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A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
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Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
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Aicardi-Gouti�res Syndrome
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Mitochondrial DNA and Disease
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Pseudochoreoatheotosis:Movement Associated with Loss of Proprioception
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024
The Phenotypic Continuum of ATP1A3-Related Disorders
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Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021
Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
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Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
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MRI in Methylmalonic Acidemia
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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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Post-Streptococcal Autoimmune Disorders of the Central Nervous System
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Cervical Disc Prolapse with Cord Compression Presenting with Choreoathetosis and Dystonia
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Delayed Dystonia with Striatal CT Lucencies Induced by a Mycotoxin (3-Nitropropionic Acid)
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Wilson Disease
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Cervical Dystonia:Clinical Findings and Associated Movement Disorders
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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A 6-Year-Old Girl with Progressive Toe Walking
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A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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Paraneoplastic and Autoimmune Encephalitis
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Huntington Disease: Clinical Features and Diagnosis
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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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Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
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Huntingtons Disease
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N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
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TENS for the Treatment of Writers Cramp Dystonia:A Randomized, Placebo-Controlled Study
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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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Dystonia and Chorea in Acquired Systemic Disorders
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Posterior Cerebral Artery Syndromes
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Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
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Tremor and Other Movement Disorders after Whiplash Type Injuries
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Thalamic Tremor:Case Reports and Implications of the Tremor-Generating Mechanism
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Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
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Striatopallidal and Thalamic Dystonia, A Magnetic Resonance Imaging Anatomoclinical Study
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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