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Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients.
Saliba, Antoine N; Ferrer, Alejandro; Gangat, Naseema; Pruthi, Rajiv K; Tefferi, Ayalew; Higgins, Alexandra; Bezerra, Evandro D; Buglioni, Alessia; Salama, Mohamed E; Klee, Eric W; Pinto E Vairo, Filippo; Mangaonkar, Abhishek; Majerus, Julie; Chen, Dong; Patnaik, Mrinal M.
Afiliação
  • Saliba AN; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Ferrer A; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Gangat N; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Pruthi RK; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Tefferi A; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Higgins A; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Bezerra ED; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Buglioni A; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Salama ME; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Klee EW; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Pinto E Vairo F; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Mangaonkar A; Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
  • Majerus J; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Chen D; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Patnaik MM; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Br J Haematol ; 190(5): e316-e320, 2020 09.
Article em En | MEDLINE | ID: mdl-32567678
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Plaquetários / Proteínas Sanguíneas / Mutação de Sentido Incorreto / Mielofibrose Primária / Doenças Genéticas Inatas Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Plaquetários / Proteínas Sanguíneas / Mutação de Sentido Incorreto / Mielofibrose Primária / Doenças Genéticas Inatas Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article