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The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
Vanmolkot KR, Babini E, de Vries B, Stam AH, Freilinger T, Terwindt GM, Norris L, Haan J, Frants RR, Ramadan NM, Ferrari MD, Pusch M, van den Maagdenberg AM, Dichgans M. Vanmolkot KR, et al. Among authors: dichgans m. Hum Mutat. 2007 May;28(5):522. doi: 10.1002/humu.9486. Hum Mutat. 2007. PMID: 17397047
Divergent sodium channel defects in familial hemiplegic migraine.
Kahlig KM, Rhodes TH, Pusch M, Freilinger T, Pereira-Monteiro JM, Ferrari MD, van den Maagdenberg AM, Dichgans M, George AL Jr. Kahlig KM, et al. Among authors: dichgans m. Proc Natl Acad Sci U S A. 2008 Jul 15;105(28):9799-804. doi: 10.1073/pnas.0711717105. Epub 2008 Jul 9. Proc Natl Acad Sci U S A. 2008. PMID: 18621678 Free PMC article.
A high-density association screen of 155 ion transport genes for involvement with common migraine.
Nyholt DR, LaForge KS, Kallela M, Alakurtti K, Anttila V, Färkkilä M, Hämaläinen E, Kaprio J, Kaunisto MA, Heath AC, Montgomery GW, Göbel H, Todt U, Ferrari MD, Launer LJ, Frants RR, Terwindt GM, de Vries B, Verschuren WM, Brand J, Freilinger T, Pfaffenrath V, Straube A, Ballinger DG, Zhan Y, Daly MJ, Cox DR, Dichgans M, van den Maagdenberg AM, Kubisch C, Martin NG, Wessman M, Peltonen L, Palotie A. Nyholt DR, et al. Among authors: dichgans m. Hum Mol Genet. 2008 Nov 1;17(21):3318-31. doi: 10.1093/hmg/ddn227. Epub 2008 Aug 2. Hum Mol Genet. 2008. PMID: 18676988 Free PMC article.
683 results