M.J. Van Schooneveld

Medicine & Life Sciences

1. Retinal Dystrophies 100%
2. Retinitis Pigmentosa 64%
3. Visual Acuity 63%
4. Cone-Rod Dystrophies 38%
5. Phenotype 36%
6. Visual Fields 30%
7. Mutation 28%
8. Retinitis Pigmentosa 12 26%
9. Eye 26%
10. Optical Coherence Tomography 26%
11. Age of Onset 22%
12. Choroideremia 21%
13. Electroretinography 21%
14. Clinical Trials 21%
15. Leber Congenital Amaurosis 21%
16. Stargardt Disease 20%
17. Usher Syndromes 19%
18. Retinoschisis 19%
19. Natural History 18%
20. Retinal Degeneration 17%
21. Vision Disorders 17%
22. Netherlands 14%
23. Macular Degeneration 14%
24. Retinitis Pigmentosa 19 13%
25. Heterozygote 13%
26. Low Vision 13%
27. Genes 13%
28. Longitudinal Studies 12%
29. Ocular Vision 11%
30. Blindness 10%
31. Pedigree 10%
32. Cataract 10%
33. Registries 10%
34. Cohort Studies 10%
35. Retina 9%
36. Medical Records 9%
37. Ophthalmoscopy 9%
38. Observation 9%
39. Photography 8%
40. Cross-Sectional Studies 8%
41. Quality of Life 8%
42. Retrospective Studies 8%
43. Myopia 7%
44. Vertebrate Photoreceptor Cells 7%
45. Genetic Association Studies 7%
46. Exons 6%
47. Incidence 6%
48. Diagnostic Errors 6%
49. Disease Progression 6%
50. Hearing Loss 5%