BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 12808265)

  • 1. Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
    Inoue M; Shimizu M; Ino H; Yamaguchi M; Terai H; Hayashi K; Kiyama M; Sakata K; Hayashi T; Mabuchi H
    Circ J; 2003 Jun; 67(6):495-8. PubMed ID: 12808265
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
    Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
    J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.
    Lupoglazoff JM; Denjoy I; Berthet M; Neyroud N; Demay L; Richard P; Hainque B; Vaksmann G; Klug D; Leenhardt A; Maillard G; Coumel P; Guicheney P
    Circulation; 2001 Feb; 103(8):1095-101. PubMed ID: 11222472
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
    Zareba W; Moss AJ; Locati EH; Lehmann MH; Peterson DR; Hall WJ; Schwartz PJ; Vincent GM; Priori SG; Benhorin J; Towbin JA; Robinson JL; Andrews ML; Napolitano C; Timothy K; Zhang L; Medina A;
    J Am Coll Cardiol; 2003 Jul; 42(1):103-9. PubMed ID: 12849668
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].
    Lupoglazoff JM; Denjoy I; Berthet M; Hainque B; Vaksmann G; Klug D; Villain E; Lucet V; Guicheney P; Coumel P
    Arch Mal Coeur Vaiss; 2001 May; 94(5):470-8. PubMed ID: 11434015
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multi-undulant T-U-wave, sinus bradycardia and long QT syndrome: a possible phenotype of mutant genes controlling the inward potassium rectifiers.
    Shen CT; Wu YC; Yu SS; Wang NK
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(4):267-75. PubMed ID: 9297927
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
    Jongbloed RJ; Wilde AA; Geelen JL; Doevendans P; Schaap C; Van Langen I; van Tintelen JP; Cobben JM; Beaufort-Krol GC; Geraedts JP; Smeets HJ
    Hum Mutat; 1999; 13(4):301-10. PubMed ID: 10220144
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates.
    Chevalier P; Rodriguez C; Bontemps L; Miquel M; Kirkorian G; Rousson R; Potet F; Schott JJ; BarĂ³ I; Touboul P
    Cardiovasc Res; 2001 May; 50(2):386-98. PubMed ID: 11334843
    [TBL] [Abstract][Full Text] [Related]  

  • 9. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
    Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
    Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The long QT syndromes: genetic basis and clinical implications.
    Chiang CE; Roden DM
    J Am Coll Cardiol; 2000 Jul; 36(1):1-12. PubMed ID: 10898405
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital and acquired long QT syndrome.
    Camm AJ; Janse MJ; Roden DM; Rosen MR; Cinca J; Cobbe SM
    Eur Heart J; 2000 Aug; 21(15):1232-7. PubMed ID: 10924312
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.
    Benhorin J; Moss AJ; Bak M; Zareba W; Kaufman ES; Kerem B; Towbin JA; Priori S; Kass RS; Attali B; Brown AM; Ficker E
    Ann Noninvasive Electrocardiol; 2002 Jan; 7(1):40-6. PubMed ID: 11844290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome.
    Moennig G; Schulze-Bahr E; Wedekind H; Borggrefe M; Funke H; Toelle M; Kirchhof P; Eckardt L; Assmann G; Breithardt G; Haverkamp W
    Pacing Clin Electrophysiol; 2001 Apr; 24(4 Pt 1):406-15. PubMed ID: 11341076
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
    Berthet M; Denjoy I; Donger C; Demay L; Hammoude H; Klug D; Schulze-Bahr E; Richard P; Funke H; Schwartz K; Coumel P; Hainque B; Guicheney P
    Circulation; 1999 Mar; 99(11):1464-70. PubMed ID: 10086971
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations.
    Etheridge SP; Compton SJ; Tristani-Firouzi M; Mason JW
    J Am Coll Cardiol; 2003 Nov; 42(10):1777-82. PubMed ID: 14642687
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C
    J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.