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Mitochondrial DNA and Disease
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Paraneoplastic and Autoimmune Encephalitis
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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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A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
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Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
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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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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Progressive Supranuclear Palsy: A Current Review
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Posterior Cerebral Artery Syndromes
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Delayed Dystonia with Striatal CT Lucencies Induced by a Mycotoxin (3-Nitropropionic Acid)
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Acute Toxic Reaction to Carbamazepine:Clinical Effects and Serum Concentrations
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Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
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Diagnostic Tests for Choreoacanthocytosis
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Central Nervous System Germinomas, A Review
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Alternating Hemiplegia of Childhood
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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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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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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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Clinicopathologic Conference, LGI1 autoimmune encephalitis
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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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Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
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Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
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Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
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Basal Ganglia Involvement in Facio-Brachial Dystonic Seizures Associated with LGI1 Antibodies
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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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Rapidly Progressive Corticobasal Degeneration Syndrome
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Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
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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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Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
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