This review article discusses the genetic bases of cardiac arrest with a specific focus on cardiac channelopathies and right ventricular cardiomyopathy. We review the appropriate use of genetic testing in those patients suspected to have inherited cardiac arrhythmias, highlighting the importance of most genotype-phenotype correlations for risk stratification. The article also presents the most recent views on diagnostic criteria and flowcharts for treatment of patients with inherited arrhythmogenic diseases
Thanks to the contribution of molecular genetics, the genetic bases, the pathogenesis and genotype-p...
Genetic approaches have succeeded in defining the molecular basis of an increasing array of heart di...
Up to 14,500 young individuals die suddenly every year in Europe of cardiac pathologies. The majorit...
In this article we will review the appropriate use of genetic testing in those patients suspected of...
Inherited primary arrhythmia syndromes are genetically determined disorders of cardiac ion channels ...
In the past decade, the discovery that cases of ventricular arrhythmias and sudden cardiac death (SC...
PURPOSE OF REVIEW: The current article provides a concise summary of the possibilities and limit...
There have been remarkable advances in our knowledge of the underlying heritability of cardiac arrhy...
PURPOSE OF REVIEW: In this article, we discuss the most recent and relevant studies published in...
A variety of arrhythmogenic cardiac diseases such as channelopathies and cardiomyopathies are caused...
Cardiac channelopathies are linked to an increased risk of ventricular arrhythmia and sudden death. ...
Continued research into the identification of mutated genes that cause inherited arrhythmogenic dise...
Genetic analysis can be performed to identify the molecular substrate of inherited arrhythmogenic di...
There are few areas in cardiology in which the impact of genetics and genetic testing on clinical ma...
AbstractInherited arrhythmias, such as cardiomyopathies and cardiac ion channelopathies, along with ...
Thanks to the contribution of molecular genetics, the genetic bases, the pathogenesis and genotype-p...
Genetic approaches have succeeded in defining the molecular basis of an increasing array of heart di...
Up to 14,500 young individuals die suddenly every year in Europe of cardiac pathologies. The majorit...
In this article we will review the appropriate use of genetic testing in those patients suspected of...
Inherited primary arrhythmia syndromes are genetically determined disorders of cardiac ion channels ...
In the past decade, the discovery that cases of ventricular arrhythmias and sudden cardiac death (SC...
PURPOSE OF REVIEW: The current article provides a concise summary of the possibilities and limit...
There have been remarkable advances in our knowledge of the underlying heritability of cardiac arrhy...
PURPOSE OF REVIEW: In this article, we discuss the most recent and relevant studies published in...
A variety of arrhythmogenic cardiac diseases such as channelopathies and cardiomyopathies are caused...
Cardiac channelopathies are linked to an increased risk of ventricular arrhythmia and sudden death. ...
Continued research into the identification of mutated genes that cause inherited arrhythmogenic dise...
Genetic analysis can be performed to identify the molecular substrate of inherited arrhythmogenic di...
There are few areas in cardiology in which the impact of genetics and genetic testing on clinical ma...
AbstractInherited arrhythmias, such as cardiomyopathies and cardiac ion channelopathies, along with ...
Thanks to the contribution of molecular genetics, the genetic bases, the pathogenesis and genotype-p...
Genetic approaches have succeeded in defining the molecular basis of an increasing array of heart di...
Up to 14,500 young individuals die suddenly every year in Europe of cardiac pathologies. The majorit...