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Neurology|January 19, 2018
Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutationNadine Pelzer, Joost Haan, Anine H Stam, et al.
Neurology|October 19, 2012
PRRT2 mutation causes benign familial infantile convulsionsBoukje de Vries, Petra M C Callenbach, Jessica T Kamphorst, et al.
Cephalalgia : an International Journal of Headache|November 16, 2014
Cluster headache and the hypocretin receptor 2 reconsidered: a genetic association study and meta-analysisClaudia M Weller, Leopoldine A Wilbrink, Jeanine J Houwing-Duistermaat, et al.
Cephalalgia : an International Journal of Headache|August 30, 2013
RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in miceBoukje de Vries, Else Eising, Ludo A M Broos, et al.
Neurology|November 12, 2017
δ-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsyAnne-Fleur van Rootselaar, Alexander J Groffen, Boukje de Vries, et al.
Cephalalgia : an International Journal of Headache|January 31, 2015
Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data setBoukje de Vries, Verneri Anttila, Tobias Freilinger, et al.
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.
Cephalalgia : an International Journal of Headache|December 10, 2015
Involvement of astrocyte and oligodendrocyte gene sets in migraineElse Eising, Christiaan de Leeuw, Josine L Min, et al.
Molecular Neurobiology|April 2, 2016
Cortical Spreading Depression Causes Unique Dysregulation of Inflammatory Pathways in a Transgenic Mouse Model of MigraineElse Eising, Reinald Shyti, Peter A C 't Hoen, et al.
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