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

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Document type:: Zeitschriftenaufsatz
Author(s):: Terpolilli, Nicole A; Dolp, Reinhard; Waehner, Kai; Schwarzmaier, Susanne M; Rumbler, Elisabeth; Todorov, Boyan; Ferrari, Michel D; van den Maagdenberg, Arn MJM; Plesnila, Nikolaus
Title:: 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
Journal title:: eLife
Year:: 2022
Journal volume:: 11
Fulltext / DOI:: doi:10.7554/elife.74923
Publisher:: eLife Sciences Publications, Ltd
E-ISSN:: 2050-084X
Date of publication:: 03.03.2022
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