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J-M Freyssinet

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Nouvelle Revue Francaise D'Hematologie|January 1, 1991
Anti-phospholipid auto-antibodies and thrombosisJ M Freyssinet, L Grunebaum, J Goetz, et al.
Blood|February 15, 1996
Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorderF Toti, N Satta, E Fressinaud, et al.
La Revue De Medecine Interne|January 1, 1991
[Congenital deficiencies of natural anticoagulant systems responsible for recurrent thromboembolism]L Grunebaum, M L Wiesel, J M Freyssinet, et al.
Presse Medicale (Paris, France : 1983)|July 2, 1988
[Protein C: importance of its assay in pathology]M L Wiesel, L Grunebaum, J M Freyssinet, et al.
The Biochemical Journal|March 15, 1996
Oyxsterols induce membrane procoagulant activity in monocytic THP-1 cellsK Aupeix, F Toti, N Satta, et al.
Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
Eptifibatide-induced thrombocytopenia and circulating procoagulant platelet-derived microparticles in a patient with acute coronary syndromeO Morel, L Jesel, M Chauvin, et al.
Platelets|March 20, 2010
Scott syndrome: an inherited defect of the procoagulant activity of plateletsN Satta, F Toti, E Fressinaud, et al.
Clinical and Experimental Immunology|January 1, 1996
Detection of bilayer phospholipid-binding antibodies using flow cytometryV Eschwège, I Laude, F Toti, et al.
Journal of Molecular Biology|February 11, 1994
Formation of two-dimensional arrays of annexin V on phosphatidylserine-containing liposomesC Pigault, A Follenius-Wund, M Schmutz, et al.
The Biochemical Journal|February 1, 1978
Protein-protein interactions in blood clotting. The use of polarization of fluorescence to measure the dissociation of plasma factor XIIIaJ M Freyssinet, B A Lewis, J J Holbrook, et al.
Pageof 10

Showing results (31-40 of 100) with videos related to

Sort By:
Pageof 10
Nouvelle Revue Francaise D'Hematologie|January 1, 1991
Anti-phospholipid auto-antibodies and thrombosisJ M Freyssinet, L Grunebaum, J Goetz, et al.
Blood|February 15, 1996
Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorderF Toti, N Satta, E Fressinaud, et al.
La Revue De Medecine Interne|January 1, 1991
[Congenital deficiencies of natural anticoagulant systems responsible for recurrent thromboembolism]L Grunebaum, M L Wiesel, J M Freyssinet, et al.
Presse Medicale (Paris, France : 1983)|July 2, 1988
[Protein C: importance of its assay in pathology]M L Wiesel, L Grunebaum, J M Freyssinet, et al.
The Biochemical Journal|March 15, 1996
Oyxsterols induce membrane procoagulant activity in monocytic THP-1 cellsK Aupeix, F Toti, N Satta, et al.
Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
Eptifibatide-induced thrombocytopenia and circulating procoagulant platelet-derived microparticles in a patient with acute coronary syndromeO Morel, L Jesel, M Chauvin, et al.
Platelets|March 20, 2010
Scott syndrome: an inherited defect of the procoagulant activity of plateletsN Satta, F Toti, E Fressinaud, et al.
Clinical and Experimental Immunology|January 1, 1996
Detection of bilayer phospholipid-binding antibodies using flow cytometryV Eschwège, I Laude, F Toti, et al.
Journal of Molecular Biology|February 11, 1994
Formation of two-dimensional arrays of annexin V on phosphatidylserine-containing liposomesC Pigault, A Follenius-Wund, M Schmutz, et al.
The Biochemical Journal|February 1, 1978
Protein-protein interactions in blood clotting. The use of polarization of fluorescence to measure the dissociation of plasma factor XIIIaJ M Freyssinet, B A Lewis, J J Holbrook, et al.
Pageof 10