Articles with "hbe patients" as a keyword



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Depleted nitric oxide and prostaglandin E2 levels are correlated with endothelial dysfunction in β-thalassemia/HbE patients

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Published in 2017 at "International Journal of Hematology"

DOI: 10.1007/s12185-017-2247-8

Abstract: Mechanisms of vascular disorders in β-thalassemia/HbE patients remain poorly understood. In the present study, we aimed to determine the presence of endothelial dysfunction and its association with altered vascular mediators in this population. Forty-three β-thalassemia/HbE… read more here.

Keywords: endothelial dysfunction; hbe patients; thalassemia hbe; thalassemia ... See more keywords
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Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction

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Published in 2018 at "Scientific Reports"

DOI: 10.1038/s41598-018-31386-6

Abstract: Thromboembolic complication occurs frequently in β-thalassaemia/HbE patients, particularly in splenectomised patients. Endothelial cells play an important role in thrombosis. There is strong evidence of endothelial cell activation and dysfunction in β-thalassaemia. Microparticles (MPs) are associated… read more here.

Keywords: cell dysfunction; hbe patients; endothelial cell; cell ... See more keywords
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A comprehensive study of immune function and immunophenotyping of white blood cells from β‐thalassaemia/HbE patients on hydroxyurea supports the safety of the drug

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Published in 2022 at "British Journal of Haematology"

DOI: 10.1111/bjh.18508

Abstract: Hydroxyurea (HU) (hydroxycarbamide) is used as a therapeutic option in β‐thalassaemia to increase fetal haemoglobin, which results in a reduced requirement for blood transfusion. However, a potential serious adverse effect of HU is neutropenia. Abnormal… read more here.

Keywords: hbe patients; blood; thalassaemia hbe; study ... See more keywords