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F Peyvandi

Showing results (121-130 of 166) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|May 21, 2016
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agentsM E Mancuso, V Chantarangkul, M Clerici, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 12, 2014
Management of orthopaedic surgery in rare bleeding disordersS M Siboni, E Biguzzi, G Pasta, et al.
British Journal of Haematology|July 19, 2006
Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantationF Peyvandi, S M Siboni, D Lambertenghi Deliliers, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 1, 1997
Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenariansP M Mannucci, D Mari, G Merati, et al.
Journal of Thrombosis and Haemostasis : JTH|June 4, 2015
Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-moduleR Asselta, M Robusto, P Braidotti, 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|December 17, 2013
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutationsM Borhany, H Handrkova, A Cairo, et al.
Journal of Thrombosis and Haemostasis : JTH|May 12, 2010
Active platelet-binding conformation of plasma von Willebrand factor in young women with acute myocardial infarctionF Peyvandi, M J Hollestelle, R Palla, et al.
Blood|December 12, 2001
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAsR Asselta, S Duga, S Spena, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature diseaseP M Mannucci, R Asselta, S Duga, et al.
Pageof 17

Showing results (121-130 of 166) with videos related to

Sort By:
Pageof 17
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 21, 2016
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agentsM E Mancuso, V Chantarangkul, M Clerici, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 12, 2014
Management of orthopaedic surgery in rare bleeding disordersS M Siboni, E Biguzzi, G Pasta, et al.
British Journal of Haematology|July 19, 2006
Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantationF Peyvandi, S M Siboni, D Lambertenghi Deliliers, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 1, 1997
Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenariansP M Mannucci, D Mari, G Merati, et al.
Journal of Thrombosis and Haemostasis : JTH|June 4, 2015
Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-moduleR Asselta, M Robusto, P Braidotti, 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|December 17, 2013
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutationsM Borhany, H Handrkova, A Cairo, et al.
Journal of Thrombosis and Haemostasis : JTH|May 12, 2010
Active platelet-binding conformation of plasma von Willebrand factor in young women with acute myocardial infarctionF Peyvandi, M J Hollestelle, R Palla, et al.
Blood|December 12, 2001
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAsR Asselta, S Duga, S Spena, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature diseaseP M Mannucci, R Asselta, S Duga, et al.
Pageof 17