M.J. Van Schooneveld

Medicine & Life Sciences

1. Retinal Dystrophies 100%
2. Retinitis Pigmentosa 78%
3. Visual Acuity 78%
4. Cone-Rod Dystrophies 47%
5. Phenotype 45%
6. Visual Fields 37%
7. Mutation 34%
8. Retinitis Pigmentosa 12 32%
9. Eye 32%
10. Optical Coherence Tomography 32%
11. Age of Onset 27%
12. Choroideremia 26%
13. Electroretinography 26%
14. Leber Congenital Amaurosis 26%
15. Stargardt Disease 24%
16. Usher Syndromes 24%
17. Retinoschisis 24%
18. Clinical Trials 23%
19. Natural History 23%
20. Retinal Degeneration 21%
21. Vision Disorders 20%
22. Netherlands 17%
23. Macular Degeneration 17%
24. Retinitis Pigmentosa 19 17%
25. Heterozygote 16%
26. Low Vision 16%
27. Genes 16%
28. Blindness 13%
29. Pedigree 13%
30. Cataract 12%
31. Registries 12%
32. Cohort Studies 12%
33. Retina 12%
34. Medical Records 12%
35. Ophthalmoscopy 11%
36. Observation 11%
37. Photography 10%
38. Cross-Sectional Studies 10%
39. Retrospective Studies 10%
40. Myopia 9%
41. Vertebrate Photoreceptor Cells 8%
42. Genetic Association Studies 8%
43. Exons 8%
44. Ocular Vision 7%
45. Incidence 7%
46. Diagnostic Errors 7%
47. Hearing Loss 6%
48. Retinal Pigment Epithelium 6%
49. Constriction 6%
50. Retinitis Pigmentosa 37 6%