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A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
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Post-Streptococcal Autoimmune Dystonia With Isolated Bilateral Striatal Necrosis
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Hemidystonia Due to a Contralateral Parietooccipital Metastasis:Disappearance after Removal of the Mass Lesion
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Central Nervous System Germinomas, A Review
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
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Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Lithium-Induced Reversible Pisa Syndrome
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Paraneoplastic and Autoimmune Encephalitis
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Huntington Disease: Clinical Features and Diagnosis
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Practice Guideline Update Summary: Botulinum Neurotoxin for the Treatment of Blepharospasm, Cervical Dystonia, Adult Spasticity, and Headache
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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Myasthenia Gravis after Botulinum Toxin Type A Injection
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
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Criteria for the Diagnosis of Corticobasal Degeneration
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Delayed Onset of Progressive Chorea After Acute Basal Ganglia Injury
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Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Aicardi-Gouti�res Syndrome
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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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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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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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Acute Dystonic Reactions to "Street Xanax"
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HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
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