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)

  • 21. Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.
    Huang H; Millat G; Rodriguez-Lafrasse C; Rousson R; Kugener B; Chevalier P; Chahine M
    FEBS Lett; 2009 Mar; 583(5):890-6. PubMed ID: 19302788
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Inherited and acquired vulnerability to ventricular arrhythmias: cardiac Na+ and K+ channels.
    Clancy CE; Kass RS
    Physiol Rev; 2005 Jan; 85(1):33-47. PubMed ID: 15618477
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.
    Diamant UB; Vahedi F; Winbo A; Rydberg A; Stattin EL; Jensen SM; Bergfeldt L
    J Appl Physiol (1985); 2013 Nov; 115(10):1423-32. PubMed ID: 24052033
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular basis of the long-QT syndrome associated with deafness.
    Splawski I; Timothy KW; Vincent GM; Atkinson DL; Keating MT
    N Engl J Med; 1997 May; 336(22):1562-7. PubMed ID: 9164812
    [No Abstract]   [Full Text] [Related]  

  • 25. Third and long (QT).
    Nat Genet; 1996 Jan; 12(1):1-2. PubMed ID: 8528237
    [No Abstract]   [Full Text] [Related]  

  • 26. Flecainide, a therapeutic option in a patient with long QT syndrome type 3 caused by the heterozygous V411M mutation in the SCN5A gene.
    Carrasco JI; Izquierdo I; Medina P; Arnau MÁ; Salvador A; Zorio E
    Rev Esp Cardiol (Engl Ed); 2012 Nov; 65(11):1058-9. PubMed ID: 22721569
    [No Abstract]   [Full Text] [Related]  

  • 27. Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy.
    van Hoeijen DA; Blom MT; Tan HL
    Expert Opin Pharmacother; 2014 Sep; 15(13):1875-87. PubMed ID: 24992280
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Ionic channel pathies].
    Yang T; Yao WX; Jiang MX
    Sheng Li Ke Xue Jin Zhan; 1998 Jul; 29(3):239-42. PubMed ID: 12501643
    [No Abstract]   [Full Text] [Related]  

  • 29. Genetic risk for acquired arrhythmia.
    Behr ER; McKenna WJ
    Trends Genet; 2003 Sep; 19(9):470-3. PubMed ID: 12957537
    [No Abstract]   [Full Text] [Related]  

  • 30. George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.
    Splawski I; Timothy KW; Vincent GM; Atkinson DL; Keating MT
    Proc Assoc Am Physicians; 1997 Sep; 109(5):504-11. PubMed ID: 9285950
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Cardiac ion channel disorders--diagnosis and treatment].
    Haugaa KH; Berge KE; Früh A; Anfinsen OG; Arnestad M; Hallerud M; Gjesdal K; Leren TP; Amlie JP
    Tidsskr Nor Laegeforen; 2005 Oct; 125(20):2778-81. PubMed ID: 16244679
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Is it time to develop a "pathogenicity" score to distinguish long QT syndrome causing mutations from "background" genetic noise?
    Darbar D
    Heart Rhythm; 2009 Sep; 6(9):1304-5. PubMed ID: 19716086
    [No Abstract]   [Full Text] [Related]  

  • 33. Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds.
    Skinner JR; Crawford J; Smith W; Aitken A; Heaven D; Evans CA; Hayes I; Neas KR; Stables S; Koelmeyer T; Denmark L; Vuletic J; Maxwell F; White K; Yang T; Roden DM; Leren TP; Shelling A; Love DR;
    Heart Rhythm; 2011 Mar; 8(3):412-9. PubMed ID: 21070882
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.
    Paulussen A; Matthijs G; Gewillig M; Verhasselt P; Cohen N; Aerssens J
    Genet Test; 2003; 7(1):57-61. PubMed ID: 12820704
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
    Allan WC; Timothy K; Vincent GM; Palomaki GE; Neveux LM; Haddow JE
    J Med Screen; 2001; 8(4):173-7. PubMed ID: 11743032
    [TBL] [Abstract][Full Text] [Related]  

  • 36. More on the history of arrhythmia in long QT syndrome.
    Csanády M
    J Am Coll Cardiol; 2004 Sep; 44(6):1339; author reply 1339. PubMed ID: 15364343
    [No Abstract]   [Full Text] [Related]  

  • 37. Sodium-channel blockers might contribute to the prevention of ventricular tachycardia in patients with long QT syndrome type 2: a description of 4 cases.
    Ildarova R; Shkolnikova MA; Kharlap M; Bereznitskaya V; Kalinin L
    J Electrocardiol; 2012; 45(3):237-43. PubMed ID: 22402334
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cardiac sodium channel dysfunction in sudden infant death syndrome.
    Wang DW; Desai RR; Crotti L; Arnestad M; Insolia R; Pedrazzini M; Ferrandi C; Vege A; Rognum T; Schwartz PJ; George AL
    Circulation; 2007 Jan; 115(3):368-76. PubMed ID: 17210841
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic disorders of ion channels.
    Enkvetchakul D
    Mo Med; 2010; 107(4):270-5. PubMed ID: 20806840
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Congenital long QT syndrome and 2:1 atrioventricular block with a mutation of the SCN5A gene.
    Miura M; Yamagishi H; Morikawa Y; Matsuoka R
    Pediatr Cardiol; 2003; 24(1):70-2. PubMed ID: 12574983
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.