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European Journal of Heart Failure|October 25, 2011
Carriers of the hypertrophic cardiomyopathy MYBPC3 mutation are characterized by reduced myocardial efficiency in the absence of hypertrophy and microvascular dysfunctionStefan A J Timmer, Tjeerd Germans, Wessel P Brouwer, et al.
American Journal of Medical Genetics. Part A|September 9, 2005
Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndromeKarin S W H Hendriks, F J M Grosfeld, J P van Tintelen, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|February 7, 2024
Is it safe to give birth with an activated implantable cardioverter-defibrillator: A multicentre observational studyWilleke van der Stuijt, Kirsten M Kooiman, Jolien A de Veld, et al.
Heart Rhythm|June 10, 2022
Value of genetic testing in the diagnosis and risk stratification of arrhythmogenic right ventricular cardiomyopathyRemco de Brouwer, Laurens P Bosman, Sophia Gripenstedt, et al.
Heart Rhythm|September 16, 2019
Genetic arrhythmias complicating patients with dilated cardiomyopathyZongzhe Li, Peng Chen, Chenze Li, et al.
Hand (New York, N.Y.)|November 27, 2024
Quality, Reliability, and Readability of Peripheral Nerve Intervention Websites for PatientsKeith T Kuo, Kitae Eric Park, Rachana Suresh, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|April 18, 2024
Assessment of ICD eligibility in non-ischaemic cardiomyopathy patients: a position statement by the Task Force of the Dutch Society of CardiologyAnne-Lotte C J van der Lingen, Tom E Verstraelen, Lieselot van Erven, et al.
Forensic Science International|April 10, 2017
Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A geneT Jenewein, B M Beckmann, S Rose, et al.
JACC. Clinical Electrophysiology|May 16, 2018
Treatment of Atrial and Ventricular Arrhythmias Through Autonomic ModulationSébastien P J Krul, Wouter R Berger, Marieke W Veldkamp, et al.
Circulation Research|February 8, 2003
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction systemConnie R Bezzina, Martin B Rook, W Antoinette Groenewegen, et al.
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