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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

428 related items for PubMed ID: 17877748

  • 1. 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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  • 2. The genetic spectrum of a population-based sample of familial hemiplegic migraine.
    Thomsen LL, Kirchmann M, Bjornsson A, Stefansson H, Jensen RM, Fasquel AC, Petursson H, Stefansson M, Frigge ML, Kong A, Gulcher J, Stefansson K, Olesen J.
    Brain; 2007 Feb; 130(Pt 2):346-56. PubMed ID: 17142831
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  • 4. 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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  • 7. ATP1A2 mutations in 11 families with familial hemiplegic migraine.
    Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J, Bousser MG, Casari G, Tournier-Lasserve E.
    Hum Mutat; 2005 Sep; 26(3):281. PubMed ID: 16088919
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  • 8. A novel ATP1A2 mutation in a family with FHM type II.
    Pierelli F, Grieco GS, Pauri F, Pirro C, Fiermonte G, Ambrosini A, Costa A, Buzzi MG, Valoppi M, Caltagirone C, Nappi G, Santorelli FM.
    Cephalalgia; 2006 Mar; 26(3):324-8. PubMed ID: 16472340
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  • 9. 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
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  • 10. Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
    Vahedi K, Depienne C, Le Fort D, Riant F, Chaine P, Trouillard O, Gaudric A, Morris MA, Leguern E, Tournier-Lasserve E, Bousser MG.
    Neurology; 2009 Mar 31; 72(13):1178-83. PubMed ID: 19332696
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  • 13. De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
    Riant F, Ducros A, Ploton C, Barbance C, Depienne C, Tournier-Lasserve E.
    Neurology; 2010 Sep 14; 75(11):967-72. PubMed ID: 20837964
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  • 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 14; 26(4):315-21. PubMed ID: 16110494
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  • 20. Two novel SCN1A mutations identified in families with familial hemiplegic migraine.
    Weller CM, Pelzer N, de Vries B, López MA, De Fàbregues O, Pascual J, Arroyo MA, Koelewijn SC, Stam AH, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM.
    Cephalalgia; 2014 Nov 14; 34(13):1062-9. PubMed ID: 24707016
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