Wilde AA - Search Results

1

[Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age].

Akkerhuis JM, Baars HF, Marcelis CL, Akkerhuis KM, Wilde AA. Akkerhuis JM, et al. Among authors: wilde aa. Ned Tijdschr Geneeskd. 2007 Oct 27;151(43):2357-64. Ned Tijdschr Geneeskd. 2007. PMID: 18019210 Dutch.

2

[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.

3

[Sudden death at young age and the importance of molecular-pathologic investigation].

Wilde AA, van Langen IM, Mannens MM, Waalewijn RA, Maes A. Wilde AA, et al. Ned Tijdschr Geneeskd. 2005 Jul 16;149(29):1601-4. Ned Tijdschr Geneeskd. 2005. PMID: 16078763 Dutch.

4

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

5

[Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years].

Hofman N, Postema PG, van Langen IM, Nannenberg EA, Alders M, Jongbloed R, Smeets HJ, Wilde AA. Hofman N, et al. Among authors: wilde aa. Ned Tijdschr Geneeskd. 2007 Mar 17;151(11):644-8. Ned Tijdschr Geneeskd. 2007. PMID: 17441570 Dutch.

6

Not just any ICD device in patients with long-QT syndrome.

Udo EO, Baars HF, Winter JB, Wilde AA. Udo EO, et al. Among authors: wilde aa. Neth Heart J. 2007 Dec;15(12):418-21. doi: 10.1007/BF03086043. Neth Heart J. 2007. PMID: 18239739 Free PMC article.

7

Do patients with long QT syndrome remain at risk for sudden cardiac death after 40 years of age?

Postema PG, Wilde AA. Postema PG, et al. Among authors: wilde aa. Nat Clin Pract Cardiovasc Med. 2008 Oct;5(10):602-3. doi: 10.1038/ncpcardio1305. Epub 2008 Jul 29. Nat Clin Pract Cardiovasc Med. 2008. PMID: 18665134

8

Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.

Christiaans I, Birnie E, Bonsel GJ, Mannens MM, Michels M, Majoor-Krakauer D, Dooijes D, van Tintelen JP, van den Berg MP, Volders PG, Arens YH, van den Wijngaard A, Atsma DE, Helderman-van den Enden AT, Houweling AC, de Boer K, van der Smagt JJ, Hauer RN, Marcelis CL, Timmermans J, van Langen IM, Wilde AA. Christiaans I, et al. Among authors: wilde aa. Eur Heart J. 2011 May;32(9):1161-70. doi: 10.1093/eurheartj/ehr092. Epub 2011 Apr 1. Eur Heart J. 2011. PMID: 21459882

9

[Premature sudden death--consider serious familial heart rhythm disturbances].

Postema PG, Christiaans I, Alders M, Hofman N, Wilde AA. Postema PG, et al. Among authors: wilde aa. Ned Tijdschr Geneeskd. 2011;155(39):A3391. Ned Tijdschr Geneeskd. 2011. PMID: 21961687 Dutch.

10

[Catecholaminergic polymorphic ventricular tachycardia; possible diagnosis in cases of syncope and sudden death of family members].

Lieve KV, Wilde AA, van der Werf C. Lieve KV, et al. Among authors: wilde aa. Ned Tijdschr Geneeskd. 2015;159:A8205. Ned Tijdschr Geneeskd. 2015. PMID: 25650029 Dutch.

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