Author:
Musallam Khaled M.,Nasreddine Wassim,Beydoun Ahmad,Hourani Roula,Hankir Ahmed,Koussa Suzanne,Haidar Mohamad,Taher Ali T.
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Reference43 articles.
1. Taher AT, Musallam KM, Cappellini MD, Weatherall DJ (2011) Optimal management of β thalassaemia intermedia. Br J Haematol 152:512–523
2. Steinberg MH, Forget BG, Higgs DR, Weatherall DJ (2009) Disorders of hemoglobin: genetics pathophysiology, and clinical management, 2nd edn. Cambridge University Press, Cambridge
3. Cappellini MD, Motta I, Musallam KM, Taher AT (2010) Redefining thalassemia as a hypercoagulable state. Ann N Y Acad Sci 1202:231–236
4. Taher AT, Musallam KM, El-Beshlawy A, Karimi M, Daar S, Belhoul K, Saned MS, Graziadei G, Cappellini MD (2010) Age-related complications in treatment-naive patients with thalassaemia intermedia. Br J Haematol 150:486–489
5. Taher AT, Musallam KM, Karimi M, El-Beshlawy A, Belhoul K, Daar S, Saned MS, El-Chafic AH, Fasulo MR, Cappellini MD (2010) Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study. Blood 115:1886–1892
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