about
Laboratory use of hepcidin in renal transplant recipientsEffect of breastfeeding versus infant formula on iron status of infants with beta thalassemia major.Inadequate dietary intake in patients with thalassemiaPrevalence of glutathione S-transferase gene deletions and their effect on sickle cell patients.Erythropoietic drive is the strongest predictor of hepcidin level in adults with sickle cell diseaseJoint Model of Iron and Hepcidin During the Menstrual Cycle in Healthy WomenCombined therapy of iron chelator and antioxidant completely restores brain dysfunction induced by iron toxicity.Iron overload in Beta thalassaemia major and intermedia patients.New strategies to target iron metabolism for the treatment of beta thalassemia
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Iron metabolism in thalassemia and sickle cell disease
@ast
Iron metabolism in thalassemia and sickle cell disease
@en
Iron metabolism in thalassemia and sickle cell disease
@nl
type
label
Iron metabolism in thalassemia and sickle cell disease
@ast
Iron metabolism in thalassemia and sickle cell disease
@en
Iron metabolism in thalassemia and sickle cell disease
@nl
prefLabel
Iron metabolism in thalassemia and sickle cell disease
@ast
Iron metabolism in thalassemia and sickle cell disease
@en
Iron metabolism in thalassemia and sickle cell disease
@nl
P2093
P2860
P356
P1476
Iron metabolism in thalassemia and sickle cell disease
@en
P2093
Alberto Piperno
Matteo Pozzi
Paola Trombini
Raffaella Mariani
P2860
P304
P356
10.4084/MJHID.2009.006
P577
2009-10-27T00:00:00Z