Neurology & Neurotherapeutics - NE Neuro Pediatrics Section

Medicine & Life Sciences

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