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Sex differences in hypertrophic cardiomyopathy: new insights.
van Driel B, Nijenkamp L, Huurman R, Michels M, van der Velden J. van Driel B, et al. Among authors: van der velden j. Curr Opin Cardiol. 2019 May;34(3):254-259. doi: 10.1097/HCO.0000000000000612. Curr Opin Cardiol. 2019. PMID: 30747730 Review.
Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction.
van Dijk SJ, Dooijes D, dos Remedios C, Michels M, Lamers JM, Winegrad S, Schlossarek S, Carrier L, ten Cate FJ, Stienen GJ, van der Velden J. van Dijk SJ, et al. Among authors: van der velden j. Circulation. 2009 Mar 24;119(11):1473-83. doi: 10.1161/CIRCULATIONAHA.108.838672. Epub 2009 Mar 9. Circulation. 2009. PMID: 19273718
How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonance.
Germans T, Rüssel IK, Götte MJ, Spreeuwenberg MD, Doevendans PA, Pinto YM, van der Geest RJ, van der Velden J, Wilde AA, van Rossum AC. Germans T, et al. Among authors: van rossum ac, van der geest rj, van der velden j. J Cardiovasc Magn Reson. 2010 Mar 15;12(1):13. doi: 10.1186/1532-429X-12-13. J Cardiovasc Magn Reson. 2010. PMID: 20230637 Free PMC article.
The development of familial hypertrophic cardiomyopathy: from mutation to bedside.
Brouwer WP, van Dijk SJ, Stienen GJ, van Rossum AC, van der Velden J, Germans T. Brouwer WP, et al. Among authors: van rossum ac, van dijk sj, van der velden j. Eur J Clin Invest. 2011 May;41(5):568-78. doi: 10.1111/j.1365-2362.2010.02439.x. Epub 2010 Dec 15. Eur J Clin Invest. 2011. PMID: 21158848 Review.
Carriers of the hypertrophic cardiomyopathy MYBPC3 mutation are characterized by reduced myocardial efficiency in the absence of hypertrophy and microvascular dysfunction.
Timmer SA, Germans T, Brouwer WP, Lubberink M, van der Velden J, Wilde AA, Christiaans I, Lammertsma AA, Knaapen P, van Rossum AC. Timmer SA, et al. Among authors: van rossum ac, van der velden j. Eur J Heart Fail. 2011 Dec;13(12):1283-9. doi: 10.1093/eurjhf/hfr135. Epub 2011 Oct 21. Eur J Heart Fail. 2011. PMID: 22021246 Free article.
Contractile dysfunction irrespective of the mutant protein in human hypertrophic cardiomyopathy with normal systolic function.
van Dijk SJ, Paalberends ER, Najafi A, Michels M, Sadayappan S, Carrier L, Boontje NM, Kuster DW, van Slegtenhorst M, Dooijes D, dos Remedios C, ten Cate FJ, Stienen GJ, van der Velden J. van Dijk SJ, et al. Among authors: van slegtenhorst m, van der velden j. Circ Heart Fail. 2012 Jan;5(1):36-46. doi: 10.1161/CIRCHEARTFAILURE.111.963702. Epub 2011 Dec 16. Circ Heart Fail. 2012. PMID: 22178992 Free article.
Perturbed length-dependent activation in human hypertrophic cardiomyopathy with missense sarcomeric gene mutations.
Sequeira V, Wijnker PJ, Nijenkamp LL, Kuster DW, Najafi A, Witjas-Paalberends ER, Regan JA, Boontje N, Ten Cate FJ, Germans T, Carrier L, Sadayappan S, van Slegtenhorst MA, Zaremba R, Foster DB, Murphy AM, Poggesi C, Dos Remedios C, Stienen GJ, Ho CY, Michels M, van der Velden J. Sequeira V, et al. Among authors: van slegtenhorst ma, van der velden j. Circ Res. 2013 May 24;112(11):1491-505. doi: 10.1161/CIRCRESAHA.111.300436. Epub 2013 Mar 18. Circ Res. 2013. PMID: 23508784 Free PMC article.
Mutations in MYH7 reduce the force generating capacity of sarcomeres in human familial hypertrophic cardiomyopathy.
Witjas-Paalberends ER, Piroddi N, Stam K, van Dijk SJ, Oliviera VS, Ferrara C, Scellini B, Hazebroek M, ten Cate FJ, van Slegtenhorst M, dos Remedios C, Niessen HW, Tesi C, Stienen GJ, Heymans S, Michels M, Poggesi C, van der Velden J. Witjas-Paalberends ER, et al. Among authors: van dijk sj, van slegtenhorst m, van der velden j. Cardiovasc Res. 2013 Aug 1;99(3):432-41. doi: 10.1093/cvr/cvt119. Epub 2013 May 13. Cardiovasc Res. 2013. PMID: 23674513
626 results