Medicine & Life Sciences

1. Muscular Diseases 100%
2. Congenital Myasthenic Syndromes 87%
3. Mutation 82%
4. Cholinergic Receptors 68%
5. Muscles 55%
6. Distal Myopathies 36%
7. Muscle Weakness 35%
8. Inclusion Body Myositis 28%
9. Genes 25%
10. Muscular Dystrophies 24%
11. Myotonic Dystrophy 22%
12. Mitochondrial Diseases 22%
13. Biopsy 21%
14. Phenotype 20%
15. Myotonia Congenita 18%
16. Mitochondrial DNA 18%
17. Myasthenia Gravis 17%
18. peripheral membrane protein 43K 16%
19. Rhabdomyolysis 15%
20. Kinetics 15%
21. Anoctamins 14%
22. Valosin Containing Protein 13%
23. Nemaline Myopathies 13%
24. Creatine Kinase 13%
25. Vacuolar myopathy 13%
26. Missense Mutation 13%
27. Vacuoles 12%
28. Atrophy 12%
29. Myalgia 12%
30. Amyloid 12%
31. 1 Rippling muscle disease 12%
32. Congenital Structural Myopathies 12%
33. Chronic Progressive External Ophthalmoplegia 11%
34. Amyloidosis 11%
35. Minicore Myopathy with External Ophthalmoplegia 11%
36. Electromyography 10%
37. Facioscapulohumeral Muscular Dystrophy 10%
38. Tremor 10%
39. Acetylcholine 9%
40. Camptocormia 9%
41. Extremities 9%
42. Myotonia 9%
43. High-Throughput Nucleotide Sequencing 9%
44. Limb-Girdle Muscular Dystrophies 9%
45. Optic Atrophy 9%
46. Mitochondrial Myopathies 9%
47. Fathers 9%
48. Skeletal Muscle 8%
49. Nonaka type Distal myopathy 8%
50. Psychologic Desensitization 8%