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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 5
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Original Article

Efficacy of Deferasirox (Exjade®) in Modulation of Iron Overload in Patients with β-Thalassemia Intermedia

Mehran KarimiHematology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran Correspondence[email protected]
,
Nargess ArandiHematology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran
,
Sezaneh HaghpanahHematology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran
,
Shahla AnsariIran University of Medical Sciences, Tehran, Iran
,
Azita AzarkeyvanIranian Blood Transfusion Organization, Tehran, Iran
,
Mohammadreza BordbarHematology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran
&
Sanaz SafaeiHematology Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran
show all
Pages 327-329 | Received 20 Oct 2014, Accepted 08 Feb 2015, Published online: 26 Jun 2015

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Read on this site (3)

Christina N Kontoghiorghe & George J Kontoghiorghes. (2016) Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. Drug Design, Development and Therapy 10, pages 465-481.
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Ali T Taher, John B Porter, Antonis Kattamis, Vip Viprakasit & M Domenica Cappellini. (2016) Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes. Drug Design, Development and Therapy 10, pages 4073-4078.
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Racha Halawi, Irene Motta, Ali Taher & Maria Domenica Cappellini. (2016) Deferasirox: an orphan drug for chronic iron overload in non-transfusion dependent thalassemia syndromes. Expert Opinion on Orphan Drugs 4:6, pages 677-686.
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Articles from other publishers (5)

U. U. Rakhmanova. (2022) Comparative characteristics of humoral immunity indicators and their relationship with chelation therapy in thalassemia. Meditsinskiy sovet = Medical Council:19, pages 162-166.
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Yen-Chien Lee, Chi-Tai Yen, Yen-Ling Lee & Rong-Jane Chen. (2022) Thalassemia Intermedia: Chelator or Not?. International Journal of Molecular Sciences 23:17, pages 10189.
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Daniel E. Radford-Smith, Elizabeth E. Powell & Lawrie W. Powell. (2018) Haemochromatosis: a clinical update for the practising physician. Internal Medicine Journal 48:5, pages 509-516.
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Flor Yus Cebrian, María del Valle Recasens Flores, Silvia Izquierdo Álvarez, Ingrid Parra Salinas & Carmen Rodriguez-Vigil Iturrate. (2016) Combination of a triple alpha-globin gene with beta-thalassemia in a gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children. BMC Research Notes 9:1.
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Sim Y. Ong, Amanda J. Nicoll & Martin B. Delatycki. (2016) How should hyperferritinaemia be investigated and managed?. European Journal of Internal Medicine 33, pages 21-27.
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