Functional Movement Disorders in Children von Chouksey, Anjali, Pandey, Sanjay

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Prominent jaw closure dystonia, awake bruxism, and stereotypies in a patient with hypoglycemic encephalopathy von Vijayaraghavan, Asish, Chouksey, Anjali

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A clinical approach to the patients with combination of dystonia and myoclonus von Anjali Chouksey, Sanjay Pandey

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Functional Movement Disorders in Elderly von Chouksey, Anjali, Pandey, Sanjay

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Phenotypic variability in huntington's disease von Chouksey, Anjali, Pandey, Sanjay

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Huntington’s disease—not just a disease of brain but mind as well von Anjali Chouksey, Sanjay Pandey

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ATP1A3 mutation presenting as CAPOS syndrome plus dystonia phenotype von Chouksey, Anjali, Pandey, Sanjay

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Autoimmune Movement Disorders: A Video-Based Case Series of 11 Patients von Chouksey, Anjali, Pandey, Sanjay

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ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype von Chouksey, Anjali, Pandey, Sanjay

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Clinical Spectrum of Drug-Induced Movement Disorders: A Study of 97 Patients von Chouksey, Anjali, Pandey, Sanjay

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Dancing Dorsal Quadrilaterals—Organic or Functional? von Chouksey, Anjali, Pandey, Sanjay, Hallett, Mark

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Gender Differences in Functional Movement Disorder: Sociocultural or Biological? von Chouksey, Anjali, Pandey, Sanjay

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Reply - Clinical Spectrum of Drug-Induced Movement Disorders: A Study of 97 Patients von Chouksey, Anjali, Pandey, Sanjay

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The multiple twists in the tale: Brain iron accumulation, facial jerks, and truncal dystonia von Chouksey, Anjali, Mohan, Sony, Aaron, Rekha, Mathew, Vivek

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Poststroke movement disorders: One etiology many phenotypes von Chouksey, Anjali, Pandey, Sanjay

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Functional Movement Disorders in Elderly von Chouksey, Anjali, Pandey, Sanjay

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Severe Choreo‐Ballism Episodes Due to PRRT2 Gene Mutations—A Vignette von Pandey, Sanjay, Chouksey, Anjali, Bhattad, Sonali

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Movement Disorders and Musculoskeletal System: A Reciprocal Relationship von Pandey, Sanjay, Chouksey, Anjali, Pitakpatapee, Yuvadee, Srivanitchapoom, Prachaya

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Long‐Term Follow‐Up of a Patient with a De Novo p. Arg769Cys Mutation in the ATP1A3 Gene von Chouksey, Anjali, Vijayaraghavan, Asish, Mohan, Sony, Inturi, Srija, Prabhakar, A.T., Mathew, Vivek

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Long‐Term Follow‐Up of a Patient with a De Novo p.Arg769Cys Mutation in the ATP1A3 Gene von Chouksey, Anjali, Vijayaraghavan, Asish, Mohan, Sony, Inturi, Srija, Prabhakar, A.T., Mathew, Vivek

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