Abnormal red blood cell morphological changes in thalassaemia associated with iron overload and oxidative stress

AimsIron overload is a major factor contributing to the overall pathology of thalassaemia, which is primarily mediated by ineffective erythropoiesis and shorter mature red blood cell (RBC) survival. Iron accumulation in RBCs generates reactive oxygen species (ROS) that cause cellular damage such as...

Full description

Saved in:
Bibliographic Details
Published inJournal of clinical pathology Vol. 72; no. 8; pp. 520 - 524
Main Authors Chaichompoo, Pornthip, Qillah, Ariz, Sirankapracha, Pornpan, Kaewchuchuen, Jirada, Rimthong, Poramate, Paiboonsukwong, Kittiphong, Fucharoen, Suthat, Svasti, Saovaros, Worawichawong, Suchin
Format Journal Article
LanguageEnglish
Published England BMJ Publishing Group LTD 01.08.2019
Subjects
Online AccessGet full text

Cover

Loading…