Allan Meldgaard Lund

Medicin og biovidenskab

1. 2-hydroxyglutarate dehydrogenase 39%
2. 2-Hydroxyglutaricaciduria 17%
3. acylcarnitine 39%
4. Alleles 25%
5. Carnitine 35%
6. Cysteamine 28%
7. Cystinosis 30%
8. Denmark 83%
9. Dermatan Sulfate 27%
10. Disaccharides 25%
11. Fatty Acids 18%
12. Fertility 18%
13. Fishes 18%
14. Genes 32%
15. glutaconic acid 39%
16. Glutaric Acidemia I 64%
17. Glutaryl-CoA Dehydrogenase 36%
18. Greenland 29%
19. Growth Charts 28%
20. Heparitin Sulfate 24%
21. hydroxide ion 22%
22. Inborn Errors Metabolism 23%
23. Inborn Genetic Diseases 18%
24. Isovaleric acidemia 35%
25. Kidney Transplantation 18%
26. Leucine 20%
27. Ligases 21%
28. Marfan Syndrome 50%
29. Medium chain acyl CoA dehydrogenase deficiency 32%
30. Metachromatic Leukodystrophy 29%
31. Miller-McKusick-Malvaux-Syndrome (3M Syndrome) 38%
32. Mucopolysaccharidosis I 32%
33. Mucopolysaccharidosis II 59%
34. Mucopolysaccharidosis III 31%
35. Mutation 68%
36. N-acetylaspartate 25%
37. N-Methyl-D-Aspartate Receptors 19%
38. Neonatal Screening 100%
39. Newborn Infant 33%
40. Nuchal Translucency Measurement 27%
41. Odorants 20%
42. Osteogenesis Imperfecta 52%
43. Phenotype 32%
44. Physiologic Monitoring 20%
45. Protein-Restricted Diet 25%
46. Rare Diseases 19%
47. Receptor, Fibroblast Growth Factor, Type 3 30%
48. Systemic carnitine deficiency 44%
49. Transferases 20%
50. Trimethylaminuria 36%