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Lancet (London, England)|January 8, 2008
Glucose-6-phosphate dehydrogenase deficiencyM D Cappellini, G FiorelliBritish Journal of Haematology|August 1, 1981
Interaction between homozygous beta (0) thalassaemia and the Swiss type of hereditary persistence of fetal haemoglobinM D Cappellini, G Fiorelli, L F BerniniAmerican Journal of Hematology|October 1, 1991
Effect of estrogens and progesterone on human peripheral erythroid burst-forming unit (BFU-E) growthT M De Feo, M D Cappellini, G FiorelliBailliere'S Best Practice & Research. Clinical Haematology|August 5, 2000
Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variantsG Fiorelli, F Martinez di Montemuros, M D CappelliniAnnali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|November 4, 2000
A case of pulmonary thromboembolism in thalassemia intermedia: are these patients at risk for thrombotic events?L Ciceri, M Amato, M D Cappellini, et al.Scandinavian Journal of Haematology|February 1, 1981
Non-specific iron in patients with beta-thalassaemia trait and chronic active hepatitisS Fargion, M D Cappellini, M Sampietro, et al.Haematologica|September 1, 1990
Iron metabolism in thalassemia intermediaG Fiorelli, S Fargion, A Piperno, et al.Hemoglobin|December 22, 1998
Indices of membrane alterations in beta-thalassemic erythrocytesD Tavazzi, A Comino, F Turrini, et al.Annals of the New York Academy of Sciences|December 13, 2005
Coagulation and splenectomy: an overviewM D Cappellini, E Grespi, E Cassinerio, et al.Acta Haematologica|January 1, 1982
The iron status of Italian subjects with beta-thalassemia traitS Fargion, M T Taddei, M D Cappellini, et al.Pageof 23