574 related articles for article (PubMed ID: 11997281)
1. Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.
Yang P; Kanki H; Drolet B; Yang T; Wei J; Viswanathan PC; Hohnloser SH; Shimizu W; Schwartz PJ; Stanton M; Murray KT; Norris K; George AL; Roden DM
Circulation; 2002 Apr; 105(16):1943-8. PubMed ID: 11997281
[TBL] [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. [Genetic background predisposing the drug-induced long QT syndrome].
Horie M
Nihon Yakurigaku Zasshi; 2003 Jun; 121(6):401-7. PubMed ID: 12835534
[TBL] [Abstract][Full Text] [Related]
4. 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; 82(3):182-8. PubMed ID: 14760488
[TBL] [Abstract][Full Text] [Related]
5. QT interval prolongation and cardiac risk assessment for novel drugs.
Picard S; Lacroix P
Curr Opin Investig Drugs; 2003 Mar; 4(3):303-8. PubMed ID: 12735231
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. [Etiological mechanism of long QT syndrome and the effects of macrolides].
Kato T
Jpn J Antibiot; 2001 Feb; 54 Suppl A():118-22. PubMed ID: 11439888
[No Abstract] [Full Text] [Related]
15. 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]
16. Modulation of HERG potassium channels by extracellular magnesium and quinidine.
Po SS; Wang DW; Yang IC; Johnson JP; Nie L; Bennett PB
J Cardiovasc Pharmacol; 1999 Feb; 33(2):181-5. PubMed ID: 10028924
[TBL] [Abstract][Full Text] [Related]
17. Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.
Sanguinetti MC
Ann N Y Acad Sci; 1999 Apr; 868():406-13. PubMed ID: 10414310
[TBL] [Abstract][Full Text] [Related]
18. Cardiac repolarization: current knowledge, critical gaps, and new approaches to drug development and patient management.
Anderson ME; Al-Khatib SM; Roden DM; Califf RM;
Am Heart J; 2002 Nov; 144(5):769-81. PubMed ID: 12422144
[No Abstract] [Full Text] [Related]
19. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
Splawski I; Shen J; Timothy KW; Vincent GM; Lehmann MH; Keating MT
Genomics; 1998 Jul; 51(1):86-97. PubMed ID: 9693036
[TBL] [Abstract][Full Text] [Related]
20. Cardiac arrhythmias: the genetic connection.
Towbin JA
J Cardiovasc Electrophysiol; 2000 May; 11(5):601-2. PubMed ID: 10826942
[No Abstract] [Full Text] [Related]
[Next] [New Search]