PubMed

Congenital long QT syndrome.

Crotti L, Celano G, Dagradi F, Schwartz PJ.

Orphanet J Rare Dis. 2008 Jul 7;3:18. Review.PMID: 18606002 [PubMed - indexed for MEDLINE]Related articlesFree article

[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. Chinese. PMID: 16831322 [PubMed - indexed for MEDLINE]Related articles

Congenital and acquired long QT syndrome. Current concepts and management.

Chiang CE.

Cardiol Rev. 2004 Jul-Aug;12(4):222-34. Review.PMID: 15191637 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 12442276 [PubMed - indexed for MEDLINE]Related articlesFree article

[Molecular genetics in the hereditary form of long QT syndrome]

Georgijević Milić L.

Med Pregl. 2000 Jan-Feb;53(1-2):51-4. Review. Croatian. PMID: 10953551 [PubMed - indexed for MEDLINE]Related articles

[A novel KCNQ1 mutation in Chinese with congenital long QT syndrome]

Liang L, Du ZD, Cai LL, Wu JX, Zheng T, Qi TX.

Zhonghua Er Ke Za Zhi. 2003 Oct;41(10):724-7. Chinese. PMID: 14731347 [PubMed - indexed for MEDLINE]Related articles

KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.

Chen S, Zhang L, Bryant RM, Vincent GM, Flippin M, Lee JC, Brown E, Zimmerman F, Rozich R, Szafranski P, Oberti C, Sterba R, Marangi D, Tchou PJ, Chung MK, Wang Q.

Clin Genet. 2003 Apr;63(4):273-82.PMID: 12702160 [PubMed - indexed for MEDLINE]Related articlesFree article

[Value of genetic testing in the management of the congenital long QT syndrome]

Lupoglazoff JM, Denjoy I, Guicheney P.

Arch Mal Coeur Vaiss. 2003 May;96(5):539-47. Review. French. PMID: 12838849 [PubMed - indexed for MEDLINE]Related articles

The inherited long QT syndrome: from ion channel to bedside.

Vincent GM, Timothy K, Fox J, Zhang L.

Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Review.PMID: 10348966 [PubMed - indexed for MEDLINE]Related articles

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.PMID: 11781953 [PubMed - indexed for MEDLINE]Related articles

[Molecular genetics of the long QT syndrome: clinical aspects]

Sepp R, Csanády M.

Orv Hetil. 1999 Nov 21;140(47):2633-8. Review. Hungarian. PMID: 10613047 [PubMed - indexed for MEDLINE]Related articles

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.

Tester DJ, Will ML, Haglund CM, Ackerman MJ.

Heart Rhythm. 2005 May;2(5):507-17.PMID: 15840476 [PubMed - indexed for MEDLINE]Related articles

Long QT syndrome and short QT syndrome.

Zareba W, Cygankiewicz I.

Prog Cardiovasc Dis. 2008 Nov-Dec;51(3):264-78. Review.PMID: 19026859 [PubMed - indexed for MEDLINE]Related articles

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.

Vincent GM.

Annu Rev Med. 1998;49:263-74. Review.PMID: 9509262 [PubMed - indexed for MEDLINE]Related articles

Long QT and Brugada syndrome gene mutations in New Zealand.

Chung SK, MacCormick JM, McCulley CH, Crawford J, Eddy CA, Mitchell EA, Shelling AN, French JK, Skinner JR, Rees MI.

Heart Rhythm. 2007 Oct;4(10):1306-14. Epub 2007 Jul 14.PMID: 17905336 [PubMed - indexed for MEDLINE]Related articles

[The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome]

Denjoy I, Lupoglazoff JM, Villain E, Vaksmann G, Godart F, Lucet V, Leenhardt A, Guicheney P, Schwartz P.

Arch Mal Coeur Vaiss. 2007 May;100(5):359-64. French. PMID: 17646758 [PubMed - indexed for MEDLINE]Related articles

Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.

Horigome H, Nagashima M, Sumitomo N, Yoshinaga M, Ushinohama H, Iwamoto M, Shiono J, Ichihashi K, Hasegawa S, Yoshikawa T, Matsunaga T, Goto H, Waki K, Arima M, Takasugi H, Tanaka Y, Tauchi N, Ikoma M, Inamura N, Takahashi H, Shimizu W, Horie M.

Circ Arrhythm Electrophysiol. 2010 Feb 1;3(1):10-7. Epub 2009 Dec 8.PMID: 19996378 [PubMed - indexed for MEDLINE]Related articles

Molecular biology of the long QT syndrome: impact on management.

Priori SG, Napolitano C, Paganini V, Cantù F, Schwartz PJ.

Pacing Clin Electrophysiol. 1997 Aug;20(8 Pt 2):2052-7. Review.PMID: 9272507 [PubMed - indexed for MEDLINE]Related articles

Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.

Tester DJ, Cronk LB, Carr JL, Schulz V, Salisbury BA, Judson RS, Ackerman MJ.

Heart Rhythm. 2006 Jul;3(7):815-21. Epub 2006 Mar 16.PMID: 16818214 [PubMed - indexed for MEDLINE]Related articles

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.

Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Wang DW, Rhodes TE, George AL Jr, Schwartz PJ.

Circulation. 2007 Jan 23;115(3):361-7. Epub 2007 Jan 8.PMID: 17210839 [PubMed - indexed for MEDLINE]Related articlesFree article