Non-transferrin bound labile plasma iron and iron overload in Sickle Cell Disease: a comparative study between Sickle Cell Disease and Î² thalassemic patients-Reference-Cited by-同舟云学术

Non-transferrin bound labile plasma iron and iron overload in Sickle Cell Disease: a comparative study between Sickle Cell Disease and Î² thalassemic patients

Published:2010-01 Issue:1 Volume:84 Page:72-78
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Koren Ariel,Fink Daniel,Admoni Osnat,Tennenbaum-Rakover Yardena,Levin Carina

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2009.01342.x/fullpdf

Reference23 articles.

1. Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: a report from the multi-center study of iron overload;Fung;Am J Hematol,2007

2. Iron overload is a determinant of morbidity and mortality in adult patients with sickle cell disease;Ballas;Semin Hematol,2001

3. Comparison of organ dysfunction in transfused patients with SCD or beta thalassemia;Vichinsky;Am J Hematol,2005

4. Myocardial iron loading in transfusion-dependent thalassemia and sickle cell disease;Wood;Blood,2004

5. Magnetic resonance imaging in the evaluation of iron overload in patients with beta thalassaemia and sickle cell disease;Voskaridou;Br J Haematol,2004

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