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Journal Abstract Search

159 related items for PubMed ID: 9043864

  • 1. A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.
    Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Mohrenweiser H, Litt M, Hofker MH, Haan J, Ferrari MD, Frants RR.
    Eur J Hum Genet; 1996; 4(6):321-8. PubMed ID: 9043864
    [Abstract] [Full Text] [Related]

  • 2. Familial hemiplegic migraine: involvement of a calcium neuronal channel.
    Ophoff RA, Terwindt GM, Vergouwe MN, Frants RR, Ferrari MD.
    Neurologia; 1997 Dec; 12 Suppl 5():31-7. PubMed ID: 9436352
    [Abstract] [Full Text] [Related]

  • 3. Genetic heterogeneity of familial hemiplegic migraine.
    Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR.
    Genomics; 1994 Jul 01; 22(1):21-6. PubMed ID: 7959770
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  • 4. [Familial hemiplegic migraine].
    Thomsen LL, Olesen J, Russell MB.
    Ugeskr Laeger; 1998 Sep 07; 160(37):5325-9. PubMed ID: 9748855
    [Abstract] [Full Text] [Related]

  • 5. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.
    Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, Verier A, Echenne B, Lopez de Munain A, Bousser MG, Tournier-Lasserve E.
    Ann Neurol; 1997 Dec 07; 42(6):885-90. PubMed ID: 9403481
    [Abstract] [Full Text] [Related]

  • 6. [Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].
    Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J.
    Rev Neurol (Paris); 1994 Dec 07; 150(5):340-5. PubMed ID: 7878319
    [Abstract] [Full Text] [Related]

  • 7. 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 07; 130(Pt 2):346-56. PubMed ID: 17142831
    [Abstract] [Full Text] [Related]

  • 8. 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 07; 78(3):150-4. PubMed ID: 11735221
    [Abstract] [Full Text] [Related]

  • 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 07; 14(5):555-60. PubMed ID: 16538223
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Familial migraine: exclusion of the susceptibility gene from the reported locus of familial hemiplegic migraine on 19p.
    Hovatta I, Kallela M, Färkkilä M, Peltonen L.
    Genomics; 1994 Oct 13; 23(3):707-9. PubMed ID: 7851903
    [Abstract] [Full Text] [Related]

  • 12. Familial hemiplegic migraine, nystagmus, and cerebellar atrophy.
    Elliott MA, Peroutka SJ, Welch S, May EF.
    Ann Neurol; 1996 Jan 13; 39(1):100-6. PubMed ID: 8572654
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  • 14. 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 13; 60(4):610-4. PubMed ID: 12707077
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  • 17. [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]

  • 18. No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree.
    Curtain R, Tajouri L, Lea R, MacMillan J, Griffiths L.
    Eur J Med Genet; 2006 Feb 10; 49(1):57-62. PubMed ID: 16473310
    [Abstract] [Full Text] [Related]

  • 19. Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease.
    Drenth JP, Tahvanainen E, te Morsche RH, Tahvanainen P, Kääriäinen H, Höckerstedt K, van de Kamp JM, Breuning MH, Jansen JB.
    Hepatology; 2004 Apr 10; 39(4):924-31. PubMed ID: 15057895
    [Abstract] [Full Text] [Related]

  • 20. Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.
    Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, van Eijk R, Frants RR, Ferrari MD.
    Neurology; 1998 Apr 10; 50(4):1105-10. PubMed ID: 9566402
    [Abstract] [Full Text] [Related]

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