References
- Origa R. β-Thalassemia. Genet Med. 2017;19(6):609–619.
- Taher AT, Musallam KM, Cappellini MD. β-Thalassemias. N Engl J Med. 2021;384(8):727–743.
- Lee J-S, Cho SI, Park SS, Seong M-W. Molecular basis and diagnosis of thalassemia. Blood Res. 2021;56(S1):S39–S43.
- Winichagoon P, Kumbunlue R, Sirankapracha P, et al. Discrimination of various thalassemia syndromes and iron deficiency and utilization of reticulocyte measurements in monitoring response to iron therapy. Blood Cells Mol Dis. 2015;54(4):336–341.
- Langhi D Jr, Ubiali EM, Marques JF Jr, et al. Guidelines on beta-thalassemia major - regular blood transfusion therapy: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular: project guidelines: Associação Médica Brasileira - 2016. Rev Bras Hematol Hemoter. 2016;38(4):341–345.
- Cappellini MD, Cohen A, Eleftheriou A, et al. Iron overload. In: Cappellini MD, Cohen A, Porter J, et al. Editors. Guidelines for the Clinical Management of Thalassaemia, 2nd Revised ed. [Internet]. Nicosia (Cyprus): Thalassaemia International Federation, 2008.
- Porter J, Viprakasit V, et al. Iron overload and chelation. In: Cappellini MD, Cohen A, Porter J, Editors. Guidelines for the Management of Transfusion Dependent Thalassaemia (TDT), 3rd ed. [Internet]. Nicosia (CY): Thalassaemia International Federation; 2014.
- Susanah S, Idjradinata PS, Sari NM, et al. Time to start delivering iron chelation therapy in newly diagnosed severe β-thalassemia. Biomed Res Int. 2020;2020:1–6.
- Cappellini MD, Bejaoui M, Agaoglu L, et al. Iron chelation with deferasirox in adult and pediatric patients with thalassemia major: efficacy and safety during 5 years’ follow-up. Blood. 2011;118(4):884–893.
- Porter JB, El-Alfy M, Viprakasit V, et al. Utility of labile plasma iron and transferrin saturation in addition to serum ferritin as iron overload markers in different underlying anemias before and after deferasirox treatment. Eur J Haematol. 2016;96(1):19–26.
- Nisbet-Brown E, Olivieri NF, Giardina PJ, et al. Effectiveness and safety of ICL670 in iron-loaded patients with thalassaemia: a randomised, double-blind, placebo-controlled, dose-escalation trial. Lancet. 2003;361(9369):1597–1602.
- Ahmed J, Ahmad N, Jankharia B, et al. Effect of deferasirox chelation on liver iron and total body iron concentration. Indian J Pediatr. 2013;80(8):655–658.
- Xia S, Zhang W, Huang L, et al. Comparative efficacy and safety of deferoxamine, deferiprone and deferasirox on severe thalassemia: a meta-analysis of 16 randomized controlled trials. PLoS One. 2013;8(12):e82662.
- Sheth S. Iron chelation: an update. Curr Opin Hematol. 2014;21(3):179–185.
- Di Maggio R, Maggio A. The new era of chelation treatments: effectiveness and safety of 10 different regimens for controlling iron overloading in thalassaemia major. Br J Haematol. 2017;178(5):676–688.
- Jahir SJ, Anwar S, Morshed AKMA, et al. Effect of deferiprone versus deferiprone with deferasirox in iron chelation therapy of thalassemia children. J Med Sci Clin Res. 2018;6(9):330–336.
- Colah R, Italia K, Gorakshakar A. Burden of thalassemia in India: the road map for control. Pediatr Hematol Oncol J. 2017;2(4):79–84.
- Petrou M. Screening for beta thalassaemia. Indian J Hum Genet. 2010;16(1):1–5.
- Thiyagarajan A. Advancement in thalassemia treatment: a view from gene therapy. Clin Pharmacol Biopharm. 2018;07 (01):e131.
- Verma IC, Saxena R, Kohli S. Present & future scenario of thalassaemic care & control in India. Indian J Med Res. 2011;134(4):507–521.
- Mourad FH, Hoffbrand AV, Sheikh-Taha M, et al. Comparison between desferrioxamine and combined therapy with desferrioxamine and deferiprone in iron overloaded thalassaemia patients. Br J Haematol. 2003;121(1):187–189.
- Lai Y-R, Liu R-R, Li C-F, et al. Efficacy of deferasirox for the treatment of iron overloads in Chinese thalassemia major patients: results from a prospective, open-label, multicentre clinical trial. Transfusion Med. 2013;23(6):389–396.
- Jaiswal S, Hishikar R, Khandwal O, et al. Efficacy of deferasirox as an oral iron chelator in paediatric thalassaemia patients. J Clin Diagn Res. 2017;11(2):FC01–FC03.
- Cappellini MD, Musallam KM, Taher AT. Overview of iron chelation therapy with desferrioxamine and deferiprone. Hemoglobin. 2009;33(sup1):S58–S569.
- Cohen AR, Galanello R, Piga A, et al. Safety and effectiveness of long-term therapy with the oral iron chelator deferiprone. Blood. 2003;102(5):1583–1587.
- Taher A, El-Beshlawy A, Elalfy MS, et al. Efficacy and safety of deferasirox, an oral iron chelator, in heavily iron-overloaded patients with β-thalassaemia: the ESCALATOR study. Eur J Haematol. 2009;82(6):458–465.
- Peng C-T, Chow K-C, Chen J-H, et al. Safety monitoring of cardiac and hepatic systems in beta-thalassemia patients with chelating treatment in Taiwan . Eur J Haematol. 2003;70(6):392–397.
- Pennell DJ, Porter JB, Cappellini MD, et al. Efficacy of deferasirox in reducing and preventing cardiac iron overload in beta-thalassemia. Blood. 2010;115(12):2364–2371.
- Roberts DJ, Brunskill SJ, Doree C, et al. Oral deferiprone for iron chelation in people with thalassaemia. Cochrane Database Syst Rev. 2007;3:CD004839.