Molecular investigations in the patients with defects in the complexes of the oxidative phosphorylation and the pyruvate dehydrogenase complex.

Medicine & Life Sciences

1. Mitochondrial DNA 100%
2. Oxidative Phosphorylation 99%
3. Mitochondrial Complex III Deficiency 86%
4. Mutation 80%
5. Mitochondrial Diseases 55%
6. Lactic Acidosis 53%
7. oligomycin sensitivity-conferring protein 45%
8. Electron Transport Complex III 44%
9. Leigh Disease 38%
10. Diffuse Cerebral Sclerosis of Schilder 38%
11. deoxyguanosine kinase 38%
12. Noninsulin-dependent diabetes mellitus with deafness 37%
13. Newborn Infant 37%
14. Genes 36%
15. Liver 34%
16. Myocardium 34%
17. Staining and Labeling 33%
18. Necrosis 32%
19. Progressive Myoclonic Epilepsy 31%
20. Native Polyacrylamide Gel Electrophoresis 30%
21. Pyruvate Dehydrogenase Complex 30%
22. Electron Transport 29%
23. Transfer RNA 28%
24. Muscles 28%
25. Point Mutation 28%
26. Liver Failure 26%
27. Adrenal Medulla 26%
28. Gels 25%
29. MELAS Syndrome 25%
30. polyacrylamide gels 25%
31. Hepatomegaly 24%
32. Respiratory Insufficiency 24%
33. Sequence Deletion 23%
34. Brain Diseases 23%
35. Cardiomegaly 22%
36. Adrenal Glands 22%
37. Iron 21%
38. Thalamus 20%
39. Parturition 19%
40. Abdominal Pain 18%
41. Vomiting 17%
42. Autopsy 17%
43. ubiquinol 17%
44. Yeasts 16%
45. Skeletal Muscle 16%
46. Mitochondrial Encephalomyopathies 16%
47. X-Rays 16%
48. Myocardial Infarction 15%
49. Hypoglycemia 15%
50. Phenotype 14%
51. Medical Genetics 14%
52. Fungal Proteins 12%
53. Enzymes 12%
54. Belgium 12%
55. Proteins 11%
56. Fibroblasts 11%
57. Finnish lethal neonatal metabolic syndrome 11%
58. Deoxyribonucleosides 10%
59. Dystonia 9%
60. Missense Mutation 9%
61. Oxidoreductases 9%
62. Child 9%
63. Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult 8%
64. Biopsy 8%
65. Muscle Hypotonia 8%
66. Triglycerides 8%
67. Terminator Codon 8%
68. Hyperlactatemia 8%
69. University Hospitals 8%
70. Adenosine Triphosphate 8%
71. purine 7%
72. Viverridae 7%
73. Hepatic Insufficiency 7%
74. Electron Transport Complex I 7%
75. Gastroesophageal Reflux 7%
76. Inferior Colliculi 6%
77. Myoclonic dystonia 6%
78. Pediatrics 6%
79. Mitochondrial Dynamics 6%
80. Liver Mitochondrion 6%
81. Leukocytes 6%
82. Ketosis 6%
83. Glucose 6%
84. Mitochondria 6%
85. Sulfur 6%
86. Leber's Hereditary Optic Atrophy 6%
87. Static Electricity 6%
88. Electron Transport Complex IV 6%
89. Cytochromes 5%
90. Mitochondrial Proteins 5%
91. Neuropathology 5%
92. Exons 5%
93. Mitochondrial Membranes 5%
94. Cytochromes c 5%
95. Tryptophan 5%
96. Migraine with Aura 5%
97. Glucagon 5%
98. Eukaryota 5%
99. Protons 5%
100. Parents 5%
101. Bile 5%
102. Brain 5%
103. Corpus Striatum 5%