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International Journal of Laboratory Hematology|July 22, 2014
Prospective evaluation of automatized PF4/heparin immunoassays HemosIL HIT-ab (PF4-H) for the diagnosis of heparin-induced thrombocytopeniaY Jourdy, C Nougier, L Rugeri, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 27, 2016
Characterization of five associations of F8 missense mutations containing FVIII B domain mutationsY Jourdy, C Nougier, O Roualdes, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 25, 2015
Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiencyO Roualdes, C Nougier, M Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 29, 2013
The benefits of exercise for patients with haemophilia and recommendations for safe and effective physical activityC Negrier, A Seuser, A Forsyth, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|June 16, 2007
Adaptability of protein A-immunoadsorption allows temporary reduction of anti-VIII antibodies and realisation of high-risk haemorrhagic surgeryO Hequet, A Lienhart, S Jaeger, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 31, 2013
Characterization of four novel molecular changes in the promoter region of the factor VIII geneC Nougier, O Roualdes, M Fretigny, et al.
British Journal of Anaesthesia|April 29, 2008
Evaluation of rotation thrombelastography for the diagnosis of hyperfibrinolysis in trauma patientsA Levrat, A Gros, L Rugeri, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 17, 2013
The first recombinant FVIII produced in human cells--an update on its clinical development programmeL A Valentino, C Negrier, G Kohla, et al.
Thrombosis and Haemostasis|September 1, 1995
Molecular study of Glanzmann thrombasthenia in 3 patients issued from 2 different familiesC Vinciguerra, M C Trzeciak, N Philippe, et al.
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