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pubmed-article:18456387pubmed:abstractTextbeta-thalassemia major, or Cooley's anemia, is a red blood cell disorder requiring lifelong blood transfusions for survival. Erythrocytes accumulate toxic iron at their membranes, triggering an oxidative cascade that leads to their premature destruction in high numbers. We hypothesized that removing this proximate iron compartment as a primary treatment, using standard and alternative orally active iron chelators, could prevent hastened red cell removal and, clinically, perhaps alleviate the need for transfusion.lld:pubmed
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pubmed-article:18456387pubmed:articleTitleAlternative treatment paradigm for thalassemia using iron chelators.lld:pubmed
pubmed-article:18456387pubmed:affiliationDepartment of Physiology, Medicine, and Experimental Medicine, McGill University, Montreal, Quebec, Canada.lld:pubmed
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