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Thrombosis Research|May 24, 2005
Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domainKeren Borensztajn, Ouerdia Chafa, Bernard Le Bonniec, et al.
British Journal of Haematology|March 29, 2002
Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesisKeren Borensztajn, Ouerdia Chafa, Martine Alhenc-Gelas, et al.
European Journal of Haematology|March 30, 2007
Recurrence of a Phe31Ser mutation in the Gla domain of blood coagulation factor X, in unrelated Algerian families: a founder effect?Sepideh Akhavan, Ouerdia Chafa, Fatou Nsoure Obame, et al.
Cardiovascular Research|April 21, 2012
Tie2-dependent knockout of α6 integrin subunit in mice reduces post-ischaemic angiogenesisClaire Bouvard, Adèle De Arcangelis, Blandine Dizier, et al.
Annales De Biologie Clinique|October 23, 2014
[Thrombopathy induced by selective serotonin reuptake inhibitors: a case report]Mehdi Ben Said, Laurence Amar, David Smadja, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 29, 2010
alpha6-integrin subunit plays a major role in the proangiogenic properties of endothelial progenitor cellsClaire Bouvard, Benjamin Gafsou, Blandine Dizier, et al.
Annales De Biologie Clinique|December 18, 2013
[Accreditation of automated complete blood count by the LH750 Analyzer (Beckman Coulter) in Georges Pompidou Hospital (Paris, France)]Sylvain Robinet, Pierre Lemaire, Gauthier Louis, et al.
International Journal of Cardiology|August 10, 2013
Evaluation of recombinant activated factor VII, prothrombin complex concentrate, and fibrinogen concentrate to reverse apixaban in a rabbit model of bleeding and thrombosisAnne-Céline Martin, Bernard Le Bonniec, Anne-Marie Fischer, et al.
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