91 related articles for article (PubMed ID: 20960619)
1. Gene symbol: KCNQ1. Disease: Long QT syndrome.
Crotti L; Ferrandi C; Pedrazzini M; Insolia R; Cuoretti A; Celano G; Dagradi F; Stramba-Badiale M; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):543. PubMed ID: 20960619
[No Abstract] [Full Text] [Related]
2. Gene symbol: KCNQ1. Disease: Long QT syndrome.
Crotti L; Insolia R; Ferrandi C; Pedrazzini M; Cuoretti A; Gandolfi E; Sanzo A; Dagradi F; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):541. PubMed ID: 20960614
[No Abstract] [Full Text] [Related]
3. 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]
4. Gene symbol: KCNQ1. Disease: LQT1.
Arbustini E; Diegoli M; Pasotti M; Grasso M; Marziliano N; Marini M; Zeni P; Disertori M
Hum Genet; 2006 Jul; 119(6):682. PubMed ID: 17128491
[No Abstract] [Full Text] [Related]
5. [T-wave variability in the long QT syndrome].
Zienciuk A; Potaz P; Morzuch L; Kwiatkowska J
Kardiol Pol; 2008 Sep; 66(9):995-6; discussion 997-8. PubMed ID: 18924032
[No Abstract] [Full Text] [Related]
6. Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L; Pedrazzini M; Ferrandi C; Insolia R; Cuoretti A; Dagradi F; Crimi G; Coto E; Reguero JR; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):543. PubMed ID: 20960620
[No Abstract] [Full Text] [Related]
7. [Atrial fibrillation in the long QT syndrome].
Zienciuk A; Szwoch M; Raczak G
Kardiol Pol; 2009 Jun; 67(6):681-4, discussion 685-6. PubMed ID: 19618328
[TBL] [Abstract][Full Text] [Related]
8. Long QT syndrome in children: not one disease anymore.
Balaji S
J Am Coll Cardiol; 2007 Oct; 50(14):1341-2. PubMed ID: 17903633
[No Abstract] [Full Text] [Related]
9. Gene symbol: KCNQ1.
Crotti L; Insolia R; Pedrazzini M; Ferrandi C; Tosin L; Moncalvo C; Turco A; Agnetti A; De Ferrari GM; Schwartz PJ
Hum Genet; 2007 Feb; 120(6):912. PubMed ID: 17438609
[No Abstract] [Full Text] [Related]
10. [Mutation analysis of a Chinese family with inherited long QT syndrome].
Du R; Yang JG; Li W; Gui L; Yuan GH; Kang CL; Ren FX; Zhang SY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):68-70. PubMed ID: 15696484
[TBL] [Abstract][Full Text] [Related]
11. Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families.
Amirian A; Zafari Z; Karimipoor M; Kordafshari A; Dalili M; Saber S; Farjam Fazelifar A; Zeinali S
Iran Biomed J; 2019 May; 23(3):228-34. PubMed ID: 30797226
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.
Wei J; Fish FA; Myerburg RJ; Roden DM; George AL
Hum Mutat; 2000 Apr; 15(4):387-8. PubMed ID: 10737999
[TBL] [Abstract][Full Text] [Related]
14. Presentation and outcome of water-related events in children with long QT syndrome.
Albertella L; Crawford J; Skinner JR
Arch Dis Child; 2011 Aug; 96(8):704-7. PubMed ID: 21131640
[No Abstract] [Full Text] [Related]
15. 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]
16. [Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning].
Correia MJ
Rev Port Cardiol; 2000 Feb; 19(2):275-6. PubMed ID: 10763359
[No Abstract] [Full Text] [Related]
17. Novel mutations of KCNQ1 in Long QT syndrome.
Qureshi SF; Ali A; Ananthapur V; Jayakrishnan MP; Calambur N; Thangaraj K; Nallari P
Indian Heart J; 2013; 65(5):552-60. PubMed ID: 24206879
[TBL] [Abstract][Full Text] [Related]
18. Gene symbol: SCN5A.
Crotti L; Ferrandi C; Insolia R; Pedrazzini M; Andreoli E; Veia A; Crimi G; Agnetti A; De Ferrari GM; Schwartz PJ
Hum Genet; 2007 Feb; 120(6):913. PubMed ID: 17438610
[No Abstract] [Full Text] [Related]
19. Beta1-adrenergic receptor polymorphisms, QTc interval and occurrence of symptoms in type 1 of long QT syndrome.
Paavonen KJ; Swan H; Piippo K; Laitinen P; Fodstad H; Sarna S; Toivonen L; Kontula K; Viitasalo M
Int J Cardiol; 2007 May; 118(2):197-202. PubMed ID: 17023080
[TBL] [Abstract][Full Text] [Related]
20. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Mabuchi H; Hoshi N; Higashida H
Clin Sci (Lond); 2003 Apr; 104(4):377-82. PubMed ID: 12653681
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
