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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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| Published in: | Br J Haematol |
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| Main Authors: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
2020
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| Subjects: | |
| 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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