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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發表在: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
格式: Artigo
語言:Inglês
出版: 2020
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Article
在線閱讀: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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