水野 晴夫

Medicine & Life Sciences

1. Nephrogenic Diabetes Insipidus 100%
2. Annexin A1 98%
3. Congenital Hypothyroidism 96%
4. Mutation 94%
5. Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 94%
6. Neonatal Sepsis 87%
7. Genes 84%
8. Japan 83%
9. pregnanetriolone 60%
10. Glucocorticoids 60%
11. Type 1 Diabetes Mellitus 59%
12. Endothelin Receptor Antagonists 59%
13. Thyrotropin Receptors 58%
14. Child 58%
15. Iodides 56%
16. Insulin 51%
17. Molecular Cloning 51%
18. Castration 48%
19. Kallmann Syndrome 46%
20. Y Chromosome 44%
21. Serum 41%
22. Astrocytes 40%
23. Allan-Herndon-Dudley syndrome 40%
24. Histidine Ammonia-Lyase 39%
25. Mass Screening 39%
26. Mixed Gonadal Dysgenesis 37%
27. Pediatrics 37%
28. Thyroid Gland 37%
29. Kabuki syndrome 36%
30. Shwachman-Diamond Syndrome 36%
31. Deamino Arginine Vasopressin 36%
32. Vasopressin Receptors 36%
33. Arterial Pressure 35%
34. CHARGE Syndrome 35%
35. Dexamethasone 35%
36. Insulin Detemir 34%
37. Uridine Monophosphate 33%
38. Mason-Type Diabetes 33%
39. Adrenal Cortex 33%
40. Edaravone 33%
41. Bartter Syndrome 33%
42. Hypothyroidism 32%
43. Steroid 21-Hydroxylase 32%
44. Chickenpox Vaccine 32%
45. Mothers 31%
46. Thiazides 30%
47. Pulmonary Hypertension 30%
48. Virilism 30%
49. Aseptic Meningitis 30%
50. Polydipsia 30%