Tanck MWT - Search Results

1

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy.

Rivaud MR, Jansen JA, Postema PG, Nannenberg EA, Mizusawa Y, van der Nagel R, Wolswinkel R, van der Made I, Marchal GA, Rajamani S, Belardinelli L, van Tintelen JP, Tanck MWT, van der Wal AC, de Bakker JMT, van Rijen HV, Creemers EE, Wilde AAM, van den Berg MP, van Veen TAB, Bezzina CR, Remme CA. Rivaud MR, et al. Among authors: tanck mwt. Eur Heart J. 2018 Aug 14;39(31):2898-2907. doi: 10.1093/eurheartj/ehy247. Eur Heart J. 2018. PMID: 29718149

2

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

Bezzina CR, Shimizu W, Yang P, Koopmann TT, Tanck MW, Miyamoto Y, Kamakura S, Roden DM, Wilde AA. Bezzina CR, et al. Circulation. 2006 Jan 24;113(3):338-44. doi: 10.1161/CIRCULATIONAHA.105.580811. Epub 2006 Jan 16. Circulation. 2006. PMID: 16415376

3

Diagnosing familial hypercholesterolaemia: the relevance of genetic testing.

van Aalst-Cohen ES, Jansen AC, Tanck MW, Defesche JC, Trip MD, Lansberg PJ, Stalenhoef AF, Kastelein JJ. van Aalst-Cohen ES, et al. Eur Heart J. 2006 Sep;27(18):2240-6. doi: 10.1093/eurheartj/ehl113. Epub 2006 Jul 6. Eur Heart J. 2006. PMID: 16825289

4

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients.

Dekker LR, Bezzina CR, Henriques JP, Tanck MW, Koch KT, Alings MW, Arnold AE, de Boer MJ, Gorgels AP, Michels HR, Verkerk A, Verheugt FW, Zijlstra F, Wilde AA. Dekker LR, et al. Circulation. 2006 Sep 12;114(11):1140-5. doi: 10.1161/CIRCULATIONAHA.105.606145. Epub 2006 Aug 28. Circulation. 2006. PMID: 16940195

5

Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia.

Souverein OW, Defesche JC, Zwinderman AH, Kastelein JJ, Tanck MW. Souverein OW, et al. Eur Heart J. 2007 Feb;28(3):299-304. doi: 10.1093/eurheartj/ehl366. Epub 2006 Nov 7. Eur Heart J. 2007. PMID: 17090611

6

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

Hofman N, Wilde AA, Kääb S, van Langen IM, Tanck MW, Mannens MM, Hinterseer M, Beckmann BM, Tan HL. Hofman N, et al. Eur Heart J. 2007 Mar;28(5):575-80. doi: 10.1093/eurheartj/ehl355. Epub 2006 Nov 7. Eur Heart J. 2007. PMID: 17090615

7

A novel echocardiographic predictor of in-hospital mortality and mid-term haemodynamic improvement after pulmonary endarterectomy for chronic thrombo-embolic pulmonary hypertension.

Hardziyenka M, Reesink HJ, Bouma BJ, de Bruin-Bon HA, Campian ME, Tanck MW, van den Brink RB, Kloek JJ, Tan HL, Bresser P. Hardziyenka M, et al. Eur Heart J. 2007 Apr;28(7):842-9. doi: 10.1093/eurheartj/ehl534. Epub 2007 Mar 6. Eur Heart J. 2007. PMID: 17341501

8

Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.

Meregalli PG, Tan HL, Probst V, Koopmann TT, Tanck MW, Bhuiyan ZA, Sacher F, Kyndt F, Schott JJ, Albuisson J, Mabo P, Bezzina CR, Le Marec H, Wilde AA. Meregalli PG, et al. Heart Rhythm. 2009 Mar;6(3):341-8. doi: 10.1016/j.hrthm.2008.11.009. Epub 2008 Nov 11. Heart Rhythm. 2009. PMID: 19251209

9

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.

Alders M, Koopmann TT, Christiaans I, Postema PG, Beekman L, Tanck MW, Zeppenfeld K, Loh P, Koch KT, Demolombe S, Mannens MM, Bezzina CR, Wilde AA. Alders M, et al. Am J Hum Genet. 2009 Apr;84(4):468-76. doi: 10.1016/j.ajhg.2009.02.009. Epub 2009 Mar 12. Am J Hum Genet. 2009. PMID: 19285295 Free PMC article.

10

Prognosis among survivors of primary ventricular fibrillation in the percutaneous coronary intervention era.

de Jong JS, Marsman RF, Henriques JP, Koch KT, de Winter RJ, Tanck MW, Wilde AA, Dekker LR. de Jong JS, et al. Am Heart J. 2009 Sep;158(3):467-72. doi: 10.1016/j.ahj.2009.06.028. Am Heart J. 2009. PMID: 19699872 Free article.

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