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

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Bibliographic Details
Published in:Haematologica (Roma) Vol. 100; no. 5; pp. e169 - e171
Main Authors: Origa, R., Cazzola, M., Mereu, E., Danjou, F., Barella, S., Giagu, N., Galanello, R., Swinkels, D. W.
Format: Journal Article
Language:English
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
ISSN:0390-6078, 1592-8721, 1592-8721
Online Access:Get full text
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Description
Bibliography:content type line 23
SourceType-Scholarly Journals-1
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
1592-8721
DOI:10.3324/haematol.2014.115733