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Acquired Neurosyphilis Presenting as Movement Disorders
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Myoclonus Secondary to Albuterol (Salbutamol) instillation
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Delayed Movement Disorders After Carbon Monoxide Poisoning
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Myoclonus Associated with Propafenone
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Drug Induced Creutzfeldt-Jakob Like Syndrome
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Multistate Outbreak of Poisonings Associated with Illicit Use of Gamma Hydroxy Butyrate
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Extrapyramidal Involvement in Rett's Syndrome
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Hypoxic-Ischemic Damage of the Basal Ganglia
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Myoclonus Induced by Metoclopramide Therapy
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Persisting Neurologic Sequelae of Lithium Carbonate Therapy
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Meperidine-Associated Myoclonus & Seizures in Long-Term Hemodialysis Patients
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Neurologic Disorders in Renal Failure (1st of Two Parts)
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A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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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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Clinicopathologic Conference, Borrelia Miyamotoi Infection
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
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Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
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Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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A Case of Altered Mental Status, Not Otherwise Specified
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A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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The Eye of the Beholder: Inter-rater Agreement among Experts on Psychogenic Jerky Movement Disorders
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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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Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
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Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
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Whipples Disease
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Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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