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Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and ß-thalassemia intermedia.
Origa, Raffaella; Cazzola, Mario; Mereu, Elisabetta; Danjou, Fabrice; Barella, Susanna; Giagu, Nicolina; Galanello, Renzo; Swinkels, Dorine W.
Afiliación
  • Origa R; Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy.
  • Cazzola M; Department of Hematology Oncology, Fondazione IRCCS Policlinico San Matteo, and Department of Molecular Medicine, University of Pavia, Italy.
  • Mereu E; Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy.
  • Danjou F; Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy.
  • Barella S; Ospedale Microcitemico-ASL 8, Cagliari, Italy.
  • Giagu N; Ospedale Microcitemico-ASL 8, Cagliari, Italy.
  • Galanello R; Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy.
  • Swinkels DW; Department of Laboratory Medicine, Radboud University medical center, Nijmegen, The Netherlands Dorine.Swinkels@Radboudumc.nl.
Haematologica ; 100(5): e169-71, 2015 May.
Article en En | MEDLINE | ID: mdl-25596269
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Talasemia beta / Talasemia alfa / Eritropoyesis / Hepcidinas / Hierro Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Haematologica Año: 2015 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Talasemia beta / Talasemia alfa / Eritropoyesis / Hepcidinas / Hierro Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Haematologica Año: 2015 Tipo del documento: Article País de afiliación: Italia