The Phenotypic Continuum of ATP1A3-Related Disorders
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Huntington Disease: Clinical Features and Diagnosis
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Sjogren Syndrome: Neurologic Complications
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Aicardi-Gouti�res Syndrome
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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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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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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Current and Emerging Issues in Wilsons Disease
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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 Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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MR Imaging of the Brain in Neurologic Wilson Disease
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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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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Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
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Paroxysmal Kinesigenic Dyskinesia
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Deep-Brain Stimulation - Entering the Era of Human Neural-Network Modulation
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Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
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Criteria for the Diagnosis of Corticobasal Degeneration
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Parkin Disease
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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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Dopa-Responsive Dystonia Revisited
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Deep Brain Stimulation
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Rapidly Progressive Corticobasal Degeneration Syndrome
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