Kass RS - Search Results

1

Proposed diagnostic criteria for the Brugada syndrome: consensus report.

Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA; Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology. Wilde AA, et al. Among authors: kass rs. Circulation. 2002 Nov 5;106(19):2514-9. doi: 10.1161/01.cir.0000034169.45752.4a. Circulation. 2002. PMID: 12417552 Review. No abstract available.

2

Proposed diagnostic criteria for the Brugada syndrome.

Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA; Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology. Wilde AA, et al. Among authors: kass rs. Eur Heart J. 2002 Nov;23(21):1648-54. doi: 10.1053/euhj.2002.3382. Eur Heart J. 2002. PMID: 12448445 Review. No abstract available.

3

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. Abriel H, et al. Among authors: kass rs. Circ Res. 2001 Apr 13;88(7):740-5. doi: 10.1161/hh0701.089668. Circ Res. 2001. PMID: 11304498

4

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. Benhorin J, et al. Among authors: kass rs. Ann Noninvasive Electrocardiol. 2002 Jan;7(1):40-6. doi: 10.1111/j.1542-474x.2001.tb00137.x. Ann Noninvasive Electrocardiol. 2002. PMID: 11844290 Free PMC article.

5

A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction.

Rivolta I, Clancy CE, Tateyama M, Liu H, Priori SG, Kass RS. Rivolta I, et al. Among authors: kass rs. Physiol Genomics. 2002 Sep 3;10(3):191-7. doi: 10.1152/physiolgenomics.00039.2002. Physiol Genomics. 2002. PMID: 12209021

6

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes.

Rivolta I, Abriel H, Tateyama M, Liu H, Memmi M, Vardas P, Napolitano C, Priori SG, Kass RS. Rivolta I, et al. Among authors: kass rs. J Biol Chem. 2001 Aug 17;276(33):30623-30. doi: 10.1074/jbc.M104471200. Epub 2001 Jun 15. J Biol Chem. 2001. PMID: 11410597 Free article.

7

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. Benhorin J, et al. Among authors: kass rs. Circulation. 2000 Apr 11;101(14):1698-706. doi: 10.1161/01.cir.101.14.1698. Circulation. 2000. PMID: 10758053

8

Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.

Shushi L, Kerem B, Goldmit M, Peretz A, Attali B, Medina A, Towbin JA, Kurokawa J, Kass RS, Benhorin J. Shushi L, et al. Among authors: kass rs. Ann Noninvasive Electrocardiol. 2005 Jul;10(3):334-41. doi: 10.1111/j.1542-474X.2005.00643.x. Ann Noninvasive Electrocardiol. 2005. PMID: 16029385 Free PMC article.

9

Unique cardiac Purkinje fiber transient outward current β-subunit composition: a potential molecular link to idiopathic ventricular fibrillation.

Xiao L, Koopmann TT, Ördög B, Postema PG, Verkerk AO, Iyer V, Sampson KJ, Boink GJ, Mamarbachi MA, Varro A, Jordaens L, Res J, Kass RS, Wilde AA, Bezzina CR, Nattel S. Xiao L, et al. Among authors: kass rs. Circ Res. 2013 May 10;112(10):1310-22. doi: 10.1161/CIRCRESAHA.112.300227. Epub 2013 Mar 26. Circ Res. 2013. PMID: 23532596 Free PMC article.

10

Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome.

Abriel H, Wehrens XH, Benhorin J, Kerem B, Kass RS. Abriel H, et al. Among authors: kass rs. Circulation. 2000 Aug 22;102(8):921-5. doi: 10.1161/01.cir.102.8.921. Circulation. 2000. PMID: 10952963

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