Van Tintelen JP - Search Results

1

Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide.

Postema PG, Van den Berg M, Van Tintelen JP, Van den Heuvel F, Grundeken M, Hofman N, Van der Roest WP, Nannenberg EA, Krapels IP, Bezzina CR, Wilde A. Postema PG, et al. Among authors: van den berg m, van den heuvel f, van der roest wp, van tintelen jp. Neth Heart J. 2009 Nov;17(11):422-8. doi: 10.1007/BF03086296. Neth Heart J. 2009. PMID: 19949711 Free PMC article.

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

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.

Jongbloed RJ, Wilde AA, Geelen JL, Doevendans P, Schaap C, Van Langen I, van Tintelen JP, Cobben JM, Beaufort-Krol GC, Geraedts JP, Smeets HJ. Jongbloed RJ, et al. Among authors: van langen i, van tintelen jp. Hum Mutat. 1999;13(4):301-10. doi: 10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V. Hum Mutat. 1999. PMID: 10220144

4

[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.

5

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

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: 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

7

[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.

8

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.

9

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

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: 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.

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