Rikke Steensbjerre Møller

Medicin og biovidenskab

1. Absence Epilepsy 5%
2. Autism Spectrum Disorder 6%
3. Autistic Disorder 5%
4. Brain 10%
5. Brain Diseases 70%
6. Chromosome 15q13.3 Microdeletion Syndrome 5%
7. Congenital Disorders of Glycosylation 6%
8. Drug Resistant Epilepsy 5%
9. Electroencephalography 14%
10. Epilepsy 100%
11. Epileptic Syndromes 14%
12. Episodic Ataxia 7%
13. Exome 8%
14. Exons 5%
15. Febrile Seizures 6%
16. Generalized Epilepsy 25%
17. Genes 29%
18. Genetic Association Studies 14%
19. Genetic Heterogeneity 5%
20. Genetic Testing 7%
21. Genotype 5%
22. Haploinsufficiency 5%
23. High-Throughput Nucleotide Sequencing 7%
24. Idiopathic Generalized Epilepsy 15%
25. Infantile Epileptic-Dyskinetic Encephalopathy 6%
26. Infantile Spasms 12%
27. Intellectual Disability 36%
28. Malformations of Cortical Development 6%
29. Microcephaly 8%
30. Movement Disorders 8%
31. Mowat-Wilson syndrome 12%
32. Muscle Hypotonia 7%
33. Mutation 40%
34. Myoclonic Epilepsy 19%
35. Neurodevelopmental Disorders 36%
36. Neuroimaging 5%
37. Partial Epilepsy 11%
38. Phenotype 33%
39. Proteins 5%
40. Rolandic Epilepsy 9%
41. Seizures 48%
42. Sleep 6%
43. Sodium Channels 8%
44. Status Epilepticus 7%
45. Whole Exome Sequencing 5%