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2. Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants.

3. Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

8. Recording, analysis, and interpretation of spreading depolarizations in neurointensive care: Review and recommendations of the COSBID research group

9. CaV2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury

10. Author response: CaV2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury

18. Epigenetic mechanisms in migraine: a promising avenue?

19. Functional crosstalk in culture between macrophages and trigeminal sensory neurons of a mouse genetic model of migraine

20. Analysis of shared heritability in common disorders of the brain

22. Lipid rafts control P2X3 receptor distribution and function in trigeminal sensory neurons of a transgenic migraine mouse model

23. Familial hemiplegic migraine CaV2.1 channel mutation R192Q enhances ATP-gated P2X3 receptor activity of mouse sensory ganglion neurons mediating trigeminal pain

24. Migraine without aura: genome-wide association analysis identifies several novel susceptibility

26. Caffeine does not affect susceptibility to cortical spreading depolarization in mice

31. Recording, analysis, and interpretation of spreading depolarizations in neurointensive care: Review and recommendations of the COSBID research group

35. Spreading depolarizations increase delayed brain injury in a rat model of subarachnoid hemorrhage

36. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

37. Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set

38. Cluster headache and the hypocretin receptor 2 reconsidered: A genetic association study and meta-analysis

39. Two novel SCN1A mutations identified in families with familial hemiplegic migraine

43. Migraine is not associated with enhanced atherosclerosis

49. Recent findings in headache genetics

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