Marina Pedemonte

Medicine & Life Sciences

1. Duchenne Muscular Dystrophy 100%
2. nusinersen 86%
3. Spinal Muscular Atrophies of Childhood 69%
4. Mutation 59%
5. Muscles 53%
6. Spinal Muscular Atrophy 49%
7. Child 40%
8. Muscular Diseases 35%
9. Noninvasive Ventilation 34%
10. Phenotype 32%
11. Muscular Dystrophies 29%
12. Nonsense Codon 27%
13. Myosin Heavy Chains 27%
14. Myotonia Congenita 27%
15. Cofilin 2 27%
16. Dystrophin 26%
17. Genes 23%
18. Terminator Codon 22%
19. Neurodevelopmental Disorders 21%
20. Leukodystrophy, Hypomyelinating, 5 21%
21. Muscle Hypotonia 19%
22. Biopsy 18%
23. Natural History 17%
24. Pediatrics 16%
25. Caveolin 3 14%
26. Neurology 14%
27. Neurodegenerative Diseases 14%
28. Mitochondrial DNA 13%
29. Muscle Weakness 12%
30. Exons 12%
31. Mitochondrial Diseases 12%
32. Intellectual Disability 12%
33. Skeletal Muscle 12%
34. Respiratory Muscles 11%
35. Neurologic Examination 11%
36. Nucleotides 11%
37. Ataxia 10%
38. Upper Extremity 10%
39. Walker-Warburg Syndrome 9%
40. Genetic Association Studies 9%
41. Child Development 9%
42. Limb-Girdle Muscular Dystrophies 9%
43. Hospitalization 9%
44. Cerebellar Hypoplasia 9%
45. Young Adult 9%
46. protein O-mannose beta-1,2-N-acetylglucosaminyltransferase 8%
47. Peripheral Nervous System 8%
48. Respiratory Insufficiency 8%
49. ataluren 8%
50. Mitochondrial Myopathies 8%