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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2008
Assuntos:
Research Article
Acesso em linha: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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