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Journal Abstract Search

483 related items for PubMed ID: 18498393

  • 1. CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.
    de Vries B, Stam AH, Beker F, van den Maagdenberg AM, Vanmolkot KR, Laan L, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD.
    Cephalalgia; 2008 Aug; 28(8):887-91. PubMed ID: 18498393
    [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
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  • 3. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
    Alonso I, Barros J, Tuna A, Coelho J, Sequeiros J, Silveira I, Coutinho P.
    Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077
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  • 4. Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1.
    de Vries B, Haan J, Stam AH, Vanmolkot KR, Stroink H, Laan LA, Gill DS, Pascual J, Frants RR, van den Maagdenberg AM, Ferrari MD.
    Neuropediatrics; 2006 Oct; 37(5):302-4. PubMed ID: 17236110
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  • 5. 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
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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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 14; 55(6):884-7. PubMed ID: 15174025
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  • 8. [From gene to disease; from CACNA1A to migraine].
    Kors EE, Haan J, Frants RR, Ferrari MD.
    Ned Tijdschr Geneeskd; 2001 Feb 10; 145(6):266-7. PubMed ID: 11236374
    [Abstract] [Full Text] [Related]

  • 9. Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene.
    Haan J, Kors EE, Terwindt GM, Vermeulen FL, Vergouwe MN, van den Maagdenberg AM, Gill DS, Pascual J, Ophoff RA, Frants RR, Ferrari.
    Cephalalgia; 2000 Oct 10; 20(8):696-700. PubMed ID: 11167897
    [Abstract] [Full Text] [Related]

  • 10. A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood.
    Weller CM, Leen WG, Neville BG, Duncan JS, de Vries B, Geilenkirchen MA, Haan J, Kamsteeg EJ, Ferrari MD, van den Maagdenberg AM, Willemsen MA, Scheffer H, Terwindt GM.
    Cephalalgia; 2015 Jan 10; 35(1):10-5. PubMed ID: 24824604
    [Abstract] [Full Text] [Related]

  • 11. 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 10; 14(5):555-60. PubMed ID: 16538223
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  • 14. Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation.
    Carreño O, García-Silva MT, García-Campos Ó, Martínez-de Aragón A, Cormand B, Macaya A.
    Headache; 2011 May 10; 51(10):1542-6. PubMed ID: 22082423
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  • 18. Genetic heterogeneity in Italian families with familial hemiplegic migraine.
    Carrera P, Piatti M, Stenirri S, Grimaldi LM, Marchioni E, Curcio M, Righetti PG, Ferrari M, Gelfi C.
    Neurology; 1999 Jul 13; 53(1):26-33. PubMed ID: 10408532
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