Showing results (11-20 of 21) with videos related to
Sort By:
Pageof 3
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.Cephalalgia : an International Journal of Headache|April 8, 2014
Two novel SCN1A mutations identified in families with familial hemiplegic migraineClaudia M Weller, Nadine Pelzer, Boukje de Vries, et al.Journal of Human Genetics|October 24, 2007
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraineMaria-José Castro, Anine H Stam, Carolina Lemos, et al.Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.European Journal of Human Genetics : EJHG|May 3, 2007
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraineKaate R J Vanmolkot, Anine H Stam, Ashok Raman, et al.Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.Nature Genetics|August 31, 2010
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1Verneri Anttila, Hreinn Stefansson, Mikko Kallela, et al.Nature Genetics|June 25, 2013
Genome-wide meta-analysis identifies new susceptibility loci for migraineVerneri Anttila, Bendik S Winsvold, Padhraig Gormley, et al.Pageof 3