Ulrika Kjellström

Medicin och livsvetenskap

1. Vigabatrin 100%
2. Electroretinography 84%
3. Mutation 66%
4. Retinitis Pigmentosa 52%
5. Optical Coherence Tomography 50%
6. Vertebrate Photoreceptor Cells 49%
7. Retinal Degeneration 49%
8. Phenotype 42%
9. Visual Fields 40%
10. Genes 36%
11. Myelocerebellar Disorder 32%
12. Snowflake vitreoretinal degeneration 31%
13. Eye 26%
14. Macular Degeneration 25%
15. Type 1 Stickler syndrome 23%
16. Cone-Rod Dystrophies 23%
17. Siblings 21%
18. Retinal Detachment 21%
19. Genetic Testing 20%
20. aflibercept 20%
21. Visual Field Tests 20%
22. Hearing Loss 20%
23. Visual Acuity 20%
24. Rabbits 19%
25. Newfoundland and Labrador 19%
26. Protein Kinase C-alpha 19%
27. Loss of Function Mutation 19%
28. Leukoencephalopathies 18%
29. Cataract 18%
30. Nerve Fibers 18%
31. Ataxia 17%
32. Pancytopenia 17%
33. Cilia 16%
34. Paraplegia 16%
35. Cyclic GMP 16%
36. Genetic Association Studies 14%
37. Glare 13%
38. Retinal Cone Photoreceptor Cells 12%
39. Exome 12%
40. Arm 12%
41. Child 12%
42. Tyrosine-tRNA Ligase 12%
43. Nervous System 11%
44. Congenital Nystagmus 11%
45. Retinal Rod Photoreceptor Cells 10%
46. Optic Disk 10%
47. Constriction 10%
48. Agenesis of Corpus Callosum 9%
49. Vimentin 9%
50. Hematologic Neoplasms 9%