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C Négrier

Showing results (1-10 of 45) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
A retrospective postlicensure survey of FEIBA efficacy and safetyD Dimichele, C Négrier
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 13, 2000
Overall experience with NovoSevenC Négrier, A Lienhart
Acta Haematologica|January 1, 1991
Successful treatment of acquired factor VIII antibody by extracorporeal immunoadsorptionC Négrier, M Dechavanne, F Alfonsi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
An unusual haemarthrosis in an HIV-seronegative haemophilia A patientC Ménart, P Duhaut, O Attali, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 18, 1998
Levels of prothrombin activation peptide F1+2 in patients with a bleeding tendencyJ Ingerslev, M Holm, K Christiansen, et al.
International Journal of Laboratory Hematology|October 6, 2017
Comparison of an automated chemiluminescent assay to a manual ELISA assay for determination of von Willebrand Factor collagen binding activity on VWD plasma patients previously diagnosed through molecular analysis of VWFE Jousselme, Y Jourdy, L Rugeri, et al.
Journal of Thrombosis and Haemostasis : JTH|November 13, 2018
Performance of a recombinant fusion protein linking coagulation factor IX with recombinant albumin in one-stage clotting assaysC Horn, C Négrier, U Kalina, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 1, 1999
Safety and efficacy of three arthroscopic procedures using Holmium: Yag laser in two high-responder haemophiliacsC Ménart, J J Lalain, A Lienhart, et al.
Thrombosis and Haemostasis|August 28, 2001
A factor VIII minigene comprising the truncated intron I of factor IX highly improves the in vitro production of factor VIIIJ L Plantier, M H Rodriguez, N Enjolras, et al.
Thrombosis and Haemostasis|August 1, 1996
Combined hereditary disorders of haemophilia B Leyden (-6 G-->A) and type 1 von Willebrand diseaseG Pernod, C Vinciguerra, C Gaucher, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
A retrospective postlicensure survey of FEIBA efficacy and safetyD Dimichele, C Négrier
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 13, 2000
Overall experience with NovoSevenC Négrier, A Lienhart
Acta Haematologica|January 1, 1991
Successful treatment of acquired factor VIII antibody by extracorporeal immunoadsorptionC Négrier, M Dechavanne, F Alfonsi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
An unusual haemarthrosis in an HIV-seronegative haemophilia A patientC Ménart, P Duhaut, O Attali, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 18, 1998
Levels of prothrombin activation peptide F1+2 in patients with a bleeding tendencyJ Ingerslev, M Holm, K Christiansen, et al.
International Journal of Laboratory Hematology|October 6, 2017
Comparison of an automated chemiluminescent assay to a manual ELISA assay for determination of von Willebrand Factor collagen binding activity on VWD plasma patients previously diagnosed through molecular analysis of VWFE Jousselme, Y Jourdy, L Rugeri, et al.
Journal of Thrombosis and Haemostasis : JTH|November 13, 2018
Performance of a recombinant fusion protein linking coagulation factor IX with recombinant albumin in one-stage clotting assaysC Horn, C Négrier, U Kalina, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 1, 1999
Safety and efficacy of three arthroscopic procedures using Holmium: Yag laser in two high-responder haemophiliacsC Ménart, J J Lalain, A Lienhart, et al.
Thrombosis and Haemostasis|August 28, 2001
A factor VIII minigene comprising the truncated intron I of factor IX highly improves the in vitro production of factor VIIIJ L Plantier, M H Rodriguez, N Enjolras, et al.
Thrombosis and Haemostasis|August 1, 1996
Combined hereditary disorders of haemophilia B Leyden (-6 G-->A) and type 1 von Willebrand diseaseG Pernod, C Vinciguerra, C Gaucher, et al.
Pageof 5