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Results: 1 to 20 of 96

Similar articles for PubMed (Select 9521325)

1.

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.

Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, Potenza D, Moya A, Borggrefe M, Breithardt G, Ortiz-Lopez R, Wang Z, Antzelevitch C, O'Brien RE, Schulze-Bahr E, Keating MT, Towbin JA, Wang Q.

Nature. 1998 Mar 19;392(6673):293-6.

PMID:
9521325
2.
3.

Accelerated inactivation in a mutant Na(+) channel associated with idiopathic ventricular fibrillation.

Wan X, Chen S, Sadeghpour A, Wang Q, Kirsch GE.

Am J Physiol Heart Circ Physiol. 2001 Jan;280(1):H354-60.

4.

Cardiac Na(+) channel dysfunction in Brugada syndrome is aggravated by beta(1)-subunit.

Makita N, Shirai N, Wang DW, Sasaki K, George AL Jr, Kanno M, Kitabatake A.

Circulation. 2000 Jan 4-11;101(1):54-60.

5.

Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization.

Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Makiyama T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Kimura A, Maemura K, Watanabe I, Kamakura S, Horie M, Aizawa Y, Shimizu W, Makita N.

Circ Arrhythm Electrophysiol. 2011 Dec;4(6):874-81. doi: 10.1161/CIRCEP.111.963983. Epub 2011 Oct 25.

6.

Clinical and electrophysiological characteristics of Brugada syndrome caused by a missense mutation in the S5-pore site of SCN5A.

Itoh H, Shimizu M, Mabuchi H, Imoto K.

J Cardiovasc Electrophysiol. 2005 Apr;16(4):378-83.

PMID:
15828879
7.

Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation.

Valdivia CR, Medeiros-Domingo A, Ye B, Shen WK, Algiers TJ, Ackerman MJ, Makielski JC.

Cardiovasc Res. 2010 Jun 1;86(3):392-400. doi: 10.1093/cvr/cvp417. Epub 2009 Dec 30.

8.

A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.

Akai J, Makita N, Sakurada H, Shirai N, Ueda K, Kitabatake A, Nakazawa K, Kimura A, Hiraoka M.

FEBS Lett. 2000 Aug 11;479(1-2):29-34.

9.

Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.

Schulze-Bahr E, Eckardt L, Breithardt G, Seidl K, Wichter T, Wolpert C, Borggrefe M, Haverkamp W.

Hum Mutat. 2003 Jun;21(6):651-2. Erratum in: Hum Mutat. 2005 Jul;26(1):61.

PMID:
14961552
10.

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

Baroudi G, Pouliot V, Denjoy I, Guicheney P, Shrier A, Chahine M.

Circ Res. 2001 Jun 22;88(12):E78-83.

11.

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA.

Mol Genet Metab. 2002 Apr;75(4):317-24.

PMID:
12051963
12.

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA.

Hum Mol Genet. 2002 Feb 1;11(3):337-45.

13.

Molecular mechanism for an inherited cardiac arrhythmia.

Bennett PB, Yazawa K, Makita N, George AL Jr.

Nature. 1995 Aug 24;376(6542):683-5.

PMID:
7651517
14.

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

Rook MB, Bezzina Alshinawi C, Groenewegen WA, van Gelder IC, van Ginneken AC, Jongsma HJ, Mannens MM, Wilde AA.

Cardiovasc Res. 1999 Dec;44(3):507-17.

15.

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome.

Wang DW, Makita N, Kitabatake A, Balser JR, George AL Jr.

Circ Res. 2000 Oct 13;87(8):E37-43.

16.

A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation.

Keller DI, Huang H, Zhao J, Frank R, Suarez V, Delacrétaz E, Brink M, Osswald S, Schwick N, Chahine M.

Cardiovasc Res. 2006 Jun 1;70(3):521-9. Epub 2006 Mar 3.

17.

Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity.

Levy-Nissenbaum E, Eldar M, Wang Q, Lahat H, Belhassen B, Ries L, Friedman E, Pras E.

Genet Test. 2001 Winter;5(4):331-4.

PMID:
11960580
18.

The LQT syndromes--current status of molecular mechanisms.

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

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
19.

SNP S1103Y in the cardiac sodium channel gene SCN5A is associated with cardiac arrhythmias and sudden death in a white family.

Chen S, Chung MK, Martin D, Rozich R, Tchou PJ, Wang Q.

J Med Genet. 2002 Dec;39(12):913-5.

20.

Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.

Wei J, Wang DW, Alings M, Fish F, Wathen M, Roden DM, George AL Jr.

Circulation. 1999 Jun 22;99(24):3165-71.

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