van Tintelen JP - 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: van rijen hv, van veen tab, van der made i, van den berg mp, van der nagel r, van tintelen jp, van der wal ac. Eur Heart J. 2018 Aug 14;39(31):2898-2907. doi: 10.1093/eurheartj/ehy247. Eur Heart J. 2018. PMID: 29718149

2

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

Wilde AA, Jongbloed RJ, Doevendans PA, Düren DR, Hauer RN, van Langen IM, van Tintelen JP, Smeets HJ, Meyer H, Geelen JL. Wilde AA, et al. Among authors: van langen im, van tintelen jp. J Am Coll Cardiol. 1999 Feb;33(2):327-32. doi: 10.1016/s0735-1097(98)00578-6. J Am Coll Cardiol. 1999. PMID: 9973011 Free article.

3

[Presymptomatic screening after a sudden cardiac death in the family].

Wilde AA, van Langen IM, van Tintelen JP, Hauer RN. Wilde AA, et al. Among authors: van langen im, van tintelen jp. Ned Tijdschr Geneeskd. 1999 Aug 7;143(32):1643-8. Ned Tijdschr Geneeskd. 1999. PMID: 10494298 Review. Dutch.

4

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: van langen im, van tintelen jp. Cardiovasc Res. 2002 Feb 15;53(3):770-6. doi: 10.1016/s0008-6363(01)00477-1. Cardiovasc Res. 2002. PMID: 11861047

5

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: van tintelen jp. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

6

[Implantable cardioverter-defibrillator in the treatment of two patients with an increased risk of sudden cardiac death].

van den Berg MP, van Tintelen JP, van Dessel PF, van Veldhuisen DJ. van den Berg MP, et al. Among authors: van dessel pf, van tintelen jp, van veldhuisen dj. Ned Tijdschr Geneeskd. 2004 Oct 23;148(43):2132-5. Ned Tijdschr Geneeskd. 2004. PMID: 15553359 Dutch.

7

Genetic aspects of atrial fibrillation.

Wiesfeld AC, Hemels ME, Van Tintelen JP, Van den Berg MP, Van Veldhuisen DJ, Van Gelder IC. Wiesfeld AC, et al. Among authors: van den berg mp, van gelder ic, van tintelen jp, van veldhuisen dj. Cardiovasc Res. 2005 Aug 15;67(3):414-8. doi: 10.1016/j.cardiores.2005.04.033. Cardiovasc Res. 2005. PMID: 15921669 Review.

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: van den bout j, van langen im, van tintelen jp. Community Genet. 2005;8(2):103-13. doi: 10.1159/000084778. Community Genet. 2005. PMID: 15925886

9

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: van den berg mp, van tintelen jp. 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.

10

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: van den bout j, van langen im, van tintelen jp. 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

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