Australian guidelines for the assessment of iron overload and iron chelation in transfusion-dependent thalassaemia major, sickle cell disease and other congenital anaemias

Author:

Ho P. J.,Tay L.,Lindeman R.,Catley L.,Bowden D. K.

Publisher

Wiley

Subject

Internal Medicine

Reference48 articles.

1. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine;Borgna-Pignatti;Haematologica,2004

2. Survival in beta-thalassaemia major in the UK: data from the UK Thalassaemia Register;Modell;Lancet,2000

3. Which psychosocial factors are related to chelation adherence in thalassemia? A systematic review;Evangeli;Hemoglobin,2010

4. Iron-chelating therapy and the treatment of thalassemia;Olivieri;Blood,1997

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