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Journal Abstract Search

594 related items for PubMed ID: 18808722

  • 41. Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations.
    Hayashi K, Fujino N, Uchiyama K, Ino H, Sakata K, Konno T, Masuta E, Funada A, Sakamoto Y, Tsubokawa T, Nakashima K, Liu L, Higashida H, Hiramaru Y, Shimizu M, Yamagishi M.
    Clin Sci (Lond); 2009 Sep 21; 117(12):415-24. PubMed ID: 19371231
    [Abstract] [Full Text] [Related]

  • 42. Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant.
    Crotti L, Hu D, Barajas-Martinez H, De Ferrari GM, Oliva A, Insolia R, Pollevick GD, Dagradi F, Guerchicoff A, Greco F, Schwartz PJ, Viskin S, Antzelevitch C.
    Heart Rhythm; 2012 Jul 21; 9(7):1104-12. PubMed ID: 22338672
    [Abstract] [Full Text] [Related]

  • 43. A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.
    Nof E, Cordeiro JM, Pérez GJ, Scornik FS, Calloe K, Love B, Burashnikov E, Caceres G, Gunsburg M, Antzelevitch C.
    Circ Cardiovasc Genet; 2010 Apr 21; 3(2):199-206. PubMed ID: 20181576
    [Abstract] [Full Text] [Related]

  • 44. [A novel mutation of the KCNH2 gene in a family with congenital long QT syndrome].
    Lian J, Zhou J, Huang X, Wang Y, Yang X, Li D.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb 21; 27(1):77-80. PubMed ID: 20140874
    [Abstract] [Full Text] [Related]

  • 45. Identification novel LQT syndrome-associated variants in Polish population and genotype-phenotype correlations in eight families.
    Szperl M, Kozicka U, Kosiec A, Kukla P, Roszczynko M, Biernacka EK.
    J Appl Genet; 2018 Nov 21; 59(4):463-469. PubMed ID: 30244407
    [Abstract] [Full Text] [Related]

  • 46. Genetics of long QT syndrome.
    Tester DJ, Ackerman MJ.
    Methodist Debakey Cardiovasc J; 2014 Nov 21; 10(1):29-33. PubMed ID: 24932360
    [Abstract] [Full Text] [Related]

  • 47. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
    Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ.
    Heart Rhythm; 2009 Sep 21; 6(9):1297-303. PubMed ID: 19716085
    [Abstract] [Full Text] [Related]

  • 48. Mutation screening in KCNQ1, HERG, KCNE1, KCNE2 and SCN5A genes in a long QT syndrome family.
    Koo SH, Teo WS, Ching CK, Chan SH, Lee EJ.
    Ann Acad Med Singap; 2007 Jun 21; 36(6):394-8. PubMed ID: 17597962
    [Abstract] [Full Text] [Related]

  • 49. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.
    Koopmann TT, Alders M, Jongbloed RJ, Guerrero S, Mannens MM, Wilde AA, Bezzina CR.
    Heart Rhythm; 2006 Jan 21; 3(1):52-5. PubMed ID: 16399053
    [Abstract] [Full Text] [Related]

  • 50. Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation.
    Barsheshet A, Moss AJ, McNitt S, Polonsky S, Lopes CM, Zareba W, Robinson JL, Ackerman MJ, Benhorin J, Kaufman ES, Towbin JA, Vincent GM, Qi M, Goldenberg I.
    Circ Cardiovasc Genet; 2011 Oct 21; 4(5):491-9. PubMed ID: 21831960
    [Abstract] [Full Text] [Related]

  • 51. Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes.
    Lehtonen A, Fodstad H, Laitinen-Forsblom P, Toivonen L, Kontula K, Swan H.
    Heart Rhythm; 2007 May 21; 4(5):603-7. PubMed ID: 17467628
    [Abstract] [Full Text] [Related]

  • 52. High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance.
    Steffensen AB, Refaat MM, David JP, Mujezinovic A, Calloe K, Wojciak J, Nussbaum RL, Scheinman MM, Schmitt N.
    Sci Rep; 2015 Jun 12; 5():10009. PubMed ID: 26066609
    [Abstract] [Full Text] [Related]

  • 53. Functional significance of KCNH2 (HERG) K897T polymorphism for cardiac repolarization assessed by analysis of T-wave morphology.
    Linna EH, Perkiömäki JS, Karsikas M, Seppänen T, Savolainen M, Kesäniemi YA, Mäkikallio T, Huikuri HV.
    Ann Noninvasive Electrocardiol; 2006 Jan 12; 11(1):57-62. PubMed ID: 16472284
    [Abstract] [Full Text] [Related]

  • 54. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
    Paulussen AD, Gilissen RA, Armstrong M, Doevendans PA, Verhasselt P, Smeets HJ, Schulze-Bahr E, Haverkamp W, Breithardt G, Cohen N, Aerssens J.
    J Mol Med (Berl); 2004 Mar 12; 82(3):182-8. PubMed ID: 14760488
    [Abstract] [Full Text] [Related]

  • 55. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
    Tester DJ, Will ML, Haglund CM, Ackerman MJ.
    Heart Rhythm; 2005 May 12; 2(5):507-17. PubMed ID: 15840476
    [Abstract] [Full Text] [Related]

  • 56. Clinical presentation and genetic characterization of early-onset atrial fibrillation in patients affected by long QT syndrome: A single-center experience.
    Sarubbi B, Ciriello GD, Barretta F, Sorice D, Orlando A, Correra A, Colonna D, Uomo F, Mazzaccara C, D'Argenio V, Romeo E, Frisso G.
    J Cardiovasc Electrophysiol; 2024 Oct 12; 35(10):1941-1951. PubMed ID: 39082327
    [Abstract] [Full Text] [Related]

  • 57. Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.
    Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW.
    Circ Arrhythm Electrophysiol; 2013 Oct 12; 6(5):946-51. PubMed ID: 23995044
    [Abstract] [Full Text] [Related]

  • 58. Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients.
    Li L, Shen C, Yao Z, Liang J, Huang C.
    Genet Test Mol Biomarkers; 2015 Jul 12; 19(7):359-65. PubMed ID: 26066992
    [Abstract] [Full Text] [Related]

  • 59. The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmia.
    Scherer CR, Lerche C, Decher N, Dennis AT, Maier P, Ficker E, Busch AE, Wollnik B, Steinmeyer K.
    Br J Pharmacol; 2002 Nov 12; 137(6):892-900. PubMed ID: 12411421
    [Abstract] [Full Text] [Related]

  • 60. N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome.
    Ohno S, Zankov DP, Yoshida H, Tsuji K, Makiyama T, Itoh H, Akao M, Hancox JC, Kita T, Horie M.
    Heart Rhythm; 2007 Mar 12; 4(3):332-40. PubMed ID: 17341399
    [Abstract] [Full Text] [Related]

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