Elsebet Østergaard

Medicine & Life Sciences

1. 3-Methylglutaconic Aciduria 16%
2. Acyl-CoA Dehydrogenase 28%
3. Age of Onset 19%
4. Albinism 27%
5. Autism Spectrum Disorder 18%
6. Autosomal Recessive 48 Deafness 20%
7. Brain Diseases 27%
8. Capsicum 19%
9. Cataract 25%
10. Cell Nucleus Division 26%
11. Cytochrome-c Oxidase Deficiency 30%
12. Dental Plaque 23%
13. Electron Transport 30%
14. Fibroblasts 15%
15. Gene Deletion 20%
16. Genes 36%
17. Genetic Association Studies 40%
18. Genetic Counseling 32%
19. Hearing Loss 25%
20. Heterozygote 16%
21. human NDUFAF2 protein 15%
22. Intellectual Disability 16%
23. Labor Presentation 28%
24. Leigh Disease 26%
25. Leukoencephalopathies 23%
26. Maternal Inheritance 22%
27. Melanocytes 20%
28. Methylation 16%
29. Methylmalonic acidemia 29%
30. Missense Mutation 26%
31. Mitochondrial Diseases 36%
32. Mitochondrial DNA 49%
33. Mitochondrial Proteins 17%
34. Molecular Biology 29%
35. Multicenter Studies 15%
36. Muscle Hypotonia 16%
37. Muscles 18%
38. Mutation 100%
39. Myoglobinuria 27%
40. Nuclear Proteins 18%
41. Oxidoreductases 16%
42. Pelizaeus-Merzbacher Disease 22%
43. Phenotype 58%
44. Renal Insufficiency 15%
45. Riboflavin Deficiency 30%
46. RNA, Transfer, Met 27%
47. Seizures 20%
48. Succinate-CoA Ligases 75%
49. Transgenic Mice 16%
50. Usher Syndromes 27%