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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 3
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Original Article

Preventable Severe Thalassemia among Children

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Pages 148-153 | Received 13 Mar 2018, Accepted 22 Jun 2018, Published online: 12 Sep 2018

References

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  • Fucharoen S, Winichagoon P, Pootrakul P, et al. Variable severity of Southeast Asian β0-thalassemia/Hb E disease. Birth Defects Orig Artic Ser. 1987;23(5A):241–248.
  • Winichagoon P, Thonglairoam V, Fucharoen S, et al. Severity differences in β-thalassaemia/haemoglobin E syndromes: implication of genetic factors. Br J Haematol. 1993;83(4):633–639.
  • Viprakasit V, Raffaella O. Genetic basis, pathophysiology and diagnosis. In: Cappellini MD, Cohen A, Porter J, et al., Eds. Guidelines for the Management of Transfusion Dependent Thalassemia (TDT). Nicosia (Cyprus): Thalassaemia International Federation; 2014:14–27.
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  • Clinical Practice Guidelines for diagnosis and management of thalassemia syndromes, 2014. Queen Sirikit National Institute of Child Health, Bangkok, Thailand, developed by the Thalassemia Foundation of Thailand, Bangkok, Thailand.
  • Rujito L, Basalamah M, Siswandari W, et al. Modifying effect of XmnI, BCL 11A and HBS1L-MYB on clinical appearances: a study on β-thalassemia and Hemoglobin E/β-thalassemia patients in Indonesia. Hematol Oncol Stem Cell Ther. 2016;9(2):55–63.
  • Lai Y, Chen Y, Chen B, et al. Genetic variants at BCL11A and HBS1L-MYB loci influence Hb F levels in Chinese Zhuang β-thalassemia intermedia patients. Hemoglobin. 2016;40(6):405–410.
  • Fucharoen S, Weatherall DJ. Progress toward the control and management of the Thalassemias. Hematol Oncol Clin North Am. 2016;30(2):359–371.
  • Fucharoen G, Sanchaisuriya K, Sae-ung N, et al. A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia. Bull World Health Organ. 2004;82(5):364–372.
  • Sindhuphak R, Kaewsuk O, Havanond P, et al. Appropriate screening model for thalassemia carriers in developing countries. J Hematol Transfus Med. 1996;3(3):165–177.

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