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Haemophilia : the Official Journal of the World Federation of Hemophilia|June 23, 2011
Prenatal diagnosis and preimplantation genetic diagnosis: novel technologies and state of the art of PGD in different regions of the worldF Peyvandi, I Garagiola, M MortarinoJournal of Thrombosis and Haemostasis : JTH|September 4, 2016
Advances in the treatment of bleeding disordersF Peyvandi, I Garagiola, E BiguzziJournal of Thrombosis and Haemostasis : JTH|July 2, 2013
Future of coagulation factor replacement therapyF Peyvandi, I Garagiola, S SeregniHaemophilia : the Official Journal of the World Federation of Hemophilia|February 22, 2017
Molecular diagnosis of von Willebrand diseaseL Baronciani, A Goodeve, F PeyvandiReviews in Clinical and Experimental Hematology|February 15, 2002
Autosomal recessive deficiencies of coagulation factorsF Peyvandi, R Asselta, P M MannucciBritish Journal of Haematology|February 13, 2001
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand diseaseM Lak, F Peyvandi, P M MannucciJournal of Thrombosis and Haemostasis : JTH|December 15, 2015
A critical appraisal of one-stage and chromogenic assays of factor VIII activityF Peyvandi, J Oldenburg, K D FriedmanMethods in Molecular Medicine|February 23, 2011
Screening for Mutations in the Human Antithrombin Gene by Hydrolink D-5000™ and MDE™ Gel ElectrophoresisD J PerryBlood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 1, 1995
Ectopic transcript analysis in human antithrombin deficiencyD J PerryPageof 24