Aida Inbal

Medicine & Life Sciences

1. Factor XIII 100%
2. von Willebrand Factor 69%
3. Blood Platelets 43%
4. Factor XIII Deficiency 41%
5. Type 2 von Willebrand Disease 38%
6. von Willebrand Diseases 37%
7. AR545C 31%
8. Habitual Abortion 25%
9. Mutation 23%
10. factor V Leiden 22%
11. Thrombophilia 21%
12. Myopathy with lactic acidosis and sideroblastic anemia 20%
13. S-nitroso-AR545C 20%
14. Blood Coagulation Factors 20%
15. diethoxyphosphoryloxymethyl butanoate 20%
16. Endothelial Cells 20%
17. Fibrinogen 18%
18. Hemorrhage 17%
19. factor XIII subunit A 17%
20. Thrombosis 16%
21. Pregnancy 16%
22. Methylenetetrahydrofolate Reductase (NADPH2) 15%
23. Type 1 von Willebrand Disease 15%
24. Platelet Membrane Glycoproteins 15%
25. Histone Deacetylase Inhibitors 14%
26. Platelet Aggregation 13%
27. Factor XIIIa 13%
28. Fibrin 12%
29. Platelet Glycoprotein GPIb-IX Complex 12%
30. Missense Mutation 12%
31. Genes 12%
32. Protein Disulfide-Isomerases 12%
33. Antiphospholipid Antibodies 11%
34. Live Birth 11%
35. Thrombin 11%
36. Vascular Endothelial Growth Factor Receptor-2 11%
37. Sideroblastic Anemia 11%
38. Pharmacokinetics 11%
39. Birth Rate 11%
40. Ristocetin 10%
41. factor VIII-von Willebrand factor concentrate 8Y 10%
42. Alleles 10%
43. Thrombospondin 1 10%
44. Hereditary Thrombophilia 10%
45. Lymphoma 9%
46. Leukemia, Myelogenous, Chronic, BCR-ABL Positive 9%
47. Thrombasthenia 9%
48. Myelodysplastic Syndromes 9%
49. Thromboplastin 9%
50. BAT monoclonal antibody 9%