Gary Gottesman

Medicine & Life Sciences

1. Familial Hypophosphatemic Rickets 100%
2. burosumab 93%
3. Mutation 65%
4. Rickets 46%
5. Osteochondrodysplasias 40%
6. Hypophosphatasia 38%
7. Hyperostosis corticalis deformans juvenilis 35%
8. Bone and Bones 32%
9. Collagen Type I 31%
10. Alkaline Phosphatase 30%
11. Osteogenesis 25%
12. Child 25%
13. Osteosclerosis 22%
14. Untranslated Regions 22%
15. Exons 22%
16. Base Pairing 21%
17. PHEX Phosphate Regulating Neutral Endopeptidase 21%
18. Bruck syndrome 2 21%
19. Genes 20%
20. Point Mutation 20%
21. Levin type Osteogenesis imperfecta 19%
22. Metachondromatosis 18%
23. Osteoprotegerin 18%
24. Type V Osteogenesis Imperfecta 17%
25. Infantile Hypophosphatasia 17%
26. Sp7 Transcription Factor 17%
27. Hajdu-Cheney Syndrome 16%
28. Arterial calcification of infancy 16%
29. Anoctamins 16%
30. Exome 16%
31. Melorheostosis 16%
32. Type IV Osteogenesis Imperfecta 16%
33. Blau syndrome 15%
34. Sp Transcription Factors 15%
35. Pyridoxal Phosphate 15%
36. Low Density Lipoprotein Receptor-Related Protein-6 15%
37. Serum 15%
38. Low Density Lipoprotein Receptor-Related Protein-5 15%
39. Collagen 15%
40. Pediatrics 14%
41. Mucopolysaccharidoses 14%
42. Mucopolysaccharidosis IV 14%
43. Monoclonal Antibodies 14%
44. Vitamin B 6 Deficiency 14%
45. Chromosome Painting 14%
46. Therapeutics 14%
47. Plexiform Neurofibroma 14%
48. Progeria 13%
49. Etidronic Acid 13%
50. Osteoblasts 13%