Wilde AA - Search Results

1

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.

Kannankeril PJ, Bhuiyan ZA, Darbar D, Mannens MM, Wilde AA, Roden DM. Kannankeril PJ, et al. Among authors: wilde aa. Heart Rhythm. 2006 Aug;3(8):939-44. doi: 10.1016/j.hrthm.2006.04.028. Epub 2006 May 3. Heart Rhythm. 2006. PMID: 16876743

2

KVLQT1, the rhythm of imprinting.

Mannens M, Wilde A. Mannens M, et al. Nat Genet. 1997 Feb;15(2):113-5. doi: 10.1038/ng0297-113. Nat Genet. 1997. PMID: 9020829 No abstract available.

3

A calcium sensor in the sodium channel modulates cardiac excitability.

Tan HL, Kupershmidt S, Zhang R, Stepanovic S, Roden DM, Wilde AA, Anderson ME, Balser JR. Tan HL, et al. Among authors: wilde aa. Nature. 2002 Jan 24;415(6870):442-7. doi: 10.1038/415442a. Nature. 2002. PMID: 11807557

4

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia.

Postma AV, Denjoy I, Hoorntje TM, Lupoglazoff JM, Da Costa A, Sebillon P, Mannens MM, Wilde AA, Guicheney P. Postma AV, et al. Among authors: wilde aa. Circ Res. 2002 Oct 18;91(8):e21-6. doi: 10.1161/01.res.0000038886.18992.6b. Circ Res. 2002. PMID: 12386154

5

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AA, Mannens MM. Bezzina CR, et al. Among authors: wilde aa. Circ Res. 2003 Feb 7;92(2):159-68. doi: 10.1161/01.res.0000052672.97759.36. Circ Res. 2003. PMID: 12574143

6

A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.

Groenewegen WA, Bezzina CR, van Tintelen JP, Hoorntje TM, Mannens MM, Wilde AA, Jongsma HJ, Rook MB. Groenewegen WA, et al. Among authors: wilde aa. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

7

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.

Bezzina CR, Verkerk AO, Busjahn A, Jeron A, Erdmann J, Koopmann TT, Bhuiyan ZA, Wilders R, Mannens MM, Tan HL, Luft FC, Schunkert H, Wilde AA. Bezzina CR, et al. Among authors: wilde aa. Cardiovasc Res. 2003 Jul 1;59(1):27-36. doi: 10.1016/s0008-6363(03)00342-0. Cardiovasc Res. 2003. PMID: 12829173

8

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.

Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, Baró I, Wilde AA. Bellocq C, et al. Among authors: wilde aa. Circulation. 2004 May 25;109(20):2394-7. doi: 10.1161/01.CIR.0000130409.72142.FE. Circulation. 2004. PMID: 15159330

9

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA. Smits JP, et al. Among authors: wilde aa. J Mol Cell Cardiol. 2005 Jun;38(6):969-81. doi: 10.1016/j.yjmcc.2005.02.024. Epub 2005 Apr 1. J Mol Cell Cardiol. 2005. PMID: 15910881

10

The molecular genetics of arrhythmias.

Bezzina CR, Wilde AA, Roden DM. Bezzina CR, et al. Among authors: wilde aa. Cardiovasc Res. 2005 Aug 15;67(3):343-6. doi: 10.1016/j.cardiores.2005.06.004. Cardiovasc Res. 2005. PMID: 16005449 No abstract available.

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