130 related articles for article (PubMed ID: 16678140)
1. Low penetrance, subclinical congenital LQTS: concealed LQTS or silent LQTS?
Varró A; Papp JG
Cardiovasc Res; 2006 Jun; 70(3):404-6. PubMed ID: 16678140
[No Abstract] [Full Text] [Related]
2. Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
Ohno S; Toyoda F; Zankov DP; Yoshida H; Makiyama T; Tsuji K; Honda T; Obayashi K; Ueyama H; Shimizu W; Miyamoto Y; Kamakura S; Matsuura H; Kita T; Horie M
Hum Mutat; 2009 Apr; 30(4):557-63. PubMed ID: 19306396
[TBL] [Abstract][Full Text] [Related]
3. Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndrome.
Oka Y; Itoh H; Ding WG; Shimizu W; Makiyama T; Ohno S; Nishio Y; Sakaguchi T; Miyamoto A; Kawamura M; Matsuura H; Horie M
Circ J; 2010 Nov; 74(12):2562-71. PubMed ID: 20975234
[TBL] [Abstract][Full Text] [Related]
4. Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointes.
Lehtonen A; Fodstad H; Laitinen-Forsblom P; Toivonen L; Kontula K; Swan H
Heart Rhythm; 2007 May; 4(5):603-7. PubMed ID: 17467628
[TBL] [Abstract][Full Text] [Related]
5. The role of abnormal trafficking of KCNE1 in long QT syndrome 5.
Harmer SC; Tinker A
Biochem Soc Trans; 2007 Nov; 35(Pt 5):1074-6. PubMed ID: 17956282
[TBL] [Abstract][Full Text] [Related]
6. Giant T-U waves precede torsades de pointes in long QT syndrome: a systematic electrocardiographic analysis in patients with acquired and congenital QT prolongation.
Kirchhof P; Franz MR; Bardai A; Wilde AM
J Am Coll Cardiol; 2009 Jul; 54(2):143-9. PubMed ID: 19573731
[TBL] [Abstract][Full Text] [Related]
7. Gene mutations associated with atrioventricular block complicated by long QT syndrome.
Nishizaki M; Hiraoka M
Circ J; 2010 Nov; 74(12):2546-7. PubMed ID: 21088333
[No Abstract] [Full Text] [Related]
8. Temporal repolarization lability differences among genotyped patients with the long QT syndrome.
Bilchick K; Viitasalo M; Oikarinen L; Fetics B; Tomaselli G; Swan H; Laitinen PJ; Väänänen H; Kontula K; Berger RD
Am J Cardiol; 2004 Nov; 94(10):1312-6. PubMed ID: 15541256
[TBL] [Abstract][Full Text] [Related]
9. Congenital and acquired long QT syndromes.
Walker BD; Krahn AD; Klein GJ; Skanes AC; Wang J; Hegele RA; Yee R
Can J Cardiol; 2003 Jan; 19(1):76-87. PubMed ID: 12571698
[TBL] [Abstract][Full Text] [Related]
10. Dangerous and life-threatening drugs - practical lessons from the long QT syndrome.
Schutte D; Obel W
Cardiovasc J S Afr; 2002; 13(2):54-61. PubMed ID: 11981581
[TBL] [Abstract][Full Text] [Related]
11. Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 gene.
Tsuji K; Akao M; Ishii TM; Ohno S; Makiyama T; Takenaka K; Doi T; Haruna Y; Yoshida H; Nakashima T; Kita T; Horie M
J Mol Cell Cardiol; 2007 Mar; 42(3):662-9. PubMed ID: 17292394
[TBL] [Abstract][Full Text] [Related]
12. Revised definition of M cell and torsade de pointes in long QT syndrome.
Takahashi N
J Cardiovasc Electrophysiol; 2005 Sep; 16(9):988-90. PubMed ID: 16174021
[No Abstract] [Full Text] [Related]
13. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
[TBL] [Abstract][Full Text] [Related]
14. Phenotype reveals genotype in a Greek long QT syndrome family.
Anastasakis A; Kotta CM; Kyriakogonas S; Wollnik B; Theopistou A; Stefanadis C
Europace; 2006 Apr; 8(4):241-4. PubMed ID: 16627448
[TBL] [Abstract][Full Text] [Related]
15. Functional suppression of Kcnq1 leads to early sodium channel remodelling and cardiac conduction system dysmorphogenesis.
de la Rosa AJ; Domínguez JN; Sedmera D; Sankova B; Hove-Madsen L; Franco D; Aránega AE
Cardiovasc Res; 2013 Jun; 98(3):504-14. PubMed ID: 23542581
[TBL] [Abstract][Full Text] [Related]
16. Long QT syndrome in adults.
Sauer AJ; Moss AJ; McNitt S; Peterson DR; Zareba W; Robinson JL; Qi M; Goldenberg I; Hobbs JB; Ackerman MJ; Benhorin J; Hall WJ; Kaufman ES; Locati EH; Napolitano C; Priori SG; Schwartz PJ; Towbin JA; Vincent GM; Zhang L
J Am Coll Cardiol; 2007 Jan; 49(3):329-37. PubMed ID: 17239714
[TBL] [Abstract][Full Text] [Related]
17. Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes.
Mank-Seymour AR; Richmond JL; Wood LS; Reynolds JM; Fan YT; Warnes GR; Milos PM; Thompson JF
Am Heart J; 2006 Dec; 152(6):1116-22. PubMed ID: 17161064
[TBL] [Abstract][Full Text] [Related]
18. The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes.
Li W; Du R; Wang QF; Tian L; Yang JG; Song ZF
Biochem Biophys Res Commun; 2009 May; 383(2):206-9. PubMed ID: 19348785
[TBL] [Abstract][Full Text] [Related]
19. Early afterdepolarizations, U waves, and torsades de pointes.
Wu J; Wu J; Zipes DP
Circulation; 2002 Feb; 105(6):675-6. PubMed ID: 11839619
[No Abstract] [Full Text] [Related]
20. Congenital long QT syndrome caused by the F275S KCNQ1 mutation: mechanism of impaired channel function.
Li W; Wang QF; Du R; Xu QM; Ke QM; Wang B; Chen XL; Tian L; Zhang SY; Kang CL; Guan SM; Yang JG; Song ZF
Biochem Biophys Res Commun; 2009 Feb; 380(1):127-31. PubMed ID: 19167356
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
