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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Current and Emerging Issues in Wilsons Disease
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Torticollis in a Child with Otalgia
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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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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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Functional Gait Disorders
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A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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Neurodegeneration with Brain Iron Accumulation
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Paraneoplastic and Autoimmune Encephalitis
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Huntington Disease: Clinical Features and Diagnosis
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
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Criteria for the Diagnosis of Corticobasal Degeneration
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Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
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Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
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Dopa-Responsive Dystonia Revisited
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Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Sjogren Syndrome: Neurologic Complications
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Aicardi-Gouti�res Syndrome
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Progressive Supranuclear Palsy: A Current Review
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Long-term Outcome of Bilateal Pallidal Deep Brain Stimulation for Primary Cervical Dystonia
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Long-Term Outcome of Bilateral Pallidal Deep Brain Stimulation for Primary Cervical Dystonia
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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Deep Brain Stimulation
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Secondary Motor Disturbances in 101 Patients With Musicians Dystonia
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Post-Stroke Movement Disorders; Report of 56 Patients
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Diagnostic Criteria for Dystonia in DYT1 Families
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The DYT1 Phenotype and Guidelines for Diagnostic Testing
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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