Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
European Heart Journal. Case Reports|November 18, 2020
Case report: spontaneous coronary artery dissection and suspicion of takotsubo cardiomyopathy in a patient presenting with T-wave inversions, severe QTc prolongation, elevated cardiac biomarkers, and apical akinesiaKåre Peter Frederiksen, Helle Søholm, Ole Havndrup, et al.
Ugeskrift for Laeger|January 19, 2011
[Another genetic cause of sudden cardiac death]Daniel Vega Møller, Lars Køber, Ole Havndrup, et al.
Cardiovascular Research|February 5, 2003
Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutationsOle Havndrup, Henning Bundgaard, Paal Skytt Andersen, et al.
The International Journal of Cardiovascular Imaging|August 2, 2015
Echocardiographic evaluation of pre-diagnostic development in young relatives genetically predisposed to hypertrophic cardiomyopathyMorten K Jensen, Ole Havndrup, Michael Christiansen, et al.
Scandinavian Cardiovascular Journal : SCJ|May 25, 2011
Survival and sudden cardiac death after septal ablation for hypertrophic obstructive cardiomyopathyMorten Kvistholm Jensen, Ole Havndrup, Christian Hassager, et al.
European Journal of Human Genetics : EJHG|October 16, 2004
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod regionLotte Hougs, Ole Havndrup, Henning Bundgaard, et al.
Ugeskrift for Laeger|July 11, 2006
[Long QT syndrome--genes, mechanisms and risks. Indication for genetic family screening?]Henning Bundgaard, Ole Havndrup, Michael Christiansen, et al.
Circulation|December 1, 2012
Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testingMorten K Jensen, Ole Havndrup, Michael Christiansen, et al.
European Journal of Human Genetics : EJHG|April 29, 2004
Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiencyPaal S Andersen, Ole Havndrup, Henning Bundgaard, et al.
Heart (British Cardiac Society)|December 15, 2015
Functional effects of losartan in hypertrophic cardiomyopathy-a randomised clinical trialAnna Axelsson, Kasper Iversen, Niels Vejlstrup, et al.
Pageof 3