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Items: 1 to 20 of 170

1.

Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.

Benhorin J, Moss AJ, Bak M, Zareba W, Kaufman ES, Kerem B, Towbin JA, Priori S, Kass RS, Attali B, Brown AM, Ficker E.

Ann Noninvasive Electrocardiol. 2002 Jan;7(1):40-6.

PMID:
11844290
2.

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, Schwartz PJ, Vincent GM, Priori SG, Benhorin J, Towbin JA, Robinson JL, Andrews ML, Napolitano C, Timothy K, Zhang L, Medina A; International Long QT Syndrome Registry..

J Am Coll Cardiol. 2003 Jul 2;42(1):103-9.

3.

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns.

Piippo K, Laitinen P, Swan H, Toivonen L, Viitasalo M, Pasternack M, Paavonen K, Chapman H, Wann KT, Hirvelä E, Sajantila A, Kontula K.

J Am Coll Cardiol. 2000 Jun;35(7):1919-25.

4.

Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family members.

Kaufman ES, Priori SG, Napolitano C, Schwartz PJ, Iyengar S, Elston RC, Schnell AH, Gorodeski EZ, Rammohan G, Bahhur NO, Connuck D, Verrilli L, Rosenbaum DS, Brown AM.

J Cardiovasc Electrophysiol. 2001 Apr;12(4):455-61.

PMID:
11332568
5.

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.

Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z.

Circulation. 2002 Feb 19;105(7):794-9.

6.

Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.

Lupoglazoff JM, Denjoy I, Berthet M, Neyroud N, Demay L, Richard P, Hainque B, Vaksmann G, Klug D, Leenhardt A, Maillard G, Coumel P, Guicheney P.

Circulation. 2001 Feb 27;103(8):1095-101.

7.

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.

Jongbloed RJ, Wilde AA, Geelen JL, Doevendans P, Schaap C, Van Langen I, van Tintelen JP, Cobben JM, Beaufort-Krol GC, Geraedts JP, Smeets HJ.

Hum Mutat. 1999;13(4):301-10.

PMID:
10220144
8.
9.

Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.

Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Mabuchi H.

Circ J. 2003 Jun;67(6):495-8.

10.

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.

11.

Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome.

Satler CA, Vesely MR, Duggal P, Ginsburg GS, Beggs AH.

Hum Genet. 1998 Mar;102(3):265-72.

PMID:
9544837
12.

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
13.
14.

Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related Gene.

Roti EC, Myers CD, Ayers RA, Boatman DE, Delfosse SA, Chan EK, Ackerman MJ, January CT, Robertson GA.

J Biol Chem. 2002 Dec 6;277(49):47779-85. Epub 2002 Sep 20.

15.

Identical twins with long QT syndrome associated with a missense mutation in the S4 region of the HERG.

Hayashi K, Shimizu M, Ino H, Okeie K, Yamaguchi M, Yasuda T, Fujino N, Fujii H, Fujita S, Mabuchi H.

Jpn Heart J. 2000 May;41(3):399-404.

16.

Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.

Isbrandt D, Friederich P, Solth A, Haverkamp W, Ebneth A, Borggrefe M, Funke H, Sauter K, Breithardt G, Pongs O, Schulze-Bahr E.

J Mol Med (Berl). 2002 Aug;80(8):524-32. Epub 2002 Jun 28.

PMID:
12185453
17.

Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome.

Moennig G, Schulze-Bahr E, Wedekind H, Borggrefe M, Funke H, Toelle M, Kirchhof P, Eckardt L, Assmann G, Breithardt G, Haverkamp W.

Pacing Clin Electrophysiol. 2001 Apr;24(4 Pt 1):406-15.

PMID:
11341076
18.

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome.

Tanaka T, Nagai R, Tomoike H, Takata S, Yano K, Yabuta K, Haneda N, Nakano O, Shibata A, Sawayama T, Kasai H, Yazaki Y, Nakamura Y.

Circulation. 1997 Feb 4;95(3):565-7.

19.

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.

Berthet M, Denjoy I, Donger C, Demay L, Hammoude H, Klug D, Schulze-Bahr E, Richard P, Funke H, Schwartz K, Coumel P, Hainque B, Guicheney P.

Circulation. 1999 Mar 23;99(11):1464-70.

20.

Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel.

Huang FD, Chen J, Lin M, Keating MT, Sanguinetti MC.

Circulation. 2001 Aug 28;104(9):1071-5.

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