154 related articles for article (PubMed ID: 22706706)
41. Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome.
Yang T; Chung SK; Zhang W; Mullins JG; McCulley CH; Crawford J; MacCormick J; Eddy CA; Shelling AN; French JK; Yang P; Skinner JR; Roden DM; Rees MI
Circ Arrhythm Electrophysiol; 2009 Aug; 2(4):417-26. PubMed ID: 19808498
[TBL] [Abstract][Full Text] [Related]
42. [Clinical care for patients with possible long QT syndrome].
Hayano M
Nihon Naika Gakkai Zasshi; 2006 Feb; 95(2):314-9. PubMed ID: 16536083
[No Abstract] [Full Text] [Related]
43. Current Indications for Implantable Cardioverter Defibrillators in Non-Ischemic Cardiomyopathies and Channelopathies.
González-Torrecilla E; Arenal A; Atienza F; Datino T; Bravo L; Ruiz P; Ávila P; Fernández-Avilés F
Rev Recent Clin Trials; 2015; 10(2):111-27. PubMed ID: 25845953
[TBL] [Abstract][Full Text] [Related]
44. Congenital long QT syndrome presenting with a history of epilepsy: misdiagnosis or relationship between channelopathies of the heart and brain?
Omichi C; Momose Y; Kitahara S
Epilepsia; 2010 Feb; 51(2):289-92. PubMed ID: 19694797
[TBL] [Abstract][Full Text] [Related]
45. Septal hypertrabeculation/noncompaction: cardiac and neurologic implications.
Stöllberger C; Finsterer J
Int J Cardiol; 2009 Feb; 132(2):173-5. PubMed ID: 19046611
[TBL] [Abstract][Full Text] [Related]
46. Long QT Syndrome Type 1 in an Australian Indigenous Patient.
Ganesan AN; Vanoye CG; Alam F; Waddell-Smith KE; McGavigan AD; Correnti G; Haan E; Brown A; Vandenberg J; George AL
Circ Genom Precis Med; 2020 Apr; 13(2):e002813. PubMed ID: 32004091
[No Abstract] [Full Text] [Related]
47. Is there a role for implantable cardioverter defibrillators in long QT syndrome?
Welde AA
J Cardiovasc Electrophysiol; 2002 Jan; 13(1 Suppl):S110-3. PubMed ID: 11852886
[TBL] [Abstract][Full Text] [Related]
48. [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]
49. 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]
50. 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]
51. Novel gene and mutation discovery in congenital long QT syndrome: let's keep looking where the street lamp standeth.
Tester DJ; Ackerman MJ
Heart Rhythm; 2008 Sep; 5(9):1282-4. PubMed ID: 18774103
[No Abstract] [Full Text] [Related]
52. Inherited long QT syndrome: phenotype and therapy to use and avoid.
Conti CR
Clin Cardiol; 2006 Oct; 29(10):429-30. PubMed ID: 17063944
[TBL] [Abstract][Full Text] [Related]
53. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322
[TBL] [Abstract][Full Text] [Related]
54. Mutation of an A-kinase-anchoring protein causes long-QT syndrome.
Chen L; Marquardt ML; Tester DJ; Sampson KJ; Ackerman MJ; Kass RS
Proc Natl Acad Sci U S A; 2007 Dec; 104(52):20990-5. PubMed ID: 18093912
[TBL] [Abstract][Full Text] [Related]
55. Long QT and Brugada syndromes: from genetics to clinical management.
Priori SG
J Cardiovasc Electrophysiol; 2000 Oct; 11(10):1174-8. PubMed ID: 11059984
[No Abstract] [Full Text] [Related]
56. Counting mRNA in blood of LQTS - new direction?
Zaręba W
Kardiol Pol; 2011; 69(5):430. PubMed ID: 21594823
[No Abstract] [Full Text] [Related]
57. 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]
58. [Why do we need genetics in cardiac rhythmology?].
Rieder M; Castiglione A; Asatryan B; Odening KE
Herzschrittmacherther Elektrophysiol; 2020 Dec; 31(4):394-400. PubMed ID: 32661562
[TBL] [Abstract][Full Text] [Related]
59. Ion channel complex disease in long QT syndrome.
Morita H
Heart Rhythm; 2013 May; 10(5):738-9. PubMed ID: 23354076
[No Abstract] [Full Text] [Related]
60. Cardiac channelopathies and sudden infant death syndrome.
Tfelt-Hansen J; Winkel BG; Grunnet M; Jespersen T
Cardiology; 2011; 119(1):21-33. PubMed ID: 21778721
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]