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2. Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

3. Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

5. Multicenter evaluation of light transmission platelet aggregation reagents: communication from the ISTH SSC Subcommittee on Platelet Physiology

7. Plasma levels of Complement components C5 and C9 are associated with thrombin generation

8. Explainable Artificial Neural Network for Recurrent Venous Thromboembolism Based on Plasma Proteomics

11. Plasma levels of complement components C5 and C9 are associated with thrombin generation

13. An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism

16. 92 Treatment with warfarin but not Factor Xa inhibitors, is associated with dysregulated, noncanonical, complement activation

17. Multi-center evaluation of light transmission platelet aggregation reagents: Communication from the ISTH SSC Subcommittee on Platelet Physiology

19. Single-cell analysis of megakaryopoiesis in peripheral CD34+ cells: insights into ETV6-related thrombocytopenia

20. Screening platelet function in blood donors

21. Elevated plasma Complement Factor H Regulating Protein 5 is associated with venous thromboembolism and COVID-19 severity

22. Modelling of time-to-events in an ambispective study: illustration with the analysis ofABOblood groups on venous thrombosis recurrence

23. A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant

24. Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation

25. An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism

30. A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant

32. High risk of long-term recurrence after a first episode of venous thromboembolism during pregnancy or postpartum: the REcurrence after a PrEgnAncy related Thrombosis (REPEAT) Study

33. A Genome Wide Association Study on plasma FV levels identified PLXDC2as a new modifier of the coagulation process

34. Single-cell analysis of megakaryopoiesis in peripheral CD34+cells: insights into ETV6-related thrombocytopenia

35. A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.

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