Showing results (1-10 of 13) with videos related to
Sort By:
Pageof 2
Nederlands Tijdschrift Voor Geneeskunde|October 22, 2004
[From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene]E E Kors, K R J Vanmolkot, J Haan, et al.Neuropediatrics|November 10, 2004
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2E E Kors, K R J Vanmolkot, J Haan, et al.Cephalalgia : an International Journal of Headache|November 25, 2005
The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraineJ J Hottenga, K R J Vanmolkot, E E Kors, et al.Neurogenetics|May 11, 2004
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2M A Kaunisto, H Harno, K R J Vanmolkot, et al.Neuropediatrics|January 20, 2007
Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1B de Vries, J Haan, A H Stam, et al.Cephalalgia : an International Journal of Headache|February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsyM-J Castro, A H Stam, C Lemos, et al.Cephalalgia : an International Journal of Headache|May 24, 2008
CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhoodB de Vries, A H Stam, F Beker, et al.Journal of Neurology|November 7, 2002
Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A geneA M J M van den Maagdenberg, E E Kors, E R Brunt, et al.Neurology|January 15, 2010
Shared genetic factors in migraine and depression: evidence from a genetic isolateA H Stam, B de Vries, A C J W Janssens, et al.Clinical Genetics|November 22, 2007
Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypesM-J Castro, B Nunes, B de Vries, et al.Pageof 2