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Nutritional deficiencies in iron overloaded patients with hemoglobinopathies
One of the hallmarks of both sickle cell disease (SCD) and thalassemia major (TM) is accelerated oxidative damage. Decreased antioxidant levels and increased oxidant stress biomarkers are found in both diseases. Although isolated vitamin deficiencies have been reported in TM and nontransfused SCD pa...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2887656/ https://ncbi.nlm.nih.gov/pubmed/19415722 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.21416 |
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