Alders M - Search Results

1

Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.

van Spaendonck-Zwarts KY, Posafalvi A, van den Berg MP, Hilfiker-Kleiner D, Bollen IA, Sliwa K, Alders M, Almomani R, van Langen IM, van der Meer P, Sinke RJ, van der Velden J, Van Veldhuisen DJ, van Tintelen JP, Jongbloed JD. van Spaendonck-Zwarts KY, et al. Among authors: alders m. Eur Heart J. 2014 Aug 21;35(32):2165-73. doi: 10.1093/eurheartj/ehu050. Epub 2014 Feb 20. Eur Heart J. 2014. PMID: 24558114

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

3

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

4

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.

Bhuiyan ZA, van den Berg MP, van Tintelen JP, Bink-Boelkens MT, Wiesfeld AC, Alders M, Postma AV, van Langen I, Mannens MM, Wilde AA. Bhuiyan ZA, et al. Among authors: alders m. Circulation. 2007 Oct 2;116(14):1569-76. doi: 10.1161/CIRCULATIONAHA.107.711606. Epub 2007 Sep 17. Circulation. 2007. PMID: 17875969

5

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

Hofman N, Tan HL, Alders M, van Langen IM, Wilde AA. Hofman N, et al. Among authors: alders m. J Am Coll Cardiol. 2010 Jun 8;55(23):2570-6. doi: 10.1016/j.jacc.2009.12.063. J Am Coll Cardiol. 2010. PMID: 20513597 Free article.

6

Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands.

van der Werf C, Hofman N, Tan HL, van Dessel PF, Alders M, van der Wal AC, van Langen IM, Wilde AA. van der Werf C, et al. Among authors: alders m. Heart Rhythm. 2010 Oct;7(10):1383-9. doi: 10.1016/j.hrthm.2010.05.036. Epub 2010 May 31. Heart Rhythm. 2010. PMID: 20646679

7

Mortality of inherited arrhythmia syndromes: insight into their natural history.

Nannenberg EA, Sijbrands EJ, Dijksman LM, Alders M, van Tintelen JP, Birnie M, van Langen IM, Wilde AA. Nannenberg EA, et al. Among authors: alders m. Circ Cardiovasc Genet. 2012 Apr 1;5(2):183-9. doi: 10.1161/CIRCGENETICS.111.961102. Epub 2012 Feb 28. Circ Cardiovasc Genet. 2012. PMID: 22373669

8

Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience.

Hofman N, Tan HL, Alders M, Kolder I, de Haij S, Mannens MM, Lombardi MP, Dit Deprez RH, van Langen I, Wilde AA. Hofman N, et al. Among authors: alders m. Circulation. 2013 Oct 1;128(14):1513-21. doi: 10.1161/CIRCULATIONAHA.112.000091. Epub 2013 Aug 20. Circulation. 2013. PMID: 23963746

9

Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up.

van der Werf C, Stiekema L, Tan HL, Hofman N, Alders M, van der Wal AC, van Langen IM, Wilde AA. van der Werf C, et al. Among authors: alders m. Heart Rhythm. 2014 Oct;11(10):1728-32. doi: 10.1016/j.hrthm.2014.05.028. Epub 2014 May 29. Heart Rhythm. 2014. PMID: 24882506

10

Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant.

Rumping L, Wessels MW, Postma AV, van Schuppen J, van Slegtenhorst MA, Saris JJ, van Tintelen JP, Robertson SP, Alders M, Maas SM, Deprez RHL. Rumping L, et al. Among authors: alders m. Am J Med Genet A. 2021 Dec;185(12):3814-3820. doi: 10.1002/ajmg.a.62417. Epub 2021 Jul 13. Am J Med Genet A. 2021. PMID: 34254723 Free PMC article.

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