van Tintelen JP - Search Results

1

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.

van Tintelen JP, Entius MM, Bhuiyan ZA, Jongbloed R, Wiesfeld AC, Wilde AA, van der Smagt J, Boven LG, Mannens MM, van Langen IM, Hofstra RM, Otterspoor LC, Doevendans PA, Rodriguez LM, van Gelder IC, Hauer RN. van Tintelen JP, et al. Among authors: van der smagt j, van langen im, van gelder ic. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 Mar 27. Circulation. 2006. PMID: 16567567

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

[Long QT-interval syndrome and investigation of heritability: psychological reactions in three generations in one family].

ten Kroode HF, van Langen IM, Hendriks KS, van Tintelen JP, Grosfeld FJ, Wilde AA. ten Kroode HF, et al. Among authors: van langen im, van tintelen jp. Ned Tijdschr Geneeskd. 2000 May 20;144(21):995-9. Ned Tijdschr Geneeskd. 2000. PMID: 10858789 Dutch.

6

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

7

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

8

[Arrhythmogenic right-ventricular cardiomyopathy: different manifestations as precursors of sudden death which might be prevented].

van der Harst P, Wiesfeld AC, van Gelder IC, van Tintelen JP, Suurmeijer AJ, van Veldhuisen DJ. van der Harst P, et al. Among authors: van gelder ic, van tintelen jp, van veldhuisen dj. Ned Tijdschr Geneeskd. 2004 Nov 27;148(48):2396-402. Ned Tijdschr Geneeskd. 2004. PMID: 15615276 Dutch.

9

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.

10

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

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