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Movement Disorders with Cerebral Toxoplasmosis and AIDS
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Movement Disorders & AIDS
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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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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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
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Neurodegeneration with Brain Iron Accumulation
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
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Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
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Pyruvate Dehydrogenase Deficiency (PDCD)
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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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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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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
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Criteria for the Diagnosis of Corticobasal Degeneration
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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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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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Sjogren Syndrome: Neurologic Complications
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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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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
Brain 130:2484-2493, Jen, J.C.,et al, 2007
Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006
Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
Ann Neurol 57:738-741,613, Castelnau,P.,et al, 2005
Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004
Uses of Botulinum Toxin Injection in Medicine Today
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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
Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999
Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999
Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998
Post-Traumatic Shoulder 'Dystonia':Persistent Abnormal Postures of the Shoulder After Minor Trauma
Neurol 51:1205-1207, Thyagarajan,D.,et al, 1998
Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
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