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

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Bibliographic Details
Published inHaematologica (Roma) Vol. 100; no. 5; pp. e169 - e171
Main Authors Origa, Raffaella, Cazzola, Mario, Mereu, Elisabetta, Danjou, Fabrice, Barella, Susanna, Giagu, Nicolina, Galanello, Renzo, Swinkels, Dorine W
Format Journal Article
LanguageEnglish
Published Italy Ferrata Storti Foundation 01.05.2015
Subjects
alpha-Thalassemia - blood
alpha-Thalassemia - diagnosis
alpha-Thalassemia - metabolism
beta-Thalassemia - blood
beta-Thalassemia - diagnosis
beta-Thalassemia - metabolism
Erythropoiesis
Growth Differentiation Factor 15 - blood
Growth Differentiation Factor 15 - metabolism
Hemolysis
Hepcidins - blood
Hepcidins - metabolism
Humans
Iron - metabolism
Iron Overload - metabolism
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hemoglobin H disease
β-thalassemia intermedia
erythropoiesis-hepcidin-iron store axis
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Bibliography:SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
Authors contributed equally
This work is dedicated to the memory and in honor of Renzo Galanello, who encouraged the study until the end of his career.
ISSN:0390-6078
1592-8721
DOI:10.3324/haematol.2014.115733