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The Genetic Landscape of Complex Childhood-Onset Hyperkinetic Movement Disorders.
Pérez-Dueñas, Belén; Gorman, Kathleen; Marcé-Grau, Anna; Ortigoza-Escobar, Juan D; Macaya, Alfons; Danti, Federica R; Barwick, Katy; Papandreou, Apostolos; Ng, Joanne; Meyer, Esther; Mohammad, Shekeeb S; Smith, Martin; Muntoni, Francesco; Munot, Pinki; Uusimaa, Johanna; Vieira, Päivi; Sheridan, Eammon; Guerrini, Renzo; Cobben, Jan; Yilmaz, Sanem; De Grandis, Elisa; Dale, Russell C; Pons, Roser; Peall, Kathryn J; Leuzzi, Vincenzo; Kurian, Manju A.
Afiliación
  • Pérez-Dueñas B; Department of Pediatric Neurology, Vall d'Hebron Hospital Universitary and Vall d'Hebrón Research Institute (VHIR)., Barcelona, Spain.
  • Gorman K; Department of Pediatrics, Obstetrics, Gynecology, Preventative Medicine and Public Health, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Marcé-Grau A; Center for Biomedical Network Research on Rare Diseases (CIBERER) CB06/07/0063, Barcelona, Spain.
  • Ortigoza-Escobar JD; Developmental Neurosciences Programme, Great Ormond Street-Institute of Child Health, University College London, London, United Kingdom.
  • Macaya A; Dubowitz neuromuscular Center, Great Ormond Street Hospital for Children, London, United Kingdom.
  • Danti FR; Department of Pediatric Neurology, Vall d'Hebron Hospital Universitary and Vall d'Hebrón Research Institute (VHIR)., Barcelona, Spain.
  • Barwick K; Department of Pediatric Neurology, Sant Joan de Déu Hospital, Barcelona, Spain.
  • Papandreou A; Department of Pediatric Neurology, Vall d'Hebron Hospital Universitary and Vall d'Hebrón Research Institute (VHIR)., Barcelona, Spain.
  • Ng J; Department of Pediatrics, Obstetrics, Gynecology, Preventative Medicine and Public Health, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Meyer E; Center for Biomedical Network Research on Rare Diseases (CIBERER) CB06/07/0063, Barcelona, Spain.
  • Mohammad SS; Unit of Child Neurology and Psychiatry, Department of Human Neuroscience, Sapienza University of Rome, Rome, Italy.
  • Smith M; Developmental Neurosciences Programme, Great Ormond Street-Institute of Child Health, University College London, London, United Kingdom.
  • Muntoni F; Developmental Neurosciences Programme, Great Ormond Street-Institute of Child Health, University College London, London, United Kingdom.
  • Munot P; Dubowitz neuromuscular Center, Great Ormond Street Hospital for Children, London, United Kingdom.
  • Uusimaa J; Gene Transfer Technology Group, Institute for Women's Health, University College London, London, United Kingdom.
  • Vieira P; Developmental Neurosciences Programme, Great Ormond Street-Institute of Child Health, University College London, London, United Kingdom.
  • Sheridan E; Kids Neuroscience Centre and Brain and Mind Centre, Faculty of Medicine and Health, University of Sydney, Westmead, New South Wales, Australia.
  • Guerrini R; Department of Pediatric Neurology, John Radcliffe Hospital, Oxford, United Kingdom.
  • Cobben J; Developmental Neurosciences Programme, Great Ormond Street-Institute of Child Health, University College London, London, United Kingdom.
  • Yilmaz S; Dubowitz neuromuscular Center, Great Ormond Street Hospital for Children, London, United Kingdom.
  • De Grandis E; Dubowitz neuromuscular Center, Great Ormond Street Hospital for Children, London, United Kingdom.
  • Dale RC; PEDEGO Research Unit, Department of Children and Adolescents, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Oulu, Finland.
  • Pons R; PEDEGO Research Unit, Department of Children and Adolescents, Medical Research Center Oulu, Oulu University Hospital, University of Oulu, Oulu, Finland.
  • Peall KJ; School of Medicine, St James's University Hospital, University of Leeds, Leeds, United Kingdom.
  • Leuzzi V; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Neuroscience Department, A. Meyer Children's Hospital, University of Florence, Florence, Italy.
  • Kurian MA; North West Thames Regional Genetic Service, Northwick Park Hospital, London, United Kingdom.
Mov Disord ; 37(11): 2197-2209, 2022 11.
Article en En | MEDLINE | ID: mdl-36054588
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Texto completo: 1 Colección: 01-internacional Asunto principal: Corea / Trastornos Distónicos / Distonía / Trastornos del Movimiento Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Child / Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: España
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Texto completo: 1 Colección: 01-internacional Asunto principal: Corea / Trastornos Distónicos / Distonía / Trastornos del Movimiento Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Child / Humans Idioma: En Revista: Mov Disord Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: España