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J M Saint-Remy

Showing results (71-80 of 79) with videos related to

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Thrombosis and Haemostasis|August 24, 1999
Some factor VIII (FVIII) inhibitors recognise a FVIII epitope(s) that is present only on FVIII-vWF complexesJ G Gilles, R Lavend'homme, K Peerlinck, et al.
Journal of Thrombosis and Haemostasis : JTH|February 12, 2009
A human monoclonal antibody inhibiting partially factor VIII activity reduces thrombus growth in baboonsM Jacquemin, J M Stassen, J-M Saint-Remy, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 19, 2014
Switching clotting factor concentrates: considerations in estimating the risk of immunogenicityD Matino, D Lillicrap, J Astermark, et al.
Blood|March 26, 1999
Antifactor VIII antibody inhibiting allogeneic but not autologous factor VIII in patients with mild hemophilia AK Peerlinck, M G Jacquemin, J Arnout, et al.
Blood|December 23, 1999
A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factorM Jacquemin, A Benhida, K Peerlinck, et al.
Blood|July 10, 1998
Mechanism and kinetics of factor VIII inactivation: study with an IgG4 monoclonal antibody derived from a hemophilia A patient with inhibitorM G Jacquemin, B G Desqueper, A Benhida, et al.
Journal of Thrombosis and Haemostasis : JTH|April 9, 2010
A human FVIII inhibitor modulates FVIII surface electrostatics at a VWF-binding site distant from its epitopeJ D Dimitrov, L T Roumenina, J-L Plantier, et al.
Journal of Thrombosis and Haemostasis : JTH|May 13, 2006
Variable region heavy chain glycosylation determines the anticoagulant activity of a factor VIII antibodyM Jacquemin, C M Radcliffe, R Lavend'homme, et al.
Blood|July 27, 2000
A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factorM Jacquemin, R Lavend'homme, A Benhida, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Thrombosis and Haemostasis|August 24, 1999
Some factor VIII (FVIII) inhibitors recognise a FVIII epitope(s) that is present only on FVIII-vWF complexesJ G Gilles, R Lavend'homme, K Peerlinck, et al.
Journal of Thrombosis and Haemostasis : JTH|February 12, 2009
A human monoclonal antibody inhibiting partially factor VIII activity reduces thrombus growth in baboonsM Jacquemin, J M Stassen, J-M Saint-Remy, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 19, 2014
Switching clotting factor concentrates: considerations in estimating the risk of immunogenicityD Matino, D Lillicrap, J Astermark, et al.
Blood|March 26, 1999
Antifactor VIII antibody inhibiting allogeneic but not autologous factor VIII in patients with mild hemophilia AK Peerlinck, M G Jacquemin, J Arnout, et al.
Blood|December 23, 1999
A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factorM Jacquemin, A Benhida, K Peerlinck, et al.
Blood|July 10, 1998
Mechanism and kinetics of factor VIII inactivation: study with an IgG4 monoclonal antibody derived from a hemophilia A patient with inhibitorM G Jacquemin, B G Desqueper, A Benhida, et al.
Journal of Thrombosis and Haemostasis : JTH|April 9, 2010
A human FVIII inhibitor modulates FVIII surface electrostatics at a VWF-binding site distant from its epitopeJ D Dimitrov, L T Roumenina, J-L Plantier, et al.
Journal of Thrombosis and Haemostasis : JTH|May 13, 2006
Variable region heavy chain glycosylation determines the anticoagulant activity of a factor VIII antibodyM Jacquemin, C M Radcliffe, R Lavend'homme, et al.
Blood|July 27, 2000
A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factorM Jacquemin, R Lavend'homme, A Benhida, et al.
Pageof 8