Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
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Rapidly Progressive Corticobasal Degeneration Syndrome
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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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Pneumonias Link With the Head and Neck
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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Dopamine-Responsive Dystonia
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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