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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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A Middle-Aged Man with Progressive Gait Abnormalities
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Neurodegeneration with Brain Iron Accumulation
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Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
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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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Degenerative Diseases of the Nervous System, Parkinson Disease
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A Pilot Study of Focused Ultrasound Thalamotomy for Essential Tremor
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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Evidence-based guideline update: Treatment of Essential Tremor
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Aicardi-Gouti�res Syndrome
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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A Genetic Risk Factor for Periodic Limb Movements in Sleep
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Deep Brain Stimulation
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GAMT Deficiency: Features, Treatment, and Outcome in an Inborn Error of Creatine Synthesis
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Therapies for Movement Disorders
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Niemann-Pick Disease Type C: Two Cases and an Update
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Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
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Diagnosis and Treatment of Wilson's Disease
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Tourette Syndrome:Update and Review of the Literature
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Cerebral Involvement in McLeod Syndrome
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The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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