Wilde AAM - Search Results

1

Sex-specific aspects of phospholamban cardiomyopathy: The importance and prognostic value of low-voltage electrocardiograms.

de Brouwer R, Meems LMG, Verstraelen TE, Mahmoud B, Proost V, Wilde AAM, Bosman LP, van Drie E, van der Zwaag PA, van Tintelen JP, Houweling AC, van den Berg MP, de Boer RA. de Brouwer R, et al. Among authors: wilde aam. Heart Rhythm. 2022 Mar;19(3):427-434. doi: 10.1016/j.hrthm.2021.11.009. Epub 2021 Nov 9. Heart Rhythm. 2022. PMID: 34767988 Free 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

Is there a genetic basis for malignant ventricular arrhythmias?

Wilde AA, Dekker LR. Wilde AA, et al. Heart Rhythm. 2005 Oct;2(10):1145-7. doi: 10.1016/j.hrthm.2005.06.017. Heart Rhythm. 2005. PMID: 16188598 Review. No abstract available.

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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