Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
British Journal of Haematology|October 16, 1999
Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutationV Le Cam-Duchez, S Gandrille, D Trégouët, et al.
La Revue De Medecine Interne|March 21, 2009
[Anticoagulation clinics for outpatients: a 5-year experience]Y Benhamou, V Le Cam-Duchez, J-M Schneller, et al.
Journal of Thrombosis and Haemostasis : JTH|July 17, 2008
Pharmacokinetics and pharmacodynamics of a new highly secured fibrinogen concentrateC Négrier, C Rothschild, J Goudemand, et al.
Vox Sanguinis|September 2, 2016
Post-authorization safety study of Clottafact<sup>®</sup> , a triply secured fibrinogen concentrate in congenital afibrinogenemia. A prospective observational studyC Négrier, C Rothschild, J-Y Borg, et al.
Journal of Thrombosis and Haemostasis : JTH|July 13, 2012
The IgG autoimmune response in postpartum acquired hemophilia A targets mainly the A1a1 domain of FVIIIP Lapalud, T Ali, C Cayzac, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 5, 2002
Venous thromboembolism during pregnancy: a retrospective study of enoxaparin safety in 624 pregnanciesJ Lepercq, J Conard, A Borel-Derlon, et al.
La Revue De Medecine Interne|January 1, 1988
[Circulating anticoagulants excluding hemophilia. Multicenter survey undertaken under the aegis of the French National Society of Internal Medicine apropos of 207 cases]D u Lê Thi Huong, L Guillevin, J Y Borg, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 31, 2015
Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing studyF Bauduer, E de Raucourt, C Boyer-Neumann, et al.
Human Genetics|May 17, 2001
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genesM Neerman-Arbez, P de Moerloose, A Honsberger, et al.
Haematologica|June 15, 2004
Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?Muriel Giansily-Blaizot, Régis Verdier, Christine Biron-Adréani, et al.
Pageof 6