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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
Familial occurrence of isolated non-compaction cardiomyopathy.
Lorsheyd A, Cramer MJ, Velthuis BK, Vonken EJ, van der Smagt J, van Tintelen P, Hauer RN. Lorsheyd A, et al. Among authors: van der smagt j, van tintelen p. Eur J Heart Fail. 2006 Dec;8(8):826-31. doi: 10.1016/j.ejheart.2006.02.014. Epub 2006 May 19. Eur J Heart Fail. 2006. PMID: 16713736 Free article.
Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteria.
Cox MG, Nelen MR, Wilde AA, Wiesfeld AC, van der Smagt JJ, Loh P, Cramer MJ, Doevendans PA, van Tintelen JP, de Bakker JM, Hauer RN. Cox MG, et al. Among authors: van der smagt jj, van tintelen jp. J Cardiovasc Electrophysiol. 2008 Aug;19(8):775-81. doi: 10.1111/j.1540-8167.2008.01140.x. Epub 2008 Mar 26. J Cardiovasc Electrophysiol. 2008. PMID: 18373594
Absence of connexin 40 gene polymorphism, as a marker of undetected atrial fibrillation in patients with unexplained cerebral ischemic events.
Chaldoupi SM, Soedamah-Muthu SS, Regieli J, Werf Cv, Nelen M, van der Smagt JJ, Algra A, Hauer RN, Doevendans PA, Loh P. Chaldoupi SM, et al. Among authors: van der smagt jj. Eur J Cardiovasc Prev Rehabil. 2009 Oct;16(5):616-20. doi: 10.1097/HJR.0b013e32832da03a. Eur J Cardiovasc Prev Rehabil. 2009. PMID: 19494781
Dominant-negative ALK2 allele associates with congenital heart defects.
Smith KA, Joziasse IC, Chocron S, van Dinther M, Guryev V, Verhoeven MC, Rehmann H, van der Smagt JJ, Doevendans PA, Cuppen E, Mulder BJ, Ten Dijke P, Bakkers J. Smith KA, et al. Among authors: van der smagt jj, van dinther m. Circulation. 2009 Jun 23;119(24):3062-9. doi: 10.1161/CIRCULATIONAHA.108.843714. Epub 2009 Jun 8. Circulation. 2009. PMID: 19506109
New ECG criteria in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Cox MG, van der Smagt JJ, Wilde AA, Wiesfeld AC, Atsma DE, Nelen MR, Rodriguez LM, Loh P, Cramer MJ, Doevendans PA, van Tintelen JP, de Bakker JM, Hauer RN. Cox MG, et al. Among authors: van der smagt jj, van tintelen jp. Circ Arrhythm Electrophysiol. 2009 Oct;2(5):524-30. doi: 10.1161/CIRCEP.108.832519. Epub 2009 Jul 7. Circ Arrhythm Electrophysiol. 2009. PMID: 19843920
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study.
Bhuiyan ZA, Jongbloed JD, van der Smagt J, Lombardi PM, Wiesfeld AC, Nelen M, Schouten M, Jongbloed R, Cox MG, van Wolferen M, Rodriguez LM, van Gelder IC, Bikker H, Suurmeijer AJ, van den Berg MP, Mannens MM, Hauer RN, Wilde AA, van Tintelen JP. Bhuiyan ZA, et al. Among authors: van der smagt j, van wolferen m, van den berg mp, van gelder ic, van tintelen jp. Circ Cardiovasc Genet. 2009 Oct;2(5):418-27. doi: 10.1161/CIRCGENETICS.108.839829. Epub 2009 Aug 1. Circ Cardiovasc Genet. 2009. PMID: 20031616
Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteria.
Cox MG, van der Smagt JJ, Noorman M, Wiesfeld AC, Volders PG, van Langen IM, Atsma DE, Dooijes D, Houweling AC, Loh P, Jordaens L, Arens Y, Cramer MJ, Doevendans PA, van Tintelen JP, Wilde AA, Hauer RN. Cox MG, et al. Among authors: van langen im, van der smagt jj, van tintelen jp. Circ Arrhythm Electrophysiol. 2010 Apr;3(2):126-33. doi: 10.1161/CIRCEP.109.927202. Epub 2010 Mar 9. Circ Arrhythm Electrophysiol. 2010. PMID: 20215590
The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.
Hoedemaekers YM, Caliskan K, Michels M, Frohn-Mulder I, van der Smagt JJ, Phefferkorn JE, Wessels MW, ten Cate FJ, Sijbrands EJ, Dooijes D, Majoor-Krakauer DF. Hoedemaekers YM, et al. Among authors: van der smagt jj. Circ Cardiovasc Genet. 2010 Jun;3(3):232-9. doi: 10.1161/CIRCGENETICS.109.903898. Epub 2010 Jun 8. Circ Cardiovasc Genet. 2010. PMID: 20530761
100 results