Hepcidin and β-thalassemia major
Author:
Affiliation:
1. UNIVERSITY OF CALIFORNIA, LOS ANGELES
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/122/1/3/1369075/3.pdf
Reference9 articles.
1. Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with beta-thalassemia major: a longitudinal study.;Pasricha;Blood,2013
2. Treating iron overload in patients with non-transfusion-dependent thalassemia.;Taher;Am J Hematol,2013
3. Hepcidin in iron overload disorders.;Papanikolaou;Blood,2005
4. Urinary hepcidin in congenital chronic anemias.;Kearney;Pediatr Blood Cancer,2007
5. Liver iron concentrations and urinary hepcidin in beta-thalassemia.;Origa;Haematologica,2007
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2. Study of growth differentiation factor-15 in polytransfused children with β-thalassemia;Indian Journal of Pathology and Microbiology;2023
3. Iron Deficiency Anemia;Reference Module in Biomedical Sciences;2023
4. The effect of erythroferrone suppression by transfusion on the erythropoietin–erythroferrone–hepcidin axis in transfusion‐dependent thalassaemia: A pre–post cohort study;British Journal of Haematology;2022-12-19
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