Glutamate-system defects behind psychiatric manifestations in a familial hemiplegic migraine type 2 disease-mutation mouse model-Reference-Cited by-同舟云学术

Glutamate-system defects behind psychiatric manifestations in a familial hemiplegic migraine type 2 disease-mutation mouse model

Published:2016-02 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Bøttger Pernille,Glerup Simon,Gesslein Bodil,Illarionova Nina B.,Isaksen Toke J.,Heuck Anders,Clausen Bettina H.,Füchtbauer Ernst-Martin,Gramsbergen Jan B.,Gunnarson Eli,Aperia Anita,Lauritzen Martin,Lambertsen Kate L.,Nissen Poul,Lykke-Hartmann Karin

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep22047.pdf

Reference95 articles.

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3. Ferrari, M. D., Klever, R. R., Terwindt, G. M., Ayata, C. & van den Maagdenberg, A. M. Migraine pathophysiology: lessons from mouse models and human genetics. Lancet Neurol. 14, 65–80 (2015).

4. Santoro, L. et al. A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation. Cephalalgia 31, 808–819 (2011).

5. Thomsen, L. L. et al. A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria. Brain 125, 1379–1391 (2002).

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