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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…
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Keywords:
endothelial dysfunction;
hbe patients;
thalassemia hbe;
thalassemia ... See more keywords
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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…
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Keywords:
cell dysfunction;
hbe patients;
endothelial cell;
cell ... See more keywords
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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…
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Keywords:
hbe patients;
blood;
thalassaemia hbe;
study ... See more keywords