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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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Mitochondrial DNA and Disease
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Extrapyramidal Involvement in Rett's Syndrome
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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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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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
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Functional Gait Disorders
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A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
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Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019
Pyruvate Dehydrogenase Deficiency (PDCD)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017
Huntington Disease: Clinical Features and Diagnosis
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A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
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Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
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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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Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
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Rapidly Progressive Corticobasal Degeneration Syndrome
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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Progressive Supranuclear Palsy: A Current Review
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Dopamine-Responsive Dystonia
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Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004
Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000
Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000
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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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998
Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
Neurol 48:376-380, Louis,E.D.,et al, 1997
Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996
Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996
Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
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