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Anemia|August 28, 2012
Health-Related Quality of Life, Treatment Satisfaction, Adherence and Persistence in β-Thalassemia and Myelodysplastic Syndrome Patients with Iron Overload Receiving Deferasirox: Results from the EPIC Clinical TrialJohn Porter, Donald K Bowden, Marina Economou, et al.Hemasphere|November 15, 2019
Cardiac and hepatic siderosis in myelodysplastic syndrome, thalassemia and diverse causes of transfusion-dependent anemia: the TIMES studyP Joy Ho, Devendra Hiwase, Raj Ramakrishna, et al.European Journal of Haematology|August 19, 2016
Cardiac iron load and function in transfused patients treated with deferasirox (the MILE study)P Joy Ho, Lay Tay, Juliana Teo, et al.Internal Medicine Journal|September 12, 2017
Urolithiasis is prevalent and associated with reduced bone mineral density in β-thalassaemia majorPhillip Wong, Frances Milat, Peter J Fuller, et al.Pathology|March 31, 2007
Complex phenotypes in the haemoglobinopathies: recommendations on screening and DNA testingRonald J Trent, Boyd Webster, Donald K Bowden, et al.International Journal of Hematology|March 5, 2011
Clinical efficacy and safety evaluation of tailoring iron chelation practice in thalassaemia patients from Asia-Pacific: a subanalysis of the EPIC study of deferasiroxVip Viprakasit, Hishamshah Ibrahim, Shau-Yin Ha, et al.Pageof 2