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Effects of α-tocopherol on hemolysis and oxidative stress markers on red blood cells in β-thalassemia major
Background The accumulation of unpaired α-globin chains in patients with β-thalassemia major may clinically create ineffective erythropoiesis, hemolysis, and chronic anemia. Multiple blood transfusions and iron overload cause cellular oxidative damage. However, α-tocopherol, an antioxidant, is a pot...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Pediatric Society
2020-08-01
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| Colecção: | Clinical and Experimental Pediatrics |
| Assuntos: | |
| Acesso em linha: | http://www.e-cep.org/upload/pdf/cep-2019-00542.pdf |
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