Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia

• Raffaella Origa,
• Mario Cazzola,
• Elisabetta Mereu,
• Fabrice Danjou,
• Susanna Barella,
• Nicolina Giagu,
• Renzo Galanello,
• Dorine W. Swinkels

Affiliations

Raffaella Origa

Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy

Mario Cazzola

Department of Hematology Oncology, Fondazione IRCCS Policlinico San Matteo, and Department of Molecular Medicine, University of Pavia, Italy

Elisabetta Mereu

Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy

Fabrice Danjou

Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy

Susanna Barella

Ospedale Microcitemico-ASL 8, Cagliari, Italy

Nicolina Giagu

Ospedale Microcitemico-ASL 8, Cagliari, Italy

Renzo Galanello

Ospedale Microcitemico-Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Italy

Dorine W. Swinkels

Department of Laboratory Medicine, Radboud University medical center, Nijmegen, The Netherlands