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

Benutzer: Gast

Titel:: 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
Dokumenttyp:: Zeitschriftenaufsatz
Autor(en):: Terpolilli, Nicole A; Dolp, Reinhard; Waehner, Kai; Schwarzmaier, Susanne M; Rumbler, Elisabeth; Todorov, Boyan; Ferrari, Michel D; van den Maagdenberg, Arn MJM; Plesnila, Nikolaus
Zeitschriftentitel:: eLife
Jahr:: 2022
Band / Volume:: 11
Volltext / DOI:: doi:10.7554/elife.74923
Verlag / Institution:: eLife Sciences Publications, Ltd
E-ISSN:: 2050-084X
Publikationsdatum:: 03.03.2022
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