Zobrazeno 1 - 3
of 3
pro vyhledávání: '"A. C. Fasquel"'
Autor:
Jes Olesen, Kari Stefansson, A. C. Fasquel, E Oestergaard, Hreinn Stefansson, Asgeir Björnsson, Jeff Gulcher, LL Thomsen
Publikováno v:
Cephalalgia. 28:914-921
The aim of this study was to investigate the involvement of the CACNA1A and ATP1A2 gene in a population-based sample of sporadic hemiplegic migraine (SHM). Patients with SHM ( n = 105) were identified in a nationwide search in the Danish population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6348382b1d5fd9d054209acb92098c44
https://doi.org/10.1111/j.1468-2982.2008.01599.x
https://doi.org/10.1111/j.1468-2982.2008.01599.x
Autor:
Mike Frigge, H. Petursson, LL Thomsen, M. Stefansson, Hreinn Stefansson, Asgeir Björnsson, Kari Stefansson, R. M. Jensen, Jes Olesen, M. Kirchmann, A. C. Fasquel, Jeff Gulcher, Augustine Kong
Publikováno v:
Brain : a journal of neurology. 130(Pt 2)
Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura and transient hemiplegia. FHM mutations are known in three genes, the CACNA1A (FHM1) gene, the ATP1A2 (FHM2) and the SCN1A (FHM3) gene and seem to have an autosomal-dominant m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a49e7055639179d4958f00c645af85f
https://pubmed.ncbi.nlm.nih.gov/17235123
https://pubmed.ncbi.nlm.nih.gov/17235123
Autor:
L. L. Thomsen, M. Kirchmann, A. Bjornsson, H. Stefansson, R. M. Jensen, A. C. Fasquel, H. Petursson, M. Stefansson, M. L. Frigge, A. Kong, J. Gulcher, K. Stefansson, J. Olesen
Publikováno v:
Brain: A Journal of Neurology; Feb2007, Vol. 130 Issue 2, p346-356, 11p