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Comment on: oxidative stress and antioxidant status in beta-thalassemia heterozygotes.
Rev Bras Hematol Hemoter. 2013;35(6):385-6. doi: 10.5581/1516-8484.20130125.
2
Oxidative stress and antioxidant status in beta-thalassemia heterozygotes.
Rev Bras Hematol Hemoter. 2013;35(6):409-13. doi: 10.5581/1516-8484.20130122.
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Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey.
Free Radic Biol Med. 2021 Apr;166:337-347. doi: 10.1016/j.freeradbiomed.2021.02.028. Epub 2021 Mar 4.
6
Bilirubin concentrations in thalassemia heterozygotes in university students.
Eur J Haematol. 2011 Apr;86(4):317-23. doi: 10.1111/j.1600-0609.2011.01578.x.
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Lipid peroxidation and antioxidant status in beta-thalassemia.
Pediatr Hematol Oncol. 2000 Dec;17(8):687-93. doi: 10.1080/08880010050211402.

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Pattern of β-Thalassemia and Other Haemoglobinopathies: A Cross-Sectional Study in Bangladesh.
ISRN Hematol. 2012;2012:659191. doi: 10.5402/2012/659191. Epub 2012 Jun 14.
2
Immunological evaluation of patients with beta-thalassemia major.
Acta Haematol. 2001;105(1):7-12. doi: 10.1159/000046526.
3
Lipid peroxidation and antioxidant status in beta-thalassemia.
Pediatr Hematol Oncol. 2000 Dec;17(8):687-93. doi: 10.1080/08880010050211402.
6
Catalase: a tetrameric enzyme with four tightly bound molecules of NADPH.
Proc Natl Acad Sci U S A. 1984 Jul;81(14):4343-7. doi: 10.1073/pnas.81.14.4343.
7
Catalase activity and red cell metabolism.
Adv Exp Med Biol. 1972;28:121-31. doi: 10.1007/978-1-4684-3222-0_8.
8
Antioxidant system and serum trace elements in alpha-thalassaemia and Hb Lepore trait.
Eur J Haematol. 1987 Jul;39(1):23-7. doi: 10.1111/j.1600-0609.1987.tb00158.x.

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