Allan Bayat

Medicin og biovidenskab

1. Seizures 100%
2. Epilepsy 87%
3. Neurodevelopmental Disorders 70%
4. Intellectual Disability 59%
5. Mowat-Wilson syndrome 54%
6. Phenotype 53%
7. Brain Diseases 53%
8. Glycosylphosphatidylinositols 46%
9. Genes 46%
10. AMPA Receptors 34%
11. Cerebellar Hypoplasia 32%
12. Muscle Hypotonia 30%
13. Denmark 30%
14. Genetic Testing 30%
15. Exome 28%
16. Myoclonic Epilepsy 27%
17. Status Epilepticus 26%
18. Genetic Association Studies 26%
19. Glycosylphosphatidylinositol deficiency 23%
20. Omodysplasia type 1 21%
21. Mutation 21%
22. phosphatidylinositol glycan-class A protein 20%
23. Infantile Epileptic-Dyskinetic Encephalopathy 20%
24. Trisomy 20p 20%
25. Electroencephalography 19%
26. 3C syndrome 19%
27. Neurologic Manifestations 19%
28. Generalized Epilepsy 19%
29. Coffin-Siris syndrome 17%
30. Congenital contractural arachnodactyly 17%
31. Perisylvian syndrome 17%
32. Congenital Disorders of Glycosylation 17%
33. DiGeorge Syndrome 16%
34. Epileptic Syndromes 15%
35. Pyridoxal Phosphate 15%
36. Nervous System Diseases 15%
37. Extremities 15%
38. Genotype 14%
39. Pyridoxine 14%
40. Premature Mortality 14%
41. Growth Charts 13%
42. Child 13%
43. Monosomy 13%
44. Brain 12%
45. Phenylketonurias 12%
46. Neurofibromatoses 12%
47. Flow Cytometry 12%
48. Mitochondrial Diseases 12%
49. Neurofibromatosis 1 11%
50. Population 11%