Effects of three months of treatment with vitamin E and N-acetyl cysteine on the oxidative balance in patients with transfusion-dependent β-thalassemia
Author:
Funder
Vice-Chancellor for Research, Shiraz University of Medical Sciences
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-020-04346-2.pdf
Reference36 articles.
1. Ozdemir ZC, Koc A, Aycicek A, Kocyigit A (2014) N-acetylcysteine supplementation reduces oxidative stress and DNA damage in children with β-thalassemia. Hemoglobin 38(5):359–364
2. Kassab-Chekir A, Laradi S, Ferchichi S, Khelil AH, Feki M, Amri F, Selmi H, Bejaoui M, Miled A (2003) Oxidant, antioxidant status and metabolic data in patients with beta-thalassemia. Clin Chim Acta 338(1-2):79–86
3. Rachmilewitz EA, WEIZER-STERN O, Adamsky K, Amariglio N, Rechavi G, Breda L, Rivella S, Cabantchik ZI (2005) Role of iron in inducing oxidative stress in thalassemia: can it be prevented by inhibition of absorption and by antioxidants? Ann N Y Acad Sci 1054(1):118–123
4. Fibach E, Rachmilewitz EA (2017) Pathophysiology and treatment of patients with beta-thalassemia–an update. F1000Res 6:2156
5. Tesoriere L, D’Arpa D, Butera D, Allegra M, Renda D, Maggio A, Bongiorno A, Livrea MA (2001) Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in β-thalassemia intermedia patients. Free Radic Res 34(5):529–540
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1. Can N-acetylcysteine reduce red blood cell transfusion burden in patients with transfusion-dependent β-thalassemia?;Pediatric Hematology and Oncology;2023-12-13
2. The effect of Vitamin E and N-acetyl cysteine on oxidative status and hemoglobin level in transfusion-dependent thalassemia patients: A systematic review and meta-analysis;Iranian Journal of Blood and Cancer;2023-03-01
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