Klaus Brusgaard

Medicin og biovidenskab

1. Congenital Hyperinsulinism 100%
2. Hereditary Hemorrhagic Telangiectasia 50%
3. Mutation 50%
4. Hypoglycemia 36%
5. Genes 24%
6. Phenotype 18%
7. Polycystic Ovary Syndrome 14%
8. Insulin 14%
9. Genetic Testing 12%
10. Diazoxide 11%
11. Insulin Secretion 11%
12. Skeletal Muscle Fibers 11%
13. Islets of Langerhans 10%
14. Hypophosphatemic Rickets 10%
15. Glucose 10%
16. Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia 10%
17. Octreotide 9%
18. Child 9%
19. Glucokinase 8%
20. Beckwith-Wiedemann Syndrome 8%
21. Germ-Line Mutation 7%
22. Genetic Association Studies 7%
23. Arteriovenous Malformations 7%
24. Pancreatitis 7%
25. Cohort Studies 6%
26. Adenosine Triphosphate 6%
27. Pancreatic Neoplasms 6%
28. KATP Channels 6%
29. Familial Hypophosphatemic Rickets 6%
30. Gene Expression 6%
31. Glycogen Storage Disease Type Ix 6%
32. Familial Hypobetalipoproteinemia 5%
33. Secretory Pathway 5%
34. Blood Glucose 5%
35. 1,4,7,10-tetraazacyclododecane- 1,4,7,10-tetraacetic acid 5%
36. Endoglin 5%
37. Kabuki syndrome 5%
38. Insulin Resistance 5%
39. Hirsutism 5%
40. Peutz-Jeghers Syndrome 5%
41. Polyps 5%
42. Genotype 5%
43. 25-Hydroxyvitamin D3 1-alpha-Hydroxylase 5%
44. Kazal Pancreatic Trypsin Inhibitor 5%
45. Dihydroxyphenylalanine 5%
46. Type 2 Diabetes Mellitus 5%
47. Single Nucleotide Polymorphism 5%
48. Mosaicism 5%
49. Bone and Bones 5%
50. Vitamin D 5%