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Journal Abstract Search

471 related items for PubMed ID: 19220312

  • 1. First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
    Castro MJ, Stam AH, Lemos C, de Vries B, Vanmolkot KR, Barros J, Terwindt GM, Frants RR, Sequeiros J, Ferrari MD, Pereira-Monteiro JM, van den Maagdenberg AM.
    Cephalalgia; 2009 Mar; 29(3):308-13. PubMed ID: 19220312
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  • 4. 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
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  • 5. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
    Vanmolkot KR, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WA, Black DF, Sandkuijl LA, Frants RR, Ferrari MD, van den Maagdenberg AM.
    Ann Neurol; 2003 Sep; 54(3):360-6. PubMed ID: 12953268
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  • 9. Sporadic hemiplegic migraine and epilepsy associated with CACNA1A gene mutation.
    Zangaladze A, Asadi-Pooya AA, Ashkenazi A, Sperling MR.
    Epilepsy Behav; 2010 Feb; 17(2):293-5. PubMed ID: 20071244
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  • 12. A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
    Fernandez DM, Hand CK, Sweeney BJ, Parfrey NA.
    Headache; 2008 Jan; 48(1):101-8. PubMed ID: 18184292
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  • 13. Genetics of migraine: an update with special attention to genetic comorbidity.
    Stam AH, van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD.
    Curr Opin Neurol; 2008 Jun; 21(3):288-93. PubMed ID: 18451712
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  • 15. Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene.
    Suls A, Velizarova R, Yordanova I, Deprez L, Van Dyck T, Wauters J, Guergueltcheva V, Claes LR, Kremensky I, Jordanova A, De Jonghe P.
    Neurology; 2010 Jul 06; 75(1):72-6. PubMed ID: 20484682
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  • 17. Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation.
    Lebas A, Guyant-Maréchal L, Hannequin D, Riant F, Tournier-Lasserve E, Parain D.
    Cephalalgia; 2008 Jul 06; 28(7):774-7. PubMed ID: 18498390
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