242 related articles for article (PubMed ID: 11332568)
1. Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family members.
Kaufman ES; Priori SG; Napolitano C; Schwartz PJ; Iyengar S; Elston RC; Schnell AH; Gorodeski EZ; Rammohan G; Bahhur NO; Connuck D; Verrilli L; Rosenbaum DS; Brown AM
J Cardiovasc Electrophysiol; 2001 Apr; 12(4):455-61. PubMed ID: 11332568
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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; Baró I; Touboul P
Cardiovasc Res; 2001 May; 50(2):386-98. PubMed ID: 11334843
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. [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]
10. Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns.
Piippo K; Laitinen P; Swan H; Toivonen L; Viitasalo M; Pasternack M; Paavonen K; Chapman H; Wann KT; Hirvelä E; Sajantila A; Kontula K
J Am Coll Cardiol; 2000 Jun; 35(7):1919-25. PubMed ID: 10841244
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
Wong JA; Gula LJ; Klein GJ; Yee R; Skanes AC; Krahn AD
Circ Arrhythm Electrophysiol; 2010 Apr; 3(2):120-5. PubMed ID: 20071715
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. An intronic mutation causes long QT syndrome.
Zhang L; Vincent GM; Baralle M; Baralle FE; Anson BD; Benson DW; Whiting B; Timothy KW; Carlquist J; January CT; Keating MT; Splawski I
J Am Coll Cardiol; 2004 Sep; 44(6):1283-91. PubMed ID: 15364333
[TBL] [Abstract][Full Text] [Related]
19. Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome.
Satler CA; Vesely MR; Duggal P; Ginsburg GS; Beggs AH
Hum Genet; 1998 Mar; 102(3):265-72. PubMed ID: 9544837
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
