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 *

190 related articles for article (PubMed ID: 10386270)

  • 1. The genetic basis for cardiac dysrhythmias and the long QT syndrome.
    Vizgirda VM
    J Cardiovasc Nurs; 1999 Jul; 13(4):34-45. PubMed ID: 10386270
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk.
    ter Bekke RM; Haugaa KH; van den Wijngaard A; Bos JM; Ackerman MJ; Edvardsen T; Volders PG
    Eur Heart J; 2015 Jan; 36(3):179-86. PubMed ID: 25205533
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnosis, management and therapeutic strategies for congenital long QT syndrome.
    Wilde AAM; Amin AS; Postema PG
    Heart; 2022 Mar; 108(5):332-338. PubMed ID: 34039680
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Molecular genetics in the hereditary form of long QT syndrome].
    Georgijević Milić L
    Med Pregl; 2000; 53(1-2):51-4. PubMed ID: 10953551
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.
    Abriel H; Cabo C; Wehrens XH; Rivolta I; Motoike HK; Memmi M; Napolitano C; Priori SG; Kass RS
    Circ Res; 2001 Apr; 88(7):740-5. PubMed ID: 11304498
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias.
    Napolitano C; Schwartz PJ; Brown AM; Ronchetti E; Bianchi L; Pinnavaia A; Acquaro G; Priori SG
    J Cardiovasc Electrophysiol; 2000 Jun; 11(6):691-6. PubMed ID: 10868744
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Disorders of cardiac repolarization: long QT and short QT syndromes.
    Horie M; Itoh H
    Circ J; 2007; 71 Suppl A():A50-3. PubMed ID: 17587740
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ion channels, the QT interval, and arrhythmias.
    Wilde AA; Veldkamp MW
    Pacing Clin Electrophysiol; 1997 Aug; 20(8 Pt 2):2048-51. PubMed ID: 9272506
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome.
    Antzelevitch C; Yan GX; Shimizu W
    J Electrocardiol; 1999; 32 Suppl():158-65. PubMed ID: 10688320
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The genetic basis of long QT and short QT syndromes: a mutation update.
    Hedley PL; Jørgensen P; Schlamowitz S; Wangari R; Moolman-Smook J; Brink PA; Kanters JK; Corfield VA; Christiansen M
    Hum Mutat; 2009 Nov; 30(11):1486-511. PubMed ID: 19862833
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis.
    Roden DM; Spooner PM
    J Cardiovasc Electrophysiol; 1999 Dec; 10(12):1664-83. PubMed ID: 10636197
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Clinical impact of genetic studies in lethal inherited cardiac arrhythmias.
    Shimizu W
    Circ J; 2008 Dec; 72(12):1926-36. PubMed ID: 18981593
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
    Moss AJ; Zareba W; Benhorin J; Locati EH; Hall WJ; Robinson JL; Schwartz PJ; Towbin JA; Vincent GM; Lehmann MH
    Circulation; 1995 Nov; 92(10):2929-34. PubMed ID: 7586261
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Long QT syndrome: from clinical discovery to molecular etiopathogenesis].
    Czajkowski V; Kulbertus H
    Rev Med Liege; 1998 Apr; 53(4):199-207. PubMed ID: 9641014
    [TBL] [Abstract][Full Text] [Related]  

  • 17. KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
    Chen S; Zhang L; Bryant RM; Vincent GM; Flippin M; Lee JC; Brown E; Zimmerman F; Rozich R; Szafranski P; Oberti C; Sterba R; Marangi D; Tchou PJ; Chung MK; Wang Q
    Clin Genet; 2003 Apr; 63(4):273-82. PubMed ID: 12702160
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Long QT Syndrome.
    Vohra J
    Heart Lung Circ; 2007; 16 Suppl 3():S5-12. PubMed ID: 17627884
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Molecular biology of the long QT syndrome: impact on management.
    Priori SG; Napolitano C; Paganini V; Cantù F; Schwartz PJ
    Pacing Clin Electrophysiol; 1997 Aug; 20(8 Pt 2):2052-7. PubMed ID: 9272507
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.