Neurology & Neurotherapeutics - NE Neuro Pediatrics Section

Medicine & Life Sciences

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