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Items: 1 to 20 of 114

1.

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.

2.

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.

Van Langen IM, Birnie E, Alders M, Jongbloed RJ, Le Marec H, Wilde AA.

J Med Genet. 2003 Feb;40(2):141-5. No abstract available.

3.

Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.

Allan WC, Timothy K, Vincent GM, Palomaki GE, Neveux LM, Haddow JE.

J Med Screen. 2001;8(4):173-7.

PMID:
11743032
4.
5.

[Genetic background predisposing the drug-induced long QT syndrome].

Horie M.

Nihon Yakurigaku Zasshi. 2003 Jun;121(6):401-7. Review. Japanese.

PMID:
12835534
6.

Cardiac arrhythmias: the genetic connection.

Towbin JA.

J Cardiovasc Electrophysiol. 2000 May;11(5):601-2. Review. No abstract available.

PMID:
10826942
7.

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
8.

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous.

Schulze-Bahr E, Haverkamp W, Wedekind H, Rubie C, Hördt M, Borggrefe M, Assmann G, Breithardt G, Funke H.

Hum Genet. 1997 Oct;100(5-6):573-6.

PMID:
9341873
9.

Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions.

Syrris P, Murray A, Carter ND, McKenna WM, Jeffery S.

J Med Genet. 2001 Oct;38(10):705-10. No abstract available.

10.
11.

The long QT syndromes: genetic basis and clinical implications.

Chiang CE, Roden DM.

J Am Coll Cardiol. 2000 Jul;36(1):1-12. Review.

12.

Congenital and acquired long QT syndrome.

Camm AJ, Janse MJ, Roden DM, Rosen MR, Cinca J, Cobbe SM.

Eur Heart J. 2000 Aug;21(15):1232-7. Review. No abstract available.

13.

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.

14.

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
15.

Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome.

Liu W, Hu D, Li C, Li P, Li Y, Li Z, Li L, Qin X, Dong W, Qi Y, Chen S, Wang Q.

Chin Med J (Engl). 2003 Sep;116(9):1333-5.

PMID:
14527360
16.

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
17.

[Etiological mechanism of long QT syndrome and the effects of macrolides].

Kato T.

Jpn J Antibiot. 2001 Feb;54 Suppl A:118-22. Japanese. No abstract available.

PMID:
11439888
18.

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.

19.

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.

Yang P, Kanki H, Drolet B, Yang T, Wei J, Viswanathan PC, Hohnloser SH, Shimizu W, Schwartz PJ, Stanton M, Murray KT, Norris K, George AL Jr, Roden DM.

Circulation. 2002 Apr 23;105(16):1943-8.

20.

Genotype and severity of long QT syndrome.

Towbin JA, Wang Z, Li H.

Arch Pathol Lab Med. 2001 Jan;125(1):116-21. Review.

PMID:
11151064
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