Genotype–phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12185-011-0985-6.pdf
Reference29 articles.
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2. Kattamis A. Treatment of thalassemia with hydroxyurea: an indispensable alternative therapy. J Pediatr Hematol Oncol. 2007;29:729–30.
3. Bradai M, Abad MT, Pissard S, Lamraoui F, Skopinski L, de Montalembert M. Hydroxyurea can eliminate transfusion requirements in children with severe beta-thalassemia. Blood. 2003;102:1529–30.
4. Hoppe C, Vichinsky E, Lewis B, Foote D, Styles L. Hydroxyurea and sodium phenylbutyrate therapy in thalassemia intermedia. Am J Hematol. 1999;62:221–7.
5. Karimi M. Hydroxyurea in the management of thalassemia intermedia. Hemoglobin. 2009;33(Suppl 1):S177–82.
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