35 results on '"Ibrahim-Kosta, Manal"'
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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
4. Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design
5. Multicenter evaluation of light transmission platelet aggregation reagents: communication from the ISTH SSC Subcommittee on Platelet Physiology
6. Single-cell analysis of megakaryopoiesis in peripheral CD34+ cells: insights into ETV6-related thrombocytopenia
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
9. Severe thrombophilia in a factor V‐deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)
10. Clinical validation of immunoassay HemosIL® AcuStar HIT-IgG (PF4-H) in the diagnosis of Heparin-induced thrombocytopenia
11. Plasma levels of complement components C5 and C9 are associated with thrombin generation
12. High prevalence of mutations in perilipin 1 in patients with precocious acute coronary syndrome
13. An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism
14. A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process
15. Explainable Artificial Neural Network for Recurrent Venous Thromboembolism Based on Plasma Proteomics
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
18. Additional file 1 of Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design
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
26. Laboratory Techniques Used to Diagnose Constitutional Platelet Dysfunction
27. ABO blood group, glycosyltransferase activity and risk of venous thromboembolism
28. Use of Sysmex XN‐10 red blood cell parameters for screening of hereditary red blood cell diseases and iron deficiency anaemia
29. Ethnicity and Haemostasis: Challenge in the genomics era
30. A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
31. Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis
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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