Your browser doesn't support javascript.
loading
Phenotypic correlates and prognostic outcomes of TET2 mutations in myelodysplastic syndrome/myeloproliferative neoplasm overlap syndromes: A comprehensive study of 504 adult patients.
Coltro, Giacomo; Antelo, Guadalupe; Lasho, Terra L; Finke, Christy M; Pardanani, Animesh; Gangat, Naseema; Carr, Ryan M; Binder, Moritz; Mangaonkar, Abhishek A; Ketterling, Rhett; Fernandez-Zapico, Martin E; Robertson, Keith D; Bosi, Alberto; Vannucchi, Alessandro M; Tefferi, Ayalew; Patnaik, Mrinal M.
Afiliación
  • Coltro G; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Antelo G; Haematology Unit, Azienda Ospedaliero-Universitaria Careggi, Firenze, Italy.
  • Lasho TL; CRIMM, Centro di Ricerca e Innovazione per le Malattie Mieloproliferative, AOU Careggi, Firenze, Italy.
  • Finke CM; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Pardanani A; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Gangat N; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Carr RM; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Binder M; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Mangaonkar AA; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Ketterling R; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Fernandez-Zapico ME; Division of Hematology, Mayo Clinic, Rochester, Minnesota.
  • Robertson KD; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
  • Bosi A; Schulze Center for Novel Therapeutics, Division of Oncology Research, Mayo Clinic, Rochester, Minnesota.
  • Vannucchi AM; Schulze Center for Novel Therapeutics, Division of Oncology Research, Mayo Clinic, Rochester, Minnesota.
  • Tefferi A; Haematology Unit, Azienda Ospedaliero-Universitaria Careggi, Firenze, Italy.
  • Patnaik MM; Haematology Unit, Azienda Ospedaliero-Universitaria Careggi, Firenze, Italy.
Am J Hematol ; 95(4): E86-E89, 2020 04.
Article en En | MEDLINE | ID: mdl-31925810
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Mutación del Sistema de Lectura / Proteínas Proto-Oncogénicas / Codón sin Sentido / Proteínas de Unión al ADN / Estudios de Asociación Genética / Trastornos Mieloproliferativos / Proteínas de Neoplasias Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Humans / Infant / Male / Middle aged Idioma: En Revista: Am J Hematol Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Mutación del Sistema de Lectura / Proteínas Proto-Oncogénicas / Codón sin Sentido / Proteínas de Unión al ADN / Estudios de Asociación Genética / Trastornos Mieloproliferativos / Proteínas de Neoplasias Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Humans / Infant / Male / Middle aged Idioma: En Revista: Am J Hematol Año: 2020 Tipo del documento: Article