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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Rapidly Progressive Corticobasal Degeneration Syndrome
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Cortical-Basal Ganglionic Degeneration
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
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Adults with Cerebral Palsy Require Ongoing Neurologic Care
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
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A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
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A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
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Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Post-Stroke Movement Disorders; Report of 56 Patients
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Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
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Pseudochoreoatheotosis:Movement Associated with Loss of Proprioception
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Diagnostic Tests for Choreoacanthocytosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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The Movement Disorder of Reflex Sympathetic Dystrophy
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