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

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Podrobná bibliografia
Vydané v:	Haematologica (Roma) Ročník 100; číslo 5; s. e169 - e171
Hlavní autori:	Origa, R., Cazzola, M., Mereu, E., Danjou, F., Barella, S., Giagu, N., Galanello, R., Swinkels, D. W.
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Italy Ferrata Storti Foundation 01.05.2015
Predmet:	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 Online Only hemoglobin H disease β-thalassemia intermedia erythropoiesis-hepcidin-iron store axis
ISSN:	0390-6078, 1592-8721, 1592-8721
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Popis
Bibliografia:	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