Liver iron concentrations and urinary hepcidin in beta-thalassemia.
about
Beta-thalassemiaIneffective erythropoiesis and thalassemiasThe liver-specific microRNA miR-122 controls systemic iron homeostasis in miceMolecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesisHepcidin in the diagnosis of iron disordersProfile of deferasirox for the treatment of patients with non-transfusion-dependent thalassemia syndromesβ-thalassemia intermedia: a clinical perspectiveHepcidin and iron homeostasisNew insights into iron regulation and erythropoiesisTreating iron overload in patients with non-transfusion-dependent thalassemiaModulation of hepcidin as therapy for primary and secondary iron overload disorders: preclinical models and approachesOutward- and inward-facing structures of a putative bacterial transition-metal transporter with homology to ferroportin.Hepcidin and iron regulation, 10 years later.Iron homeostasis in host defence and inflammationβ-thalassemias: paradigmatic diseases for scientific discoveries and development of innovative therapiesIdentification of erythroferrone as an erythroid regulator of iron metabolismDecision points in the treatment of transfusional iron overload in patients with myelodysplastic syndromes: why, when, and how to chelate.Advances in quantitative hepcidin measurements by time-of-flight mass spectrometryAn insight into the relationships between hepcidin, anemia, infections and inflammatory cytokines in pediatric refugees: a cross-sectional study.Hydroxyurea for reducing blood transfusion in non-transfusion dependent beta thalassaemias.Targeting the hepcidin-ferroportin axis in the diagnosis and treatment of anemiasDual-energy X-ray absorptiometry with serum ferritin predicts liver iron concentration and changes in concentration better than ferritin alone.Future alternative therapies for β-thalassemia.Biopsy-based calibration of T2* magnetic resonance for estimation of liver iron concentration and comparison with R2 Ferriscan.Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependencyIron overload in sickle cell disease.Contribution of STAT3 and SMAD4 pathways to the regulation of hepcidin by opposing stimuli.Molecular liaisons between erythropoiesis and iron metabolismMolecular mechanisms of hepcidin regulation: implications for the anemia of CKD.Spleen R2 and R2* in iron-overloaded patients with sickle cell disease and thalassemia major.Hepcidin in beta-thalassemia.Iron overload cardiomyopathy: better understanding of an increasing disorder.Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I.Splenectomy improves anaemia but does not reduce iron burden in patients with haemoglobin H Constant Spring disease.Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of β-thalassemia.Iron metabolism in thalassemia and sickle cell diseaseThalassaemia intermedia: an update.Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.Endocrine and bone complications in β-thalassemia intermedia: current understanding and treatmentAltered erythropoiesis and iron metabolism in carriers of thalassemia
P2860
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P2860
Liver iron concentrations and urinary hepcidin in beta-thalassemia.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Liver iron concentrations and urinary hepcidin in beta-thalassemia.
@en
type
label
Liver iron concentrations and urinary hepcidin in beta-thalassemia.
@en
prefLabel
Liver iron concentrations and urinary hepcidin in beta-thalassemia.
@en
P2093
P50
P356
P1433
P1476
Liver iron concentrations and urinary hepcidin in beta-thalassemia.
@en
P2093
Elizabeta Nemeth
Liliana Maccioni
Nicolina Giagu
Renzo Galanello
P304
P356
10.3324/HAEMATOL.10842
P577
2007-05-01T00:00:00Z