Last Posted: Jun 24, 2019
- European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
F Fellmann et al, EJHG, June 24, 2019 - Fabry disease in cardiology practice: Literature review and expert point of view.
Hagège Albert et al. Archives of cardiovascular diseases 2019 Apr 112(4) 278-287 - Cases in Precision Medicine: Genetic Assessment After a Sudden Cardiac Death in the Family.
Laracuente Ronald et al. Annals of internal medicine 2019 May - Inherited cardiomyopathies.
Miles Chris et al. BMJ (Clinical research ed.) 2019 365l1570 - Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation.
Headrick Andrew T et al. Molecular genetics & genomic medicine 2019 Apr e593 - It took more than a decade to explain the sudden death of my precious teenage son
K Gardner, the Guardian, February 22, 2019 - Genetic Aspects of Hereditary Arrhythmogenic Syndromes in Children and Adults.
Miranovic Vesna et al. Acta clinica Croatica 2017 Dec 56(4) 749-755 - Sudden unexplained death in the young: epidemiology, aetiology and value of the clinically guided genetic screening.
Anastasakis Aris et al. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2018 20(3) 472-480 - The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry.
Roston Thomas M et al. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2018 20(3) 541-547 - Follow-up of fatty acid β-oxidation disorders in expanded newborn screening era.
Janeiro Patrícia et al. European journal of pediatrics 2019 Jan
No hay comentarios:
Publicar un comentario