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Items: 1 to 20 of 86

1.

Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome.

Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T.

J Hum Genet. 2001;46(1):38-40.

PMID:
11289718
2.

Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.

Kobori A, Sarai N, Shimizu W, Nakamura Y, Murakami Y, Makiyama T, Ohno S, Takenaka K, Ninomiya T, Fujiwara Y, Matsuoka S, Takano M, Noma A, Kita T, Horie M.

J Cardiovasc Electrophysiol. 2004 Feb;15(2):190-9.

PMID:
15028050
3.

Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome.

Villain E, Denjoy I, Lupoglazoff JM, Guicheney P, Hainque B, Lucet V, Bonnet D.

Eur Heart J. 2004 Aug;25(16):1405-11.

PMID:
15321698
4.

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.

Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT.

Circulation. 2000 Sep 5;102(10):1178-85.

5.

Long QT syndrome in children in the era of implantable defibrillators.

Etheridge SP, Sanatani S, Cohen MI, Albaro CA, Saarel EV, Bradley DJ.

J Am Coll Cardiol. 2007 Oct 2;50(14):1335-40. Epub 2007 Sep 17.

6.

Long QT syndrome in adults.

Sauer AJ, Moss AJ, McNitt S, Peterson DR, Zareba W, Robinson JL, Qi M, Goldenberg I, Hobbs JB, Ackerman MJ, Benhorin J, Hall WJ, Kaufman ES, Locati EH, Napolitano C, Priori SG, Schwartz PJ, Towbin JA, Vincent GM, Zhang L.

J Am Coll Cardiol. 2007 Jan 23;49(3):329-37. Epub 2007 Jan 4.

7.

Gender differences in the long QT syndrome: effects of beta-adrenoceptor blockade.

Conrath CE, Wilde AA, Jongbloed RJ, Alders M, van Langen IM, van Tintelen JP, Doevendans PA, Opthof T.

Cardiovasc Res. 2002 Feb 15;53(3):770-6.

PMID:
11861047
8.

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.

Stattin EL, Boström IM, Winbo A, Cederquist K, Jonasson J, Jonsson BA, Diamant UB, Jensen SM, Rydberg A, Norberg A.

BMC Cardiovasc Disord. 2012 Oct 25;12:95. doi: 10.1186/1471-2261-12-95.

9.

Characterization of a KCNQ1/KVLQT1 polymorphism in Asian families with LQT2: implications for genetic testing.

Sharma D, Glatter KA, Timofeyev V, Tuteja D, Zhang Z, Rodriguez J, Tester DJ, Low R, Scheinman MM, Ackerman MJ, Chiamvimonvat N.

J Mol Cell Cardiol. 2004 Jul;37(1):79-89.

PMID:
15242738
10.

Role of alpha1-blockade in congenital long QT syndrome: investigation by exercise stress test.

Furushima H, Chinushi M, Washizuka T, Aizawa Y.

Jpn Circ J. 2001 Jul;65(7):654-8.

11.

Analysis of candidate genes for genotypic diagnosis in the long QT syndrome.

Haack B, Kupka S, Ebauer M, Siemiatkowska A, Pfister M, Kwiatkowska J, Ereciński J, Limon J, Ochman K, Blin N.

J Appl Genet. 2004;45(3):375-81.

PMID:
15306731
12.

Genetic testing of patients with long QT syndrome.

Jiménez-Jáimez J, Tercedor-Sánchez L, Alvarez-López M, Martínez-Espín E, Sebastián Galdeano R, Almansa-Valencia I, Lorente JA, Melgares-Moreno R.

Rev Esp Cardiol. 2011 Jan;64(1):71-4. doi: 10.1016/j.recesp.2010.10.002. Epub 2010 Dec 3.

13.

Clinical management of patients with the long QT syndrome: drugs, devices, and gene-specific therapy.

Moss AJ.

Pacing Clin Electrophysiol. 1997 Aug;20(8 Pt 2):2058-60. Review.

PMID:
9272508
14.

D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.

Nishio Y, Makiyama T, Itoh H, Sakaguchi T, Ohno S, Gong YZ, Yamamoto S, Ozawa T, Ding WG, Toyoda F, Kawamura M, Akao M, Matsuura H, Kimura T, Kita T, Horie M.

J Am Coll Cardiol. 2009 Aug 25;54(9):812-9. doi: 10.1016/j.jacc.2009.06.005.

15.

Malignant familial long QT syndrome.

Subramanyan R, Venugopalan P.

Saudi Med J. 2002 Jun;23(6):738-42.

PMID:
12070560
16.

Beta blockers normalize QT hysteresis in long QT syndrome.

Krahn AD, Yee R, Chauhan V, Skanes AC, Wang J, Hegele RA, Klein GJ.

Am Heart J. 2002 Mar;143(3):528-34.

PMID:
11868061
17.

Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.

Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M.

Hum Mutat. 2009 Apr;30(4):557-63. doi: 10.1002/humu.20834.

PMID:
19306396
18.
19.

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.

Jongbloed R, Marcelis C, Velter C, Doevendans P, Geraedts J, Smeets H.

Hum Mutat. 2002 Nov;20(5):382-91.

PMID:
12402336
20.

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