Effect of α-Chain Precipitates on Bone Marrow Function in Homozygous β-Thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1973.tb01721.x/fullpdf
Reference13 articles.
1. Intracellular Loss of Free α Chains in β Thalassaemia
2. Inclusions of Hemoglobin in Erythroblasts and Erythrocytes of Thalassemia
3. Hemoglobin metabolism in thalassemia
4. Iron Deficiency and Dyserythropoiesis
5. Simultaneous Radioactive Tracer Studies of Erythropoiesis and Red-Cell Destruction in Thalassaemia
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1. Electron Microscope Autoradiographic Studies of the Erythroblasts of a Case of Congenital Dyserythropoietic Anaemia, Type II;Scandinavian Journal of Haematology;2009-04-24
2. Ferrokinetic and erythrokinetic studies in alpha and beta thalassaemia;Clinical & Laboratory Haematology;2008-06-28
3. The Morphology and Kinetics of Erythropoiesis in Homozygous β-Thalassaemia;Novartis Foundation Symposia;2008-05-30
4. Iron release in erythrocytes from patients withβ-thalassemia;Free Radical Research;1999-01
5. Composition of the intra-erythroblastic precipitates in thalassaemia and congenital dyserythropoietic anaemia (CDA): identification of a new type of CDA with intra-erythroblastic precipitates not reacting with monoclonal antibodies to alpha- and beta-globin chains;British Journal of Haematology;1996-06
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