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The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J. Winkel BG, et al. Among authors: jensen hk. J Cardiovasc Electrophysiol. 2012 Oct;23(10):1092-8. doi: 10.1111/j.1540-8167.2012.02371.x. Epub 2012 Aug 6. J Cardiovasc Electrophysiol. 2012. PMID: 22882672
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK. Christiansen M, et al. Among authors: jensen hk. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.
The diagnostic performance of imaging methods in ARVC using the 2010 Task Force criteria.
Borgquist R, Haugaa KH, Gilljam T, Bundgaard H, Hansen J, Eschen O, Jensen HK, Holst AG, Edvardsen T, Svendsen JH, Platonov PG. Borgquist R, et al. Among authors: jensen hk. Eur Heart J Cardiovasc Imaging. 2014 Nov;15(11):1219-25. doi: 10.1093/ehjci/jeu109. Epub 2014 Jun 17. Eur Heart J Cardiovasc Imaging. 2014. PMID: 24939949
Heart transplantation in arrhythmogenic right ventricular cardiomyopathy - Experience from the Nordic ARVC Registry.
Gilljam T, Haugaa KH, Jensen HK, Svensson A, Bundgaard H, Hansen J, Dellgren G, Gustafsson F, Eiskjær H, Andreassen AK, Sjögren J, Edvardsen T, Holst AG, Svendsen JH, Platonov PG. Gilljam T, et al. Among authors: jensen hk. Int J Cardiol. 2018 Jan 1;250:201-206. doi: 10.1016/j.ijcard.2017.10.076. Epub 2017 Oct 21. Int J Cardiol. 2018. PMID: 29107359
324 results