Wilde AA - Search Results

1

T-cell-mediated inflammatory activity in the stellate ganglia of patients with ion-channel disease and severe ventricular arrhythmias.

Rizzo S, Basso C, Troost D, Aronica E, Frigo AC, Driessen AH, Thiene G, Wilde AA, van der Wal AC. Rizzo S, et al. Among authors: wilde aa. Circ Arrhythm Electrophysiol. 2014 Apr;7(2):224-9. doi: 10.1161/CIRCEP.113.001184. Epub 2014 Feb 14. Circ Arrhythm Electrophysiol. 2014. PMID: 24532560

2

Homozygous premature truncation of the HERG protein : the human HERG knockout.

Hoorntje T, Alders M, van Tintelen P, van der Lip K, Sreeram N, van der Wal A, Mannens M, Wilde A. Hoorntje T, et al. Circulation. 1999 Sep 21;100(12):1264-7. doi: 10.1161/01.cir.100.12.1264. Circulation. 1999. PMID: 10491368

3

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

4

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

Tan HL, Hofman N, van Langen IM, van der Wal AC, Wilde AA. Tan HL, et al. Among authors: wilde aa. Circulation. 2005 Jul 12;112(2):207-13. doi: 10.1161/CIRCULATIONAHA.104.522581. Epub 2005 Jul 5. Circulation. 2005. PMID: 15998675

5

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

Coronel R, Casini S, Koopmann TT, Wilms-Schopman FJ, Verkerk AO, de Groot JR, Bhuiyan Z, Bezzina CR, Veldkamp MW, Linnenbank AC, van der Wal AC, Tan HL, Brugada P, Wilde AA, de Bakker JM. Coronel R, et al. Among authors: wilde aa. Circulation. 2005 Nov 1;112(18):2769-77. doi: 10.1161/CIRCULATIONAHA.105.532614. Circulation. 2005. PMID: 16267250

6

The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

Crotti L, Spazzolini C, Schwartz PJ, Shimizu W, Denjoy I, Schulze-Bahr E, Zaklyazminskaya EV, Swan H, Ackerman MJ, Moss AJ, Wilde AA, Horie M, Brink PA, Insolia R, De Ferrari GM, Crimi G. Crotti L, et al. Among authors: wilde aa. Circulation. 2007 Nov 20;116(21):2366-75. doi: 10.1161/CIRCULATIONAHA.107.726950. Epub 2007 Nov 5. Circulation. 2007. PMID: 17984373

7

Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy.

Pilichou K, Remme CA, Basso C, Campian ME, Rizzo S, Barnett P, Scicluna BP, Bauce B, van den Hoff MJ, de Bakker JM, Tan HL, Valente M, Nava A, Wilde AA, Moorman AF, Thiene G, Bezzina CR. Pilichou K, et al. Among authors: wilde aa. J Exp Med. 2009 Aug 3;206(8):1787-802. doi: 10.1084/jem.20090641. Epub 2009 Jul 27. J Exp Med. 2009. PMID: 19635863 Free PMC article.

8

Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac development.

Tan HL, van der Wal AC, Campian ME, Kruyswijk HH, ten Hove Jansen B, van Doorn DJ, Oskam HJ, Becker AE, Wilde AA. Tan HL, et al. Among authors: wilde aa. Circ Arrhythm Electrophysiol. 2008 Oct;1(4):276-81. doi: 10.1161/CIRCEP.108.782862. Epub 2008 Sep 12. Circ Arrhythm Electrophysiol. 2008. PMID: 19808419

9

Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands.

van der Werf C, Hofman N, Tan HL, van Dessel PF, Alders M, van der Wal AC, van Langen IM, Wilde AA. van der Werf C, et al. Among authors: wilde aa. Heart Rhythm. 2010 Oct;7(10):1383-9. doi: 10.1016/j.hrthm.2010.05.036. Epub 2010 May 31. Heart Rhythm. 2010. PMID: 20646679

10

A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death.

Marsman RF, Bardai A, Postma AV, Res JC, Koopmann TT, Beekman L, van der Wal AC, Pinto YM, Lekanne Deprez RH, Wilde AA, Jordaens LJ, Bezzina CR. Marsman RF, et al. Among authors: wilde aa. Circ Cardiovasc Genet. 2011 Jun;4(3):280-7. doi: 10.1161/CIRCGENETICS.110.959221. Epub 2011 Mar 15. Circ Cardiovasc Genet. 2011. PMID: 21406687

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