Role of deferiprone in chelation therapy for transfusional iron overload

Author:

Hoffbrand A. Victor1,Cohen Alan1,Hershko Chaim1

Affiliation:

1. From the Department of Haematology, Royal Free Hospital, London, United Kingdom; the Division of Hematology, Children's Hospital of Philadelphia, PA; and the Department of Medicine, Share Zedek Medical Centre, Jerusalem, Israel.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference91 articles.

1. Zurlo MG, De Stefano P, Borgna-Pignatti C, et al. Survival and causes of death in thalassaemia major. Lancet.1989;2: 27-30.

2. Borgna-Pignatti C, Carnelli V, Caruso V, et al. Survival and disease complications in thalassemia major. Ann N Y Acad Sci.1998;850: 227-231.

3. World Health Organisation Hereditary Diseases Programme. Guidelines for the Control of Haemoglobin Disorders Booklet.1994; WHO/HDP/HB/GL/94.1.

4. Pippard MJ, Weatherall DJ. Oral iron chelation therapy for thalassaemia: an uncertain scene. Br J Haematol.2000;111: 2-5.

5. Balveer K, Pryor K, Wonke B. Combined oral and parenteral iron chelation in beta thalassaemia major. Med J Malaysia.2001;55: 493-497.

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