232 related articles for article (PubMed ID: 9973011)
1. Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).
Wilde AA; Jongbloed RJ; Doevendans PA; Düren DR; Hauer RN; van Langen IM; van Tintelen JP; Smeets HJ; Meyer H; Geelen JL
J Am Coll Cardiol; 1999 Feb; 33(2):327-32. PubMed ID: 9973011
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
Moss AJ; Zareba W; Kaufman ES; Gartman E; Peterson DR; Benhorin J; Towbin JA; Keating MT; Priori SG; Schwartz PJ; Vincent GM; Robinson JL; Andrews ML; Feng C; Hall WJ; Medina A; Zhang L; Wang Z
Circulation; 2002 Feb; 105(7):794-9. PubMed ID: 11854117
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
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. Familial and acquired long qt syndrome and the cardiac rapid delayed rectifier potassium current.
Witchel HJ; Hancox JC
Clin Exp Pharmacol Physiol; 2000 Oct; 27(10):753-66. PubMed ID: 11022966
[TBL] [Abstract][Full Text] [Related]
17. Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.
Yoshida H; Horie M; Otani H; Kawashima T; Onishi Y; Sasayama S
Am J Med Genet; 2001 Feb; 98(4):348-52. PubMed ID: 11170080
[TBL] [Abstract][Full Text] [Related]
18. Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome.
Tanaka T; Nagai R; Tomoike H; Takata S; Yano K; Yabuta K; Haneda N; Nakano O; Shibata A; Sawayama T; Kasai H; Yazaki Y; Nakamura Y
Circulation; 1997 Feb; 95(3):565-7. PubMed ID: 9024139
[TBL] [Abstract][Full Text] [Related]
19. Cellular consequences of HERG mutations in the long QT syndrome: precursors to sudden cardiac death.
Clancy CE; Rudy Y
Cardiovasc Res; 2001 May; 50(2):301-13. PubMed ID: 11334834
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
