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Understanding barriers to diagnosis in a rare, genetic disease: Delays and errors in diagnosing schwannomatosis.
Merker, Vanessa L; Slobogean, Bronwyn; Jordan, Justin T; Langmead, Shannon; Meterko, Mark; Charns, Martin P; Elwy, A Rani; Blakeley, Jaishri O; Plotkin, Scott R.
Afiliação
  • Merker VL; Department of Neurology and Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Slobogean B; Department of Neurology and Neurosurgery, Johns Hopkins University, Baltimore, Maryland, USA.
  • Jordan JT; Department of Neurology and Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Langmead S; Department of Neurology and Neurosurgery, Johns Hopkins University, Baltimore, Maryland, USA.
  • Meterko M; Analytics and Performance Integration, Office of Quality and Patient Safety, Veterans Health Administration, Bedford, Massachusetts, USA.
  • Charns MP; Department of Health Law, Policy and Management, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Elwy AR; Department of Health Law, Policy and Management, Boston University School of Public Health, Boston, Massachusetts, USA.
  • Blakeley JO; Center for Healthcare Organization and Implementation Research (CHOIR), VA Boston Healthcare System, Boston, Massachusetts, USA.
  • Plotkin SR; Center for Healthcare Organization and Implementation Research (CHOIR), VA Bedford Healthcare System, Bedford, Massachusetts, USA.
Am J Med Genet A ; 188(9): 2672-2683, 2022 09.
Article em En | MEDLINE | ID: mdl-35678462

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neurofibromatose 2 / Neurofibromatoses / Neurilemoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neurofibromatose 2 / Neurofibromatoses / Neurilemoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article