Neurology & Neurotherapeutics - NE Neuro Pediatrics Section

Medicine & Life Sciences

1. Glucose 100%
2. Brain 90%
3. Glut1 Deficiency Syndrome 84%
4. Facilitative Glucose Transport Proteins 83%
5. Mutation 79%
6. Epilepsy 65%
7. Seizures 59%
8. Citric Acid Cycle 52%
9. Autistic Disorder 47%
10. Glucose Transporter Type 1 42%
11. Ketogenic Diet 39%
12. Auditory Cortex 39%
13. Acetyl Coenzyme A 35%
14. Phenotype 33%
15. Pyruvic Acid 33%
16. triheptanoin 33%
17. Mitochondrial DNA 32%
18. Nervous System Diseases 32%
19. Mitochondrial Diseases 32%
20. Genes 31%
21. Cholinergic Receptors 30%
22. Pyruvate Dehydrogenase Complex Deficiency Disease 29%
23. Cysteine 29%
24. Ataxia 28%
25. MELAS Syndrome 28%
26. methanethiosulfonate 27%
27. Child 27%
28. Oxidoreductases 25%
29. Microcephaly 25%
30. Lactic Acidosis 24%
31. Neurons 23%
32. Autism Spectrum Disorder 23%
33. Neurosciences 22%
34. Oocytes 22%
35. Glycine 22%
36. Molecular Biology 21%
37. Therapeutics 21%
38. Genetic Association Studies 21%
39. 3-O-Methylglucose 21%
40. Magnetic Resonance Spectroscopy 20%
41. Glutamic Acid 20%
42. Blood-Brain Barrier 20%
43. Brain Neoplasms 19%
44. Intellectual Disability 18%
45. Voltage-Gated Potassium Channels 18%
46. Learning 18%
47. Social Behavior 17%
48. Mental Disorders 17%
49. Brain Diseases 17%
50. Chorea 17%
51. Static Electricity 16%
52. Glycolysis 16%
53. Membranes 15%
54. Myopathic Form Mitochondrial DNA Depletion Syndrome 15%
55. Epileptic Syndromes 15%
56. Blood Glucose 15%
57. Glutamine 15%
58. Glioma 15%
59. alpha-hydroxyglutarate 15%
60. Tetraethylammonium 14%
61. Heptanoates 14%
62. Neurotransmitter Agents 14%
63. Glycogen 14%
64. Pyruvate Carboxylase 14%
65. thymidine kinase 2 14%
66. Copper 14%
67. Acetylcholine 13%
68. Glioblastoma 13%
69. Magnetic Resonance Imaging 13%
70. Cerebrovascular Circulation 13%
71. beta-hydroxyvaleric acid 13%
72. Energy Metabolism 13%
73. Haploinsufficiency 13%
74. Pyruvate Carboxylase Deficiency Disease 13%
75. Neuronal intranuclear inclusion disease 13%
76. Lactic Acid 13%
77. Neurologists 12%
78. Genetic Counseling 12%
79. Adenosine Triphosphate 12%
80. Astrocytes 12%
81. Congenital Fibrosis of the Extraocular Muscles 12%
82. Missense Mutation 12%
83. Wolman Disease 12%
84. Synaptic Transmission 12%
85. Alternating hemiplegia of childhood 12%
86. Neurology 12%
87. Nervous System 11%
88. Carbon-13 Magnetic Resonance Spectroscopy 11%
89. cupric chloride 11%
90. Autoimmune Lymphoproliferative Syndrome 11%
91. Genetic Databases 11%
92. Pyruvate Dehydrogenase Complex 11%
93. Electroencephalography 11%
94. oligomycin sensitivity-conferring protein 11%
95. Water 11%
96. Long-Term Synaptic Depression 11%
97. Mitochondrial Proton-Translocating ATPases 11%
98. Membrane Potentials 10%
99. Alzheimer Disease 10%
100. Mitochondrial Encephalomyopathies 10%