池田 真理子

Medicine & Life Sciences

1. Walker-Warburg Syndrome 100%
2. Dystroglycans 36%
3. Genes 34%
4. Muscular Dystrophies 33%
5. Mutation 30%
6. Hereditary Nephritis 25%
7. Gestational Age 21%
8. Pediatrics 20%
9. Umbilical Cord 20%
10. Child 20%
11. Glycosylation 18%
12. Glomerulopathy with fibronectin deposits 18%
13. Mosaicism 17%
14. High-Throughput Nucleotide Sequencing 16%
15. Meiosis 15%
16. Fever 15%
17. Exons 14%
18. Alleles 14%
19. Gitelman Syndrome 14%
20. Cruciform DNA 13%
21. Mothers 13%
22. Laminin 12%
23. Proteins 12%
24. Status Epilepticus 12%
25. Brain Diseases 11%
26. Consciousness 11%
27. Newborn Infant 11%
28. Induced Pluripotent Stem Cells 11%
29. Emergencies 10%
30. Chromosome Segregation 10%
31. Febrile Seizures 10%
32. Japan 10%
33. Seizures 10%
34. Muscles 10%
35. Brain 9%
36. Anaphylaxis 9%
37. Chromosome 12p partial deletion 9%
38. Bilirubin 9%
39. Autosomal recessive distal renal tubular acidosis 8%
40. Duchenne Muscular Dystrophy 8%
41. X Chromosome Inactivation 8%
42. Glycosylphosphatidylinositol deficiency 8%
43. Nonsense Codon 8%
44. Dent Disease 8%
45. Short Interspersed Nucleotide Elements 8%
46. Congenital chloride diarrhea 7%
47. Receptors, Tumor Necrosis Factor, Member 25 7%
48. Mesenchymal Stem Cells 7%
49. Hyperbilirubinemia 7%
50. Adams Oliver syndrome 7%