Iron chelation therapy in the management of thalassemia: the Asian perspectives

Author:

Viprakasit Vip,Lee-Lee Chan,Chong Quah Thuan,Lin Kai-Hsin,Khuhapinant Archrob

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Reference72 articles.

1. Weatherall DJ, Clegg JB. Inherited haemoglobin disorders: an increasing global health problem. Bull World Health Organ. 2001;79:704–12.

2. Weatherall DJ, Clegg JB, editors. The Thalassaemia Syndromes. 4th ed. Oxford: Blackwell Science; 2001.

3. Higgs D. Molecular mechanisms of α thalassemia. In: Steinberg M, Forget B, Higgs D, Nagel R, editors. Disorders of hemoglobin. Cambridge: Cambridge University Press; 2001. p. 405–30.

4. Forget BG. Molecular mechanisms of β thalassemia. In: Steinberg MH, Forget BG, Higgs DR, Nagel RL, editors. Disorders of hemoglobin. Cambridge: Cambridge University Press; 2001. p. 252–76.

5. Viprakasit V, Kidd AM, Ayyub H, Horsley S, Hughes J, Higgs DR. De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia. Br J Haematol. 2003;120:867–75.

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