Current and Emerging Issues in Wilsons Disease
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Aicardi-Gouti�res Syndrome
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Niemann-Pick Disease Type C: Two Cases and an Update
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Niemann-Pick Disease Type C from Bench to Bedside
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Wilson Disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Corticodentatonigral Degeneration with Neuronal Achromasia
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
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The Phenotypic Continuum of ATP1A3-Related Disorders
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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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Functional Gait Disorders
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Neurodegeneration with Brain Iron Accumulation
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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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
NEJM 377:2376-2385, Case 38-2017, 2017
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, The Phenylketonuria
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Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
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Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
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Criteria for the Diagnosis of Corticobasal Degeneration
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Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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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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Autoimmune encephalitis
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MRI in Methylmalonic Acidemia
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable 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
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010
Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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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
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008
Pallidal Deep-Brain Stimulation in Primary Generalized or Segmental Dystonia
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Mental Retardation
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Therapies for Movement Disorders
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Blepharospasm
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Drug-Induced Pisa Syndrome (Pleurothotomus)
CNS Drugs 10:166-174, Suzuki, T. & Matsuzaka, H., 2002
Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000
Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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