Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1

Familial hemiplegic migraine type 1 (FHM1) is an autosomal dominant subtype of migraine with aura that is associated with hemiparesis. As with other types of migraine, it affects women more frequently than men. FHM1 is caused by mutations in the CACNA1A gene, which encodes the α(1A) subunit of Ca(v)...

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Bibliografiska uppgifter
Huvudupphovsmän: Eikermann-Haerter, Katharina, Dileköz, Ergin, Kudo, Chiho, Savitz, Sean I., Waeber, Christian, Baum, Michael J., Ferrari, Michel D., van den Maagdenberg, Arn M.J.M., Moskowitz, Michael A., Ayata, Cenk
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Society for Clinical Investigation 2008
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2613474/
https://ncbi.nlm.nih.gov/pubmed/19104150
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI36059
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