Regulation of iron homeostasis through the erythroferrone-hepcidin axis in sickle cell disease

Sickle cell disease (SCD) has a distinct pattern of transfusional iron overload (IO) when compared to transfusion-dependent β-thalassaemia major (TDT). We conducted a single institution prospective study to evaluate plasma biomarkers of iron regulation and inflammation in patients with SCD with IO (...

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Bibliographic Details
Published in:Br J Haematol
Main Authors: Mangaonkar, Abhishek A., Thawer, Fahim, Son, James, Ajebo, Germame, Xu, Hongyan, Barrett, Nadine J., Wells, Leigh G., Bowman, Latanya, Clair, Betsy, Patel, Niren, Bora, Pritam, Jung, Grace, Nemeth, Elizabeta, Kutlar, Abdullah
Format: Artigo
Language:Inglês
Published: 2020
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC8011855/
https://ncbi.nlm.nih.gov/pubmed/32030737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjh.16498
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