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149 results

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Page 1
Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia.
Lieve KVV, Verhagen JMA, Wei J, Bos JM, van der Werf C, Rosés I Noguer F, Mancini GMS, Guo W, Wang R, van den Heuvel F, Frohn-Mulder IME, Shimizu W, Nogami A, Horigome H, Roberts JD, Leenhardt A, Crijns HJG, Blank AC, Aiba T, Wiesfeld ACP, Blom NA, Sumitomo N, Till J, Ackerman MJ, Chen SRW, van de Laar IMBH, Wilde AAM. Lieve KVV, et al. Among authors: van den heuvel f, van de laar imbh, van der werf c. Heart Rhythm. 2019 Feb;16(2):220-228. doi: 10.1016/j.hrthm.2018.08.025. Epub 2018 Aug 28. Heart Rhythm. 2019. PMID: 30170228
Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives.
van der Werf C, Nederend I, Hofman N, van Geloven N, Ebink C, Frohn-Mulder IM, Alings AM, Bosker HA, Bracke FA, van den Heuvel F, Waalewijn RA, Bikker H, van Tintelen JP, Bhuiyan ZA, van den Berg MP, Wilde AA. van der Werf C, et al. Among authors: van den heuvel f, van den berg mp, van tintelen jp, van geloven n. Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):748-56. doi: 10.1161/CIRCEP.112.970517. Epub 2012 Jul 10. Circ Arrhythm Electrophysiol. 2012. PMID: 22787013
A family with Andersen-Tawil syndrome and dilated cardiomyopathy.
Schoonderwoerd BA, Wiesfeld AC, Wilde AA, van den Heuvel F, Van Tintelen JP, van den Berg MP, Van Veldhuisen DJ, Van Gelder IC. Schoonderwoerd BA, et al. Among authors: van den heuvel f, van den berg mp, van gelder ic, van tintelen jp, van veldhuisen dj. Heart Rhythm. 2006 Nov;3(11):1346-50. doi: 10.1016/j.hrthm.2006.07.021. Epub 2006 Jul 21. Heart Rhythm. 2006. PMID: 17074642 No abstract available.
Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene.
van Tintelen JP, Van Gelder IC, Asimaki A, Suurmeijer AJ, Wiesfeld AC, Jongbloed JD, van den Wijngaard A, Kuks JB, van Spaendonck-Zwarts KY, Notermans N, Boven L, van den Heuvel F, Veenstra-Knol HE, Saffitz JE, Hofstra RM, van den Berg MP. van Tintelen JP, et al. Among authors: van spaendonck zwarts ky, van den heuvel f, van den berg mp, van gelder ic, van den wijngaard a. Heart Rhythm. 2009 Nov;6(11):1574-83. doi: 10.1016/j.hrthm.2009.07.041. Epub 2009 Jul 28. Heart Rhythm. 2009. PMID: 19879535
Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: higher recurrence of events under metoprolol.
Chockalingam P, Crotti L, Girardengo G, Johnson JN, Harris KM, van der Heijden JF, Hauer RN, Beckmann BM, Spazzolini C, Rordorf R, Rydberg A, Clur SA, Fischer M, van den Heuvel F, Kääb S, Blom NA, Ackerman MJ, Schwartz PJ, Wilde AA. Chockalingam P, et al. Among authors: van der heijden jf, van den heuvel f. J Am Coll Cardiol. 2012 Nov 13;60(20):2092-9. doi: 10.1016/j.jacc.2012.07.046. Epub 2012 Oct 17. J Am Coll Cardiol. 2012. PMID: 23083782 Free PMC article.
Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy.
Roudijk RW, Verheul L, Bosman LP, Bourfiss M, Breur JMPJ, Slieker MG, Blank AC, Dooijes D, van der Heijden JF, van den Heuvel F, Clur SA, Udink Ten Cate FEA, van den Berg MP, Wilde AAM, Asselbergs FW, Peter van Tintelen J, Te Riele ASJM. Roudijk RW, et al. Among authors: van der heijden jf, van den heuvel f, van den berg mp. JACC Clin Electrophysiol. 2022 Mar;8(3):306-318. doi: 10.1016/j.jacep.2021.09.001. Epub 2021 Dec 22. JACC Clin Electrophysiol. 2022. PMID: 35331425 Free article.
KinCor, a national registry for paediatric patients with congenital and other types of heart disease in the Netherlands: aims, design and interim results.
Silva LM, Kuipers IM, van den Heuvel F, Mendes R, Berger RM, van Beynum IM, Rozendaal L, Rammeloo LA, van Iperen GG, Schokking M, Frerich S, Blom NA, Breur JM, Helbing WA. Silva LM, et al. Among authors: van den heuvel f, van iperen gg, van beynum im. Neth Heart J. 2016 Nov;24(11):628-639. doi: 10.1007/s12471-016-0892-9. Neth Heart J. 2016. PMID: 27632192 Free PMC article.
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.
149 results