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.
314 related articles for article (PubMed ID: 15167062)
21. Familial basilar migraine associated with a new mutation in the ATP1A2 gene. Ambrosini A; D'Onofrio M; Grieco GS; Di Mambro A; Montagna G; Fortini D; Nicoletti F; Nappi G; Sances G; Schoenen J; Buzzi MG; Santorelli FM; Pierelli F Neurology; 2005 Dec; 65(11):1826-8. PubMed ID: 16344534 [TBL] [Abstract][Full Text] [Related]
22. Migraine genetics: an update. Haan J; Kors EE; Vanmolkot KR; van den Maagdenberg AM; Frants RR; Ferrari MD Curr Pain Headache Rep; 2005 Jun; 9(3):213-20. PubMed ID: 15907261 [TBL] [Abstract][Full Text] [Related]
23. Migraine: gene mutations and functional consequences. van den Maagdenberg AM; Haan J; Terwindt GM; Ferrari MD Curr Opin Neurol; 2007 Jun; 20(3):299-305. PubMed ID: 17495624 [TBL] [Abstract][Full Text] [Related]
24. A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2. Kaunisto MA; Harno H; Vanmolkot KR; Gargus JJ; Sun G; Hämäläinen E; Liukkonen E; Kallela M; van den Maagdenberg AM; Frants RR; Färkkilä M; Palotie A; Wessman M Neurogenetics; 2004 Jun; 5(2):141-6. PubMed ID: 15133718 [TBL] [Abstract][Full Text] [Related]
25. Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus. Jones KW; Ehm MG; Pericak-Vance MA; Haines JL; Boyd PR; Peroutka SJ Genomics; 2001 Dec; 78(3):150-4. PubMed ID: 11735221 [TBL] [Abstract][Full Text] [Related]
26. Toward a molecular genetic classification of familial hemiplegic migraine. Haan J; Kors EE; van den Maagdenberg AM; Vanmolkot KR; Terwindt GM; Frants RR; Ferrari MD Curr Pain Headache Rep; 2004 Jun; 8(3):238-43. PubMed ID: 15115644 [TBL] [Abstract][Full Text] [Related]
27. [Genetics of migraine]. Ducros A Pathol Biol (Paris); 2000 Sep; 48(7):658-62. PubMed ID: 11072644 [TBL] [Abstract][Full Text] [Related]
28. Genomewide significant linkage to migrainous headache on chromosome 5q21. Nyholt DR; Morley KI; Ferreira MA; Medland SE; Boomsma DI; Heath AC; Merikangas KR; Montgomery GW; Martin NG Am J Hum Genet; 2005 Sep; 77(3):500-12. PubMed ID: 16080125 [TBL] [Abstract][Full Text] [Related]
30. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. Vanmolkot KR; Kors EE; Turk U; Turkdogan D; Keyser A; Broos LA; Kia SK; van den Heuvel JJ; Black DF; Haan J; Frants RR; Barone V; Ferrari MD; Casari G; Koenderink JB; van den Maagdenberg AM Eur J Hum Genet; 2006 May; 14(5):555-60. PubMed ID: 16538223 [TBL] [Abstract][Full Text] [Related]
31. [Genetics of migraine]. Ducros A Rev Neurol (Paris); 2013 May; 169(5):360-71. PubMed ID: 23618705 [TBL] [Abstract][Full Text] [Related]
32. Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family. Cevoli S; Pierangeli G; Monari L; Valentino ML; Bernardoni P; Mochi M; Cortelli P; Montagna P Neurol Sci; 2002 Apr; 23(1):7-10. PubMed ID: 12111614 [TBL] [Abstract][Full Text] [Related]
33. FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2. Wiwanitkit V J Neurol Sci; 2009 Feb; 277(1-2):76-9. PubMed ID: 19007941 [TBL] [Abstract][Full Text] [Related]
34. A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation. De Cunto A; Bensa M; Tonelli A Pediatr Neurol; 2012 Aug; 47(2):133-6. PubMed ID: 22759692 [TBL] [Abstract][Full Text] [Related]
36. Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene. Roth C; Freilinger T; Kirovski G; Dunkel J; Shah Y; Wilken B; Rautenstrauß B; Ferbert A Cephalalgia; 2014 Mar; 34(3):183-90. PubMed ID: 24096472 [TBL] [Abstract][Full Text] [Related]
37. Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches. Alfayyadh MM; Maksemous N; Sutherland HG; Lea RA; Griffiths LR Genes (Basel); 2024 Mar; 15(4):. PubMed ID: 38674378 [TBL] [Abstract][Full Text] [Related]
38. Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility. Lea RA; Curtain RP; Hutchins C; Brimage PJ; Griffiths LR Am J Med Genet; 2001 Dec; 105(8):707-12. PubMed ID: 11803518 [TBL] [Abstract][Full Text] [Related]
39. Significant linkage to migraine with aura on chromosome 11q24. Cader ZM; Noble-Topham S; Dyment DA; Cherny SS; Brown JD; Rice GP; Ebers GC Hum Mol Genet; 2003 Oct; 12(19):2511-7. PubMed ID: 12915447 [TBL] [Abstract][Full Text] [Related]
40. Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine. Tonelli A; Gallanti A; Bersano A; Cardin V; Ballabio E; Airoldi G; Redaelli F; Candelise L; Bresolin N; Bassi MT Clin Genet; 2007 Dec; 72(6):517-23. PubMed ID: 17877748 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]