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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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Aicardi-Gouti�res Syndrome
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995
Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Cortical-Basal Ganglionic Degeneration
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Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
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Corticodentatonigral Degeneration with Neuronal Achromasia
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A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017
Huntington Disease: Clinical Features and Diagnosis
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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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Huntingtons Disease
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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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Progressive Supranuclear Palsy: A Current Review
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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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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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Niemann-Pick Disease Type C from Bench to Bedside
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Diagnostic Tests for Choreoacanthocytosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Central Nervous System Germinomas, A Review
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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Progressive Supranuclear Palsy-Case Study
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021
Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
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A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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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
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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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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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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Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
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Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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