Do Transfusion Dependent E-Βeta Thalassemics Behave Differently from Patients with Βeta-Thalassemia Major?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-021-01401-4.pdf
Reference16 articles.
1. Weatherall DJ, Clegg JB. The Thalassaemia Syndromes. 4th Edition Wiley; 2008. https://doi.org/10.1002/9780470696705
2. Olivieri NF, Pakbaz Z, Vichinsky E. Hb E/beta-thalassaemia: a common & clinically diverse disorder. Indian J Med Res. 2011;134(4):522–31.
3. Datta P, Basu S, Chakravarty SB, Chakravarty A, Banerjee D, Chandra S, Chakrabarti A. Enhanced oxidative cross-linking of hemoglobin E with spectrin and loss of erythrocyte membrane asymmetry in hemoglobin Ebeta-thalassemia. Blood Cells Mol Dis. 2006;37(2):77–81. https://doi.org/10.1016/j.bcmd.2006.06.001.
4. Pootrakul P, Sirankapracha P, Hemsorach S, Moungsub W, Kumbunlue R, Piangitjagum A, Wasi P, Ma L, Schrier SL. A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in thai patients with thalassemia. Blood. 2000;96(7):2606–12.
5. Olivieri NF, Muraca GM, O'Donnell A, Premawardhena A, Fisher C, Weatherall DJ. Studies in haemoglobin E beta-thalassaemia. Br J Haematol. 2008 May;141(3):388–97. https://doi.org/10.1111/j.1365-2141.2008.07126.x.
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