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Methods in Molecular Medicine|February 23, 2011
Detection of DNA by silver stainingD J Perry, F PeyvandiThrombosis and Haemostasis|November 1, 2000
Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VIIF Peyvandi, P M Mannucci, P V Jenkins, et al.Thrombosis and Haemostasis|August 26, 2000
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiencyF Peyvandi, P V Jenkins, P M Mannucci, et al.British Journal of Haematology|February 26, 2000
A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarctionF Peyvandi, P M Mannucci, P Bucciarelli, et al.Blood|February 13, 2001
Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15-base pair insertion in the F7 geneF Peyvandi, J A Carew, D J Perry, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 15, 2009
Combined FV and FVIII deficiencyM Spreafico, F PeyvandiHaemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2016
Genomic approaches to bleeding disordersF Peyvandi, C P M HaywardAnnali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|February 24, 2001
Apparently dominant transmission of a recessive disease: deficiency of factor VII in Iranian JewsL Tagliabue, F Duca, F PeyvandiJournal of Thrombosis and Haemostasis : JTH|July 26, 2011
Gynecological and obstetrical manifestations of inherited bleeding disorders in womenF Peyvandi, I Garagiola, M MenegattiPageof 24