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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
Jabbari, Edwin; Koga, Shunsuke; Valentino, Rebecca R; Reynolds, Regina H; Ferrari, Raffaele; Tan, Manuela M X; Rowe, James B; Dalgard, Clifton L; Scholz, Sonja W; Dickson, Dennis W; Warner, Thomas T; Revesz, Tamas; Höglinger, Günter U; Ross, Owen A; Ryten, Mina; Hardy, John; Shoai, Maryam; Morris, Huw R.
Afiliação
  • Jabbari E; Department of Clinical and Movement Neurosciences, University College London Queen Square Institute of Neurology, London, UK; Movement Disorders Centre, University College London Queen Square Institute of Neurology, London, UK. Electronic address: e.jabbari@ucl.ac.uk.
  • Koga S; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Valentino RR; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Reynolds RH; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK; NIHR Great Ormond Street Hospital Biomedical Research Centre, University College London, London, UK; Great Ormond Street Institute of Child Health, Genetics and Genomic Medicine, Unive
  • Ferrari R; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK.
  • Tan MMX; Department of Clinical and Movement Neurosciences, University College London Queen Square Institute of Neurology, London, UK; Movement Disorders Centre, University College London Queen Square Institute of Neurology, London, UK.
  • Rowe JB; Department of Clinical Neurosciences, University of Cambridge, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Dalgard CL; Department of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
  • Scholz SW; Department of Neurology, Johns Hopkins University Medical Center, Baltimore, MD, USA; Neurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Dickson DW; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Warner TT; Reta Lila Weston Institute, University College London Queen Square Institute of Neurology, London, UK; Queen Square Brain Bank for Neurological Disorders, University College London Queen Square Institute of Neurology, London, UK.
  • Revesz T; Reta Lila Weston Institute, University College London Queen Square Institute of Neurology, London, UK; Queen Square Brain Bank for Neurological Disorders, University College London Queen Square Institute of Neurology, London, UK.
  • Höglinger GU; German Center for Neurodegenerative Diseases, Munich, Germany; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Ross OA; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Ryten M; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK; NIHR Great Ormond Street Hospital Biomedical Research Centre, University College London, London, UK; Great Ormond Street Institute of Child Health, Genetics and Genomic Medicine, Unive
  • Hardy J; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK; Reta Lila Weston Institute, University College London Queen Square Institute of Neurology, London, UK; Dementia Research Institute at University College London, University College Lond
  • Shoai M; Department of Neurodegenerative Disease, University College London Queen Square Institute of Neurology, London, UK.
  • Morris HR; Department of Clinical and Movement Neurosciences, University College London Queen Square Institute of Neurology, London, UK; Movement Disorders Centre, University College London Queen Square Institute of Neurology, London, UK. Electronic address: h.morris@ucl.ac.uk.
Lancet Neurol ; 20(2): 107-116, 2021 02.
Article em En | MEDLINE | ID: mdl-33341150
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Estudo de Associação Genômica Ampla Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Estudo de Associação Genômica Ampla Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Neurol Assunto da revista: NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article