These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
227 related articles for article (PubMed ID: 19368856)
1. Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population. Corominas R; Ribasés M; Cuenca-León E; Narberhaus B; Serra SA; del Toro M; Roig M; Fernández-Fernández JM; Macaya A; Cormand B Neurosci Lett; 2009 May; 455(2):105-9. PubMed ID: 19368856 [TBL] [Abstract][Full Text] [Related]
2. Evidence of syntaxin 1A involvement in migraine susceptibility: a Portuguese study. Lemos C; Pereira-Monteiro J; Mendonça D; Ramos EM; Barros J; Sequeiros J; Alonso I; Sousa A Arch Neurol; 2010 Apr; 67(4):422-7. PubMed ID: 20385907 [TBL] [Abstract][Full Text] [Related]
3. Association analysis of STX1A gene variants in common forms of migraine. Tropeano M; Wöber-Bingöl C; Karwautz A; Wagner G; Vassos E; Campos-de-Sousa S; Graggaber A; Zesch HE; Kienbacher C; Natriashvili S; Kanbur I; Wöber C; Collier DA Cephalalgia; 2012 Feb; 32(3):203-12. PubMed ID: 22250207 [TBL] [Abstract][Full Text] [Related]
4. Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility. Curtain R; Sundholm J; Lea R; Ovcaric M; MacMillan J; Griffiths L BMC Med Genet; 2005 Sep; 6():32. PubMed ID: 16162291 [TBL] [Abstract][Full Text] [Related]
5. Influence of MTHFR genotype on contingent negative variation and MRI abnormalities in migraine. de Tommaso M; Difruscolo O; Sardaro M; Losito L; Serpino C; Pietrapertosa A; Santeramo MT; Dicuonzo F; Carella A; Lamberti P; Livrea P Headache; 2007 Feb; 47(2):253-65. PubMed ID: 17300365 [TBL] [Abstract][Full Text] [Related]
6. Association analysis of 5-HTTLPR variants, 5-HT2a receptor gene 102T/C polymorphism and migraine. Juhasz G; Zsombok T; Laszik A; Gonda X; Sotonyi P; Faludi G; Bagdy G J Neurogenet; 2003; 17(2-3):231-40. PubMed ID: 14668201 [TBL] [Abstract][Full Text] [Related]
7. A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes. Mochi M; Cevoli S; Cortelli P; Pierangeli G; Soriani S; Scapoli C; Montagna P Neurol Sci; 2003 Feb; 23(6):301-5. PubMed ID: 12624717 [TBL] [Abstract][Full Text] [Related]
8. Single nucleotide polymorphisms of the serotonin transporter gene in migraine--an association study. Bayerer B; Engelbergs J; Savidou I; Boes T; Küper M; Schorn CF; Wissmann A; Knop D; Diener HC; Limmroth V Headache; 2010 Feb; 50(2):319-22. PubMed ID: 19845785 [TBL] [Abstract][Full Text] [Related]
9. The 1246G-->A polymorphism of the HCRTR2 gene is not associated with migraine. Pinessi L; Binello E; De Martino P; Gallone S; Gentile S; Rainero I; Rivoiro C; Rubino E; Savi L; Valfrè W; Vaula G Cephalalgia; 2007 Aug; 27(8):945-9. PubMed ID: 17645762 [TBL] [Abstract][Full Text] [Related]
10. Replication study of the insulin receptor gene in migraine with aura. Netzer C; Freudenberg J; Heinze A; Heinze-Kuhn K; Goebel I; McCarthy LC; Roses AD; Göbel H; Todt U; Kubisch C Genomics; 2008 Jun; 91(6):503-7. PubMed ID: 18455362 [TBL] [Abstract][Full Text] [Related]
11. Role of the ACE ID and MTHFR C677T polymorphisms in genetic susceptibility of migraine in a north Indian population. Joshi G; Pradhan S; Mittal B J Neurol Sci; 2009 Feb; 277(1-2):133-7. PubMed ID: 19081115 [TBL] [Abstract][Full Text] [Related]
12. Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura. Fernandez F; Lea RA; Colson NJ; Bellis C; Quinlan S; Griffiths LR J Neurol Sci; 2006 Dec; 251(1-2):118-23. PubMed ID: 17095019 [TBL] [Abstract][Full Text] [Related]
13. Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine case-control cohort. Maher BH; Taylor M; Stuart S; Okolicsanyi RK; Roy B; Sutherland HG; Haupt LM; Griffiths LR Gene; 2013 Oct; 528(2):343-6. PubMed ID: 23911303 [TBL] [Abstract][Full Text] [Related]
14. Rare missense variants in ATP1A2 in families with clustering of common forms of migraine. Todt U; Dichgans M; Jurkat-Rott K; Heinze A; Zifarelli G; Koenderink JB; Goebel I; Zumbroich V; Stiller A; Ramirez A; Friedrich T; Göbel H; Kubisch C Hum Mutat; 2005 Oct; 26(4):315-21. PubMed ID: 16110494 [TBL] [Abstract][Full Text] [Related]
15. The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility. D'Onofrio M; Ambrosini A; Di Mambro A; Arisi I; Santorelli FM; Grieco GS; Nicoletti F; Nappi G; Pierelli F; Schoenen J; Buzzi MG Neurosci Lett; 2009 Mar; 453(1):12-5. PubMed ID: 19429006 [TBL] [Abstract][Full Text] [Related]
16. Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura. Todt U; Freudenberg J; Goebel I; Heinze A; Heinze-Kuhn K; Rietschel M; Göbel H; Kubisch C Neurology; 2006 Nov; 67(9):1707-9. PubMed ID: 17101915 [TBL] [Abstract][Full Text] [Related]
19. Lack of association of endothelial nitric oxide synthase polymorphisms and migraine. Toriello M; Oterino A; Pascual J; Castillo J; Colás R; Alonso-Arranz A; Ruiz-Alegría C; Quintela E; Montón F; Ruiz-Lavilla N Headache; 2008 Jul; 48(7):1115-9. PubMed ID: 18687083 [TBL] [Abstract][Full Text] [Related]
20. A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample. Sintas C; Carreño O; Fernández-Morales J; Cacheiro P; Sobrido MJ; Narberhaus B; Pozo-Rosich P; Macaya A; Cormand B Cephalalgia; 2012 Oct; 32(14):1076-80. PubMed ID: 22908361 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]