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Journal Abstract Search

500 related items for PubMed ID: 12953268

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 3. First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
    Vanmolkot KR, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJ, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM.
    Eur J Hum Genet; 2007 Aug; 15(8):884-8. PubMed ID: 17473835
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2.
    Kors EE, Vanmolkot KR, Haan J, Kheradmand Kia S, Stroink H, Laan LA, Gill DS, Pascual J, van den Maagdenberg AM, Frants RR, Ferrari MD.
    Neuropediatrics; 2004 Oct; 35(5):293-6. PubMed ID: 15534763
    [Abstract] [Full Text] [Related]

  • 10. Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian family.
    Spacey SD, Vanmolkot KR, Murphy C, van den Maagdenberg AM, Hsiung RG.
    Headache; 2005 Oct; 45(9):1244-9. PubMed ID: 16178956
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. 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 13; 65(11):1826-8. PubMed ID: 16344534
    [Abstract] [Full Text] [Related]

  • 13. No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures.
    Martinelli Boneschi F, Aridon P, Zara F, Guerrini R, Marini C, De Fusco M, Comi G, Casari G.
    Neurosci Lett; 2005 Nov 11; 388(2):71-4. PubMed ID: 16026932
    [Abstract] [Full Text] [Related]

  • 14. A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
    Gallanti A, Tonelli A, Cardin V, Bussone G, Bresolin N, Bassi MT.
    J Neurol Sci; 2008 Oct 15; 273(1-2):123-6. PubMed ID: 18644608
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 29(3):308-13. PubMed ID: 19220312
    [Abstract] [Full Text] [Related]

  • 16. Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
    Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S.
    Ann Neurol; 2004 Jun 15; 55(6):884-7. PubMed ID: 15174025
    [Abstract] [Full Text] [Related]

  • 17. Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.
    Castro MJ, Nunes B, de Vries B, Lemos C, Vanmolkot KR, van den Heuvel JJ, Temudo T, Barros J, Sequeiros J, Frants RR, Koenderink JB, Pereira-Monteiro JM, van den Maagdenberg AM.
    Clin Genet; 2008 Jan 15; 73(1):37-43. PubMed ID: 18028456
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 28(7):774-7. PubMed ID: 18498390
    [Abstract] [Full Text] [Related]

  • 19. [From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].
    Kors EE, Vanmolkot KR, Haan J, van den Maagdenberg AM, Frants RR, Ferrari MD.
    Ned Tijdschr Geneeskd; 2004 Sep 25; 148(39):1919-20. PubMed ID: 15495990
    [Abstract] [Full Text] [Related]

  • 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 25; 34(13):1062-9. PubMed ID: 24707016
    [Abstract] [Full Text] [Related]

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