Total Antioxidant Status in Patients with Major β-Thalassemia

OBJECTIVE: Beta-thalassemia major is an autosomal recessive disease causing severe and hemolytic anemia, which begins about 2-6 months after birth. Iron overload, which arises from recurrent transfusion and ineffective erythropoiesis, can enhance oxidative stress in thalassemic patients. The aim of...

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Detalles Bibliográficos
Autores principales: Bazvand, Fatemeh, Shams, Sedigheh, Borji Esfahani, Mahtab, Koochakzadeh, Lili, Monajemzadeh, Maryam, Ashtiani, Mohammad-Taghi Haghi, Rezaei, Nima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446157/
https://www.ncbi.nlm.nih.gov/pubmed/23056782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446157/
https://www.ncbi.nlm.nih.gov/pubmed/23056782

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