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The Phenotypic Continuum of ATP1A3-Related Disorders
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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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Neurodegeneration with Brain Iron Accumulation
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Antibody-Mediated Encephalitis
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Clinical Manifestations of the anti-IgLON5 Disease
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Paraneoplastic and Autoimmune Encephalitis
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Huntington Disease: Clinical Features and Diagnosis
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Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
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MRI in Methylmalonic Acidemia
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Sydenham's Chorea:Physical and Psychological Symptoms of St. Vitus Dance
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Neurologic Sequelae of Open-Heart Surgery in Children
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Chronic Progressive Panencephalitis due to Rubella Virus Simulating Subacute Sclerosing Panencephalitis
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Delayed-Onset MRI Findings in Acute Chorea Related to Anoxic Brain Injury
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Recombinant Interferon-a-induced Chorea and Frontal Subcortical Dementia
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Delayed Movement Disorders After Carbon Monoxide Poisoning
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Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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Reversible Dementia and Chorea in a Young Woman with the Lupus Anticoagulant
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Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
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Wilson's Disease:The Problem of Delayed Diagnosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Huntington Disease Associated with Alzheimer Disease
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Familial Idiopathic Cerebral Calcifications
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Neurologic Disorders in Renal Failure (1st of Two Parts)
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Normocalcemic Tetany
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Progressive Rubella Encephalitis
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