Ensuring the safety of blood donations from donors with thalassemia traits: addressing critical issues in Thailand
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Paiboonsukwong K, Jopang Y, Winichagoon P, Fucharoen S. Thalassemia in Thailand. Hemoglobin. 2022;46:53-7.
Fucharoen S, Winichagoon P. New updating into hemoglobinopathies. Int J Lab Hematol. 2012;34:559-65.
Fucharoen S, Winichagoon P. Thalassemia and abnormal hemoglobin. Int J Hematol. 2002;76 (Suppl 2):83-9.
Traivaree C, Boonyawat B, Monsereenusorn C, Rujkijyanont P, Photia A. Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children. Appl Clin Genet. 2018;11:23-30.
Tongsong T, Wanapirak C, Sirivatanapa P, Sa-nguansermsri T, Sirichotiyakul S, Piyamongkol W, et al. Prenatal eradication of Hb Bart's hydrops fetalis. J Reprod Med. 2001;46:18-22.
Viprakasit V, Ekwattanakit S. Clinical classification, screening and diagnosis for thalassemia. Hematol Oncol Clin North Am. 2018;32:193-211.
Fucharoen S, Weatherall DJ. The hemoglobin E thalassemias. Cold Spring Harb Perspect Med. 2012;2:a011734. doi. 10.1101/cshperspect.a011734.
Phengsavanh A, Sengchanh S, Souksakhone C, Souvanlasy B, Sychareun V. Current status of thalassemia in Lao People's Democratic Republic. Hemoglobin. 2022;46:58-61.
Fucharoen S, Winichagoon P. Haemoglobinopathies in southeast Asia. Indian J Med Res. 2011;134:498-506.
Tepakhan W, Kanjanaopas S, Sreworadechpisal K, Penglong T, Sripornsawan P, Wangchauy C, et al. Molecular epidemiology and hematological profiles of hemoglobin variants in southern Thailand. Sci Rep. 2024;14:9255.
Yamsri S, Sanchaisuriya K, Fucharoen G, Sae-Ung N, Ratanasiri T, Fucharoen S. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center. Prenat Diagn. 2010;30:540-6.
Weatherall DJ, Clegg JB. Inherited haemoglobin disorders: an increasing global health problem. Bull World Health Organ. 2001;79:704-12.
Winichagoon P, Kumbunlue R, Sirankapracha P, Boonmongkol P, Fucharoen S. Discrimination of various thalassemia syndromes and iron deficiency and utilization of reticulocyte measurements in monitoring response to iron therapy. Blood Cells Mol Dis. 2015;54:336-41.
Weatherall DJ. The global problem of genetic disease. Ann Hum Biol. 2005;32:117-22.
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