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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Bibliographische Detailangaben
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Society for Clinical Investigation 2008
Schlagworte:
Research Article
Online Zugang: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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