John Vissing

Medicine & Life Sciences

1. Muscles 100%
2. Limb-Girdle Muscular Dystrophies 56%
3. Exercise 55%
4. Mutation 52%
5. Glycogen Storage Disease Type V 39%
6. Muscular Diseases 37%
7. Myotonia Congenita 32%
8. Phenotype 30%
9. Duchenne Muscular Dystrophy 30%
10. Muscle Strength 30%
11. Mitochondrial Myopathies 28%
12. Skeletal Muscle 26%
13. X-Linked Bulbo-Spinal Atrophy 25%
14. Glycogen Storage Disease Type II 25%
15. Myotonic Dystrophy 25%
16. Fats 24%
17. Muscle Weakness 23%
18. Mitochondrial DNA 23%
19. Limb-girdle muscular dystrophy type 2A 23%
20. Glycogen 22%
21. Muscular Dystrophy, Limb-Girdle, Type 2I 20%
22. Glycogen Storage Disease 19%
23. Facioscapulohumeral Muscular Dystrophy 18%
24. Muscular Dystrophies 18%
25. Genes 17%
26. Oculopharyngeal Muscular Dystrophy 15%
27. Glycogen Storage Disease XIV 15%
28. Myotonia 15%
29. Creatine Kinase 15%
30. Late Onset Disorders 15%