Normalized levels of red blood cells expressing phosphatidylserine, their microparticles, and activated platelets in young patients with β-thalassemia following bone marrow transplantation
Author:
Funder
Thailand Research Fund
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/article/10.1007/s00277-017-3070-2/fulltext.html
Reference31 articles.
1. Fucharoen S, Winichagoon P (2002) Thalassemia and abnormal hemoglobin. Int J Hematol 76(Suppl 2):83–89
2. Fucharoen S, Winichagoon P (2011) Haemoglobinopathies in southeast Asia. Indian J Med Res 134:498–506
3. Hongeng S, Pakakasama S, Chaisiripoomkere W, Chuansumrit A, Sirachainan N, Ungkanont A et al (2004) Outcome of transplantation with unrelated donor bone marrow in children with severe thalassaemia. Bone Marrow Transplant 33(4):377–379
4. Anurathapan U, Hongeng S, Pakakasama S, Sirachainan N, Songdej D, Chuansumrit A et al (2016) Hematopoietic stem cell transplantation for homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients from haploidentical donors. Bone Marrow Transplant 51(6):813–818
5. Issaragrisil S, Kunacheewa C (2016) Matched sibling donor hematopoietic stem cell transplantation for thalassemia. Curr Opin Hematol 23(6):508–514
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