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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Detaylı Bibliyografya
Yayımlandı:Br J Haematol
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2020
Konular:
Article
Online Erişim: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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