These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 9820986)

  • 1. Molecular genetics of inherited long QT syndromes.
    Geelen JL; Doevendans PA; Jongbloed RJ; Wellens HJ; Geraedts JP
    Eur Heart J; 1998 Oct; 19(10):1427-33. PubMed ID: 9820986
    [No Abstract]   [Full Text] [Related]  

  • 2. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM
    Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM; Timothy K; Fox J; Zhang L
    Cardiol Rev; 1999; 7(1):44-55. PubMed ID: 10348966
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.
    Surber R; Hensellek S; Prochnau D; Werner GS; Benndorf K; Figulla HR; Zimmer T
    Cardiovasc Res; 2008 Mar; 77(4):740-8. PubMed ID: 18065446
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital long-QT syndromes: a clinical and genetic update from infancy through adulthood.
    Webster G; Berul CI
    Trends Cardiovasc Med; 2008 Aug; 18(6):216-24. PubMed ID: 19185812
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Long QT syndrome].
    Nakajima T; Kaneko Y; Taniguchi Y; Nagai R
    Nihon Rinsho; 1996 Mar; 54(3):776-81. PubMed ID: 8904236
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular cardiology. Ion channels lose the rhythm.
    Welsh MJ; Hoshi T
    Nature; 1995 Aug; 376(6542):640. PubMed ID: 7651510
    [No Abstract]   [Full Text] [Related]  

  • 8. Long QT syndrome: from channels to cardiac arrhythmias.
    Moss AJ; Kass RS
    J Clin Invest; 2005 Aug; 115(8):2018-24. PubMed ID: 16075042
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [DNA-based diagnostics of long QT syndrome].
    Berge KE; Haugaa KH; Anfinsen OG; Früh A; Hallerud M; Jonsrud C; Øyen N; Gjesdal K; Amlie JP; Leren TP
    Tidsskr Nor Laegeforen; 2005 Oct; 125(20):2783-6. PubMed ID: 16244680
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation.
    Benito B; Brugada R; Perich RM; Lizotte E; Cinca J; Mont L; Berruezo A; Tolosana JM; Freixa X; Brugada P; Brugada J
    Heart Rhythm; 2008 Oct; 5(10):1434-40. PubMed ID: 18929331
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death].
    Fosdal I; Wettrell G; Christiansen M; Kanters JK; Larsen LA
    Lakartidningen; 2001 Feb; 98(8):810-5. PubMed ID: 11265565
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biology.
    Priori SG; Cantù F; Schwartz PJ
    Schweiz Med Wochenschr; 1996 Oct; 126(41):1727-31. PubMed ID: 8893413
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Congenital long QT syndromes].
    Le Marec H; Schott JJ
    Arch Mal Coeur Vaiss; 1997 Jun; 90 Spec No 3():25-35. PubMed ID: 9295920
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A molecular basis for the therapy of the long QT syndrome.
    Priori SG; Napolitano C; Schwartz PJ
    Arch Mal Coeur Vaiss; 1996 Sep; 89(9):1185-7. PubMed ID: 8952843
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular screening of long-QT syndrome: risk is there, or rare?
    Aiba T; Shimizu W
    Heart Rhythm; 2011 Mar; 8(3):420-1. PubMed ID: 21130900
    [No Abstract]   [Full Text] [Related]  

  • 16. Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions.
    Syrris P; Murray A; Carter ND; McKenna WM; Jeffery S
    J Med Genet; 2001 Oct; 38(10):705-10. PubMed ID: 11594341
    [No Abstract]   [Full Text] [Related]  

  • 17. Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
    Arnestad M; Crotti L; Rognum TO; Insolia R; Pedrazzini M; Ferrandi C; Vege A; Wang DW; Rhodes TE; George AL; Schwartz PJ
    Circulation; 2007 Jan; 115(3):361-7. PubMed ID: 17210839
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.
    Van Langen IM; Birnie E; Alders M; Jongbloed RJ; Le Marec H; Wilde AA
    J Med Genet; 2003 Feb; 40(2):141-5. PubMed ID: 12566525
    [No Abstract]   [Full Text] [Related]  

  • 19. On optimizing therapies, Orai, and ORNs.
    Adler EM
    J Gen Physiol; 2013 Feb; 141(2):149-50. PubMed ID: 23359279
    [No Abstract]   [Full Text] [Related]  

  • 20. Molecular basis of ranolazine block of LQT-3 mutant sodium channels: evidence for site of action.
    Fredj S; Sampson KJ; Liu H; Kass RS
    Br J Pharmacol; 2006 May; 148(1):16-24. PubMed ID: 16520744
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.