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Items: 1 to 20 of 72

1.

Beat-to-beat repolarization variability in amplitude and duration in LQTS patients with the SCN5A sodium channel gene mutation.

Couderc JP, Zareba W, Burattini L, Konecki JA, Moss AJ.

J Electrocardiol. 1998;31 Suppl:134. No abstract available.

PMID:
9988018
2.

Beat-to-Beat repolarization variability in LQTS patients with the SCN5A sodium channel gene mutation.

Couderc JP, Zareba W, Burattini L, Moss AJ.

Pacing Clin Electrophysiol. 1999 Nov;22(11):1581-92.

PMID:
10598960
3.

Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation.

Windle JR, Geletka RC, Moss AJ, Zareba W, Atkins DL.

Ann Noninvasive Electrocardiol. 2001 Apr;6(2):153-8.

PMID:
11333173
4.

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

Abriel H, Cabo C, Wehrens XH, Rivolta I, Motoike HK, Memmi M, Napolitano C, Priori SG, Kass RS.

Circ Res. 2001 Apr 13;88(7):740-5.

5.

Beat-to-beat T-wave amplitude variability in the long QT syndrome.

Extramiana F, Tatar C, Maison-Blanche P, Denjoy I, Messali A, Dejode P, Iserin F, Leenhardt A.

Europace. 2010 Sep;12(9):1302-7. doi: 10.1093/europace/euq137. Epub 2010 May 14. Erratum in: Europace. 2011 Mar;13(3):450.

PMID:
20472689
6.
7.

Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome.

Antzelevitch C, Yan GX, Shimizu W.

J Electrocardiol. 1999;32 Suppl:158-65. Review.

PMID:
10688320
8.

Congenital long QT syndrome and 2:1 atrioventricular block with a mutation of the SCN5A gene.

Miura M, Yamagishi H, Morikawa Y, Matsuoka R.

Pediatr Cardiol. 2003 Jan-Feb;24(1):70-2.

PMID:
12574983
9.

Altered atrial, atrioventricular, and ventricular conduction in patients with the long QT syndrome caused by the DeltaKPQ SCN5A sodium channel gene mutation.

Zareba W, Sattari MN, Rosero S, Couderc JP, Moss AJ.

Am J Cardiol. 2001 Dec 1;88(11):1311-4. No abstract available.

PMID:
11728364
10.

Heart rate variability in patients with congenital long QT syndrome.

Perkiömäki JS, Zareba W, Couderc JP, Moss AJ.

Ann Noninvasive Electrocardiol. 2001 Oct;6(4):298-304.

PMID:
11686910
11.

Effects of flecainide in patients with new SCN5A mutation: mutation-specific therapy for long-QT syndrome?

Benhorin J, Taub R, Goldmit M, Kerem B, Kass RS, Windman I, Medina A.

Circulation. 2000 Apr 11;101(14):1698-706.

12.

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.

Vatta M, Ackerman MJ, Ye B, Makielski JC, Ughanze EE, Taylor EW, Tester DJ, Balijepalli RC, Foell JD, Li Z, Kamp TJ, Towbin JA.

Circulation. 2006 Nov 14;114(20):2104-12. Epub 2006 Oct 23.

13.

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.

Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JP, Fressart V, Guicheney P, Chahine M.

J Mol Cell Cardiol. 2003 Dec;35(12):1513-21.

PMID:
14654377
14.

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.

Wang DW, Yazawa K, George AL Jr, Bennett PB.

Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13200-5.

15.

Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations.

Wattanasirichaigoon D, Vesely MR, Duggal P, Levine JC, Blume ED, Wolff GS, Edwards SB, Beggs AH.

Am J Med Genet. 1999 Oct 29;86(5):470-6.

PMID:
10508990
16.

T-wave patterns associated with the hereditary long QT syndrome.

Moss AJ.

Card Electrophysiol Rev. 2002 Sep;6(3):311-5. Review.

PMID:
12114857
17.

A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.

Groenewegen WA, Bezzina CR, van Tintelen JP, Hoorntje TM, Mannens MM, Wilde AA, Jongsma HJ, Rook MB.

Cardiovasc Res. 2003 Mar 15;57(4):1072-8.

PMID:
12650885
18.

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 15;94(10):1312-6.

PMID:
15541256
19.

Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular block.

Lupoglazoff JM, Cheav T, Baroudi G, Berthet M, Denjoy I, Cauchemez B, Extramiana F, Chahine M, Guicheney P.

Circ Res. 2001 Jul 20;89(2):E16-21.

20.

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