Andreas Hillarp

Medicin och livsvetenskap

1. Complement C4b-Binding Protein 100%
2. Protein S 69%
3. Activated Protein C Resistance 63%
4. Factor V 40%
5. Prothrombin 40%
6. Factor VIII 39%
7. Prothrombin Time 34%
8. von Willebrand Factor 34%
9. Venous Thrombosis 33%
10. human C4BPA protein 32%
11. von Willebrand Diseases 32%
12. Anticoagulants 30%
13. Protein C 29%
14. Hemophilia A 29%
15. Protein S Deficiency 29%
16. Mutation 28%
17. Factor Xa Inhibitors 26%
18. Thrombosis 26%
19. Serum Amyloid P-Component 25%
20. Retinal Vein Occlusion 24%
21. Antithrombins 22%
22. factor V Leiden 20%
23. Partial Thromboplastin Time 19%
24. Hemorrhage 18%
25. Genes 18%
26. Lupus Coagulation Inhibitor 18%
27. Protein Binding 17%
28. International Normalized Ratio 16%
29. Aspirin 16%
30. Venous Thromboembolism 16%
31. Thrombophilia 16%
32. Dabigatran 15%
33. Alleles 14%
34. Hemostasis 14%
35. Blood Platelets 14%
36. Proteins 13%
37. Autoantibodies 13%
38. Complement Factor H 12%
39. Thrombotic Thrombocytopenic Purpura 12%
40. Factor IX 12%
41. fibrin fragment D 11%
42. Antibodies 11%
43. Semen 11%
44. Warfarin 11%
45. Hemostatics 11%
46. Molecular Cloning 11%
47. Rivaroxaban 10%
48. Atypical Hemolytic Uremic Syndrome 10%
49. Binding Sites 10%
50. Calibration 10%