Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
Abstract Beta thalassemia is an inherited hemoglobin disorder resulting in chronic hemolytic anemia. The most common treatment for thalassemia is blood transfusion which is necessary to provide the patients with healthy red blood cells containing normal hemoglobin. Repeated blood transfusion leads...
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| Natura: | Artigo |
| Lingua: | Inglês |
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PAGEPress Publications
2014-08-01
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| Serie: | Mediterranean Journal of Hematology and Infectious Diseases |
| Soggetti: | |
| Accesso online: | https://mjhid.org/index.php/mjhid/article/view/1691 |
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