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Bibliotheca Haematologica|January 1, 1985
G6PD encapsulation and metabolic properties of loaded erythrocytesG Fiorelli, T Ploner, W Berardi, et al.Transplantation|February 1, 1975
A modified rosette inhibition test in renal allotransplantationA Cantaluppi, C Ponticelli, F Salerno, et al.Clinical Genetics|January 6, 2007
Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyriaE Di Pierro, V Brancaleoni, V Moriondo, et al.Journal of Thrombosis and Haemostasis : JTH|March 9, 2011
Thalassemia trait and arterial thromboembolic events: a systematic review and a meta-analysis of the literatureF Dentali, E Romualdi, W Ageno, et al.Canadian Journal of Gastroenterology = Journal Canadien De Gastroenterologie|December 8, 2000
Iron and liver diseasesS Fargion, M Mattioli, A L Fracanzani, et al.Cardiovascular & Hematological Disorders Drug Targets|September 28, 2007
Heparin induced thrombocytopenia: pathogenetic, clinical, diagnostic and therapeutic aspectsR Castelli, E Cassinerio, M D Cappellini, et al.Acta Haematologica|July 1, 2006
Lung function in beta-thalassemia patients: a longitudinal studyG Piatti, L Allegra, V Fasano, et al.Diabetic Medicine : a Journal of the British Diabetic Association|March 31, 2004
Unreliable estimation of HbA due to the presence of Camperdown haemoglobin [beta 104 (G6) Arg --> Ser]R Castelli, A Tempesta, A Bianchi, et al.International Journal of Laboratory Hematology|March 9, 2011
Nontransferrin-bound iron in transfused patients with sickle cell diseaseA Inati, K M Musallam, M D Cappellini, et al.Blood Cells, Molecules & Diseases|February 6, 2008
Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patientsC L Harteveld, C Refaldi, E Cassinerio, et al.Pageof 23