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Circulation. Cardiovascular Genetics|March 1, 2012
Mortality of inherited arrhythmia syndromes: insight into their natural historyEline A Nannenberg, Eric J G Sijbrands, Lea M Dijksman, et al.
Basic Research in Cardiology|April 9, 2015
Complement system modulation as a target for treatment of arrhythmogenic cardiomyopathyManolis Mavroidis, Constantinos H Davos, Stelios Psarras, et al.
Cardiovascular Research|February 28, 2002
Gender differences in the long QT syndrome: effects of beta-adrenoceptor blockadeChantal E Conrath, Arthur A M Wilde, Rosalie J E Jongbloed, et al.
Heart Rhythm|March 30, 2021
Global approaches to cardiogenetic evaluation after sudden cardiac death in the young: A survey among health care professionalsLieke M van den Heuvel, Judy Do, Laura Yeates, et al.
Human Mutation|February 14, 2015
The ARVD/C genetic variants database: 2014 updateElisabetta Lazzarini, Jan D H Jongbloed, Kalliopi Pilichou, et al.
Circulation. Genomic and Precision Medicine|October 20, 2020
Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac ConditionsLieke M van den Heuvel, Maxiem O van Teijlingen, Wilma van der Roest, et al.
ESC Heart Failure|July 17, 2022
Blood-based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta-analysisMark Jansen, Sila Algül, Laurens P Bosman, et al.
Histopathology|March 13, 2016
Phospholamban p.Arg14del cardiomyopathy is characterized by phospholamban aggregates, aggresomes, and autophagic degradationWouter P Te Rijdt, J Peter van Tintelen, Aryan Vink, et al.
Cardiovascular Research|March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kineticsW Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
European Journal of Human Genetics : EJHG|May 5, 2019
Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counseleesLieke M van den Heuvel, Mette J Huisinga, Yvonne M Hoedemaekers, et al.
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