Wilde AAM - Search Results

1

Prediction of ventricular arrhythmia in phospholamban p.Arg14del mutation carriers-reaching the frontiers of individual risk prediction.

Verstraelen TE, van Lint FHM, Bosman LP, de Brouwer R, Proost VM, Abeln BGS, Taha K, Zwinderman AH, Dickhoff C, Oomen T, Schoonderwoerd BA, Kimman GP, Houweling AC, Gimeno-Blanes JR, Asselbergs FW, van der Zwaag PA, de Boer RA, van den Berg MP, van Tintelen JP, Wilde AAM. Verstraelen TE, et al. Among authors: wilde aam. Eur Heart J. 2021 Jul 31;42(29):2842-2850. doi: 10.1093/eurheartj/ehab294. Eur Heart J. 2021. PMID: 34113975 Free PMC article.

2

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. Conrath CE, et al. Cardiovasc Res. 2002 Feb 15;53(3):770-6. doi: 10.1016/s0008-6363(01)00477-1. Cardiovasc Res. 2002. PMID: 11861047

3

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. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

4

Diagnostic performance of various QTc interval formulas in a large family with long QT syndrome type 3: Bazett's formula not so bad after all..

Brouwer J, Van Den Berg MP, Grobbee DE, Haaksma J, Wilde AA. Brouwer J, et al. Ann Noninvasive Electrocardiol. 2003 Oct;8(4):269-74. doi: 10.1046/j.1542-474x.2003.08402.x. Ann Noninvasive Electrocardiol. 2003. PMID: 14516281 Free PMC article.

5

High distress in parents whose children undergo predictive testing for long QT syndrome.

Hendriks KS, Grosfeld FJ, Wilde AA, van den Bout J, van Langen IM, van Tintelen JP, ten Kroode HF. Hendriks KS, et al. Community Genet. 2005;8(2):103-13. doi: 10.1159/000084778. Community Genet. 2005. PMID: 15925886

6

Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood.

Beaufort-Krol GC, van den Berg MP, Wilde AA, van Tintelen JP, Viersma JW, Bezzina CR, Bink-Boelkens MT. Beaufort-Krol GC, et al. J Am Coll Cardiol. 2005 Jul 19;46(2):331-7. doi: 10.1016/j.jacc.2005.03.066. J Am Coll Cardiol. 2005. PMID: 16022964 Free article.

7

Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome.

Hendriks KS, Grosfeld FJ, van Tintelen JP, van Langen IM, Wilde AA, van den Bout J, ten Kroode HF. Hendriks KS, et al. Am J Med Genet A. 2005 Oct 1;138A(2):107-12. doi: 10.1002/ajmg.a.30861. Am J Med Genet A. 2005. PMID: 16149070

8

Ten years of genes in inherited arrhythmia syndromes: an example of what we have learned from patients, electrocardiograms, and computers.

Wilde AA, van den Berg MP. Wilde AA, et al. J Electrocardiol. 2005 Oct;38(4 Suppl):145-9. doi: 10.1016/j.jelectrocard.2005.06.103. J Electrocardiol. 2005. PMID: 16226090 Review.

9

Diurnal variation of ventricular repolarization in a large family with LQT3-Brugada syndrome characterized by nocturnal sudden death.

van den Berg MP, Haaksma J, Veeger NJ, Wilde AA. van den Berg MP, et al. Heart Rhythm. 2006 Mar;3(3):290-5. doi: 10.1016/j.hrthm.2005.11.023. Heart Rhythm. 2006. PMID: 16500301

10

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.

van Tintelen JP, Entius MM, Bhuiyan ZA, Jongbloed R, Wiesfeld AC, Wilde AA, van der Smagt J, Boven LG, Mannens MM, van Langen IM, Hofstra RM, Otterspoor LC, Doevendans PA, Rodriguez LM, van Gelder IC, Hauer RN. van Tintelen JP, et al. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 Mar 27. Circulation. 2006. PMID: 16567567

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