Wilde AA - Search Results

1

Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers.

Christiaans I, van Engelen K, van Langen IM, Birnie E, Bonsel GJ, Elliott PM, Wilde AA. Christiaans I, et al. Among authors: wilde aa. Europace. 2010 Mar;12(3):313-21. doi: 10.1093/europace/eup431. Epub 2010 Jan 29. Europace. 2010. PMID: 20118111 Review.

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. Among authors: wilde aa. Cardiovasc Res. 2002 Feb 15;53(3):770-6. doi: 10.1016/s0008-6363(01)00477-1. Cardiovasc Res. 2002. PMID: 11861047

3

[Hypertrophic cardiomyopathy: a genetically-carried heart disease].

van Dockum WG, Doevendans PA, van Rossum AC, Wilde AA. van Dockum WG, et al. Among authors: wilde aa. Ned Tijdschr Geneeskd. 2002 Apr 13;146(15):705-12. Ned Tijdschr Geneeskd. 2002. PMID: 11980370 Review. Dutch.

4

Reversed remodelling of dilated left sided cardiomyopathy after upgrading from VVIR to VVIR biventricular pacing.

Erol-Yilmaz A, Tukkie R, Schrama TA, Romkes HJ, Wilde AA. Erol-Yilmaz A, et al. Among authors: wilde aa. Europace. 2002 Oct;4(4):445-9. doi: 10.1053/eupc.2002.0252. Europace. 2002. PMID: 12408266

5

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Among authors: wilde aa. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

6

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.

Van Langen IM, Birnie E, Alders M, Jongbloed RJ, Le Marec H, Wilde AA. Van Langen IM, et al. Among authors: wilde aa. J Med Genet. 2003 Feb;40(2):141-5. doi: 10.1136/jmg.40.2.141. J Med Genet. 2003. PMID: 12566525 Free PMC article. No abstract available.

7

Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?

van Langen IM, Birnie E, Leschot NJ, Bonsel GJ, Wilde AA. van Langen IM, et al. Among authors: wilde aa. Eur Heart J. 2003 Mar;24(6):560-6. doi: 10.1016/s0195-668x(02)00522-5. Eur Heart J. 2003. PMID: 12643889

8

The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands.

Alders M, Jongbloed R, Deelen W, van den Wijngaard A, Doevendans P, Ten Cate F, Regitz-Zagrosek V, Vosberg HP, van Langen I, Wilde A, Dooijes D, Mannens M. Alders M, et al. Eur Heart J. 2003 Oct;24(20):1848-53. doi: 10.1016/s0195-668x(03)00466-4. Eur Heart J. 2003. PMID: 14563344

9

Family and population strategies for screening and counselling of inherited cardiac arrhythmias.

van Langen IM, Hofman N, Tan HL, Wilde AA. van Langen IM, et al. Among authors: wilde aa. Ann Med. 2004;36 Suppl 1:116-24. doi: 10.1080/17431380410032526. Ann Med. 2004. PMID: 15176433 Free article.

10

Mechanisms of inherited cardiac conduction disease.

Smits JP, Veldkamp MW, Wilde AA. Smits JP, et al. Among authors: wilde aa. Europace. 2005 Mar;7(2):122-37. doi: 10.1016/j.eupc.2004.11.004. Europace. 2005. PMID: 15763526 Review.

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