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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Cortical Myoclonus in Huntington's Disease
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Myoclonus in Adult Huntington's Disease
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Familial Chorea & Myoclonus Epilepsy
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Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
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Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
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Antibody-Mediated Encephalitis
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Neuroimaging Changes in Menkes Disease, Part 1
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Rapidly Progressive Quadriplegia and Encephalopathy
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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A 27-Year Old Man with Rapidly Progressive Coma
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Subacute Sclerosing Panencephalitis
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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Progressive Gait Deterioration in Adolescents with Dravet Syndrome
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Acquired Neurosyphilis Presenting as Movement Disorders
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
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Whipples Disease
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Post-Stroke Movement Disorders; Report of 56 Patients
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
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N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
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Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
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Delayed Movement Disorders After Carbon Monoxide Poisoning
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Creutzfeldt-Jakob Disease in a Young Woman
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Mitochondrial DNA and Disease
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
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Familial Alzheimer's Disease
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
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Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
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