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Blood|February 1, 1993
Increased thrombin generation in a child with a combined factor IX and protein C deficiencyC Negrier, M Berruyer, A Durin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 21, 2011
On-demand treatment of bleeds in haemophilia patients with inhibitors: strategies for securing and maintaining predictable efficacy with recombinant activated factor VIIB Sørensen, Y Dargaud, G Kenet, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 12, 2016
Dosing regimens, FVIII levels and estimated haemostatic protection with special focus on rFVIIIFcE Berntorp, C Negrier, P Gozzi, et al.
Journal of Thrombosis and Haemostasis : JTH|October 31, 2009
Activated factor X cleaves factor VIII at arginine 562, limiting its cofactor efficiencyJ L Plantier, V Rolli, C Ducasse, et al.
Journal of Thrombosis and Haemostasis : JTH|May 25, 2011
Thrombin generation assay using factor IXa as a trigger to quantify accurately factor VIII levels in haemophilia AM Ninivaggi, Y Dargaud, R van Oerle, et al.
Thrombosis and Haemostasis|June 1, 1997
Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. French FEIBA Study Group. Factor Eight Bypassing ActivityC Negrier, J Goudemand, Y Sultan, et al.
American Journal of Hematology|July 1, 1994
Increased thrombosis incidence in a family with an inherited protein S deficiency and a high oxygen affinity hemoglobin variantM Berruyer, A Francina, P Ffrench, et al.
Thrombosis Journal|April 12, 2018
Combined life-threatening thromboses and hemorrhages in a patient with afibrinogenemia and antithrombin deficiencyS Le Quellec, A Desjonqueres, L Rugeri, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 27, 2012
The potential role of synovial thrombomodulin in the pathophysiology of joint bleeds in haemophiliaY Dargaud, H Simpson, Y Chevalier, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 9, 2012
Use of Haemate(®) P as immune tolerance induction in patients with severe haemophilia A who failed previous induction attempts: a multicentre observational studyC Rothschild, R D'Oiron, A Borel-Derlon, et al.
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