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Y Sultan

Showing results (131-140 of 186) with videos related to

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The Journal of the Egyptian Public Health Association|January 16, 2007
Comparative study on different recent diagnostic and therapeutic regimens in acute typhoid feverM F Abdel Wahab, I M el-Gindy, Y Sultan, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1992
Natural antibodies to factor VIII (anti-hemophilic factor) in healthy individualsM Algiman, G Dietrich, U E Nydegger, et al.
Lancet (London, England)|April 29, 1995
Weight gain in infancy and cancer of the ovaryD J Barker, P D Winter, C Osmond, et al.
Thrombosis and Haemostasis|October 30, 1985
Identification and cellular localization of plasminogen activators from human glomeruliE Angles-Cano, E Rondeau, F Delarue, et al.
Journal of Biomedical Materials Research|April 1, 1993
Human umbilical vein endothelial cell culture on heparin-like microcarriersM Najab-Benhayoun, H Serne, M Jozefowicz, et al.
Blood|October 1, 1985
Production of monoclonal antibodies to the high fibrin-affinity, tissue-type plasminogen activator of human plasma. Demonstration of its endothelial origin by immunolocalizationE Angles-Cano, A Balaton, B Le Bonniec, et al.
Vox Sanguinis|January 1, 1987
The role of HIV infectivity and composition of factor VIII concentrates on the immunity of haemophiliacs positive for HIV antibodiesJ P Allain, D Frommel, C Bosser, et al.
Thrombosis Research|July 1, 1990
High total and free protein S in patients with acute deep vein thrombosisP Toulon, S Gandrille, J F Vitoux, et al.
Journal of Chromatography. B, Biomedical Applications|February 3, 1995
Synthetic sorbents for removal of factor VIII inhibitors from haemophilic A plasmaL Dahri, C Boisson-Vidal, V Regnault, et al.
Pathologie-Biologie|November 1, 1974
Dominant inherited familial factor VIII deficiency (Von Willebrand disease) associated with thrombocytopathic thrombocytopaenia. (Biologic and genetic implications)Y Sultan, E J Bernal-Hoyos, S Levy-Toledano, et al.
Pageof 19

Showing results (131-140 of 186) with videos related to

Sort By:
Pageof 19
The Journal of the Egyptian Public Health Association|January 16, 2007
Comparative study on different recent diagnostic and therapeutic regimens in acute typhoid feverM F Abdel Wahab, I M el-Gindy, Y Sultan, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1992
Natural antibodies to factor VIII (anti-hemophilic factor) in healthy individualsM Algiman, G Dietrich, U E Nydegger, et al.
Lancet (London, England)|April 29, 1995
Weight gain in infancy and cancer of the ovaryD J Barker, P D Winter, C Osmond, et al.
Thrombosis and Haemostasis|October 30, 1985
Identification and cellular localization of plasminogen activators from human glomeruliE Angles-Cano, E Rondeau, F Delarue, et al.
Journal of Biomedical Materials Research|April 1, 1993
Human umbilical vein endothelial cell culture on heparin-like microcarriersM Najab-Benhayoun, H Serne, M Jozefowicz, et al.
Blood|October 1, 1985
Production of monoclonal antibodies to the high fibrin-affinity, tissue-type plasminogen activator of human plasma. Demonstration of its endothelial origin by immunolocalizationE Angles-Cano, A Balaton, B Le Bonniec, et al.
Vox Sanguinis|January 1, 1987
The role of HIV infectivity and composition of factor VIII concentrates on the immunity of haemophiliacs positive for HIV antibodiesJ P Allain, D Frommel, C Bosser, et al.
Thrombosis Research|July 1, 1990
High total and free protein S in patients with acute deep vein thrombosisP Toulon, S Gandrille, J F Vitoux, et al.
Journal of Chromatography. B, Biomedical Applications|February 3, 1995
Synthetic sorbents for removal of factor VIII inhibitors from haemophilic A plasmaL Dahri, C Boisson-Vidal, V Regnault, et al.
Pathologie-Biologie|November 1, 1974
Dominant inherited familial factor VIII deficiency (Von Willebrand disease) associated with thrombocytopathic thrombocytopaenia. (Biologic and genetic implications)Y Sultan, E J Bernal-Hoyos, S Levy-Toledano, et al.
Pageof 19