Wilde AA - Search Results

1

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. Among authors: wilde aa. 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

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

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

4

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.

5

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

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

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.

8

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. Among authors: wilde aa. Community Genet. 2005;8(2):103-13. doi: 10.1159/000084778. Community Genet. 2005. PMID: 15925886

9

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

10

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. Among authors: wilde aa. 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.

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