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Archives of Disease in Childhood|January 1, 1994
Effect of alpha thalassaemia trait and enhanced gamma chain production on disease severity in beta thalassaemia major and intermediaP Gringras, B Wonke, J Old, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2001
Management of puberty for optimal auxological results in beta-thalassaemia majorM Caruso-Nicoletti, V De Sanctis, L Cavallo, et al.Journal of Clinical Pathology|July 1, 1994
Zinc concentration in patients with iron overload receiving oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one or desferrioxamineF N al-Refaie, B Wonke, D G Wickens, et al.British Medical Journal (Clinical Research Ed.)|December 12, 1987
Effective chelation of iron in beta thalassaemia with the oral chelator 1,2-dimethyl-3-hydroxypyrid-4-oneG J Kontoghiorghes, M A Aldouri, A V Hoffbrand, et al.Lancet (London, England)|June 25, 1983
Use of bone-marrow culture in prediction of acute leukaemic transformation in preleukaemiaG E Francis, M A Wing, E J Miller, et al.Blood|August 1, 1992
Efficacy and possible adverse effects of the oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one (L1) in thalassemia majorF N al-Refaie, B Wonke, A V Hoffbrand, et al.British Journal of Haematology|November 5, 1997
Combination therapy with interferon alpha and ribavirin for chronic hepatitis C virus infection in thalassaemic patientsP T Telfer, J A Garson, K Whitby, et al.British Journal of Haematology|September 1, 1995
Results of long-term deferiprone (L1) therapy: a report by the International Study Group on Oral Iron ChelatorsF N al-Refaie, C Hershko, A V Hoffbrand, et al.Blood|February 1, 1996
Moderate reduction of beta-globin gene transcript by a novel mutation in the 5' untranslated region: a study of its interaction with other genotypes in two familiesP J Ho, J Rochette, C A Fisher, et al.Blood|October 1, 1996
Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiencyD C Rees, J Duley, H A Simmonds, et al.Pageof 7