In 2008, The ESC Working Group on Myocardial and Pericardial Diseases proposed an updated classification of cardiomyopathies based on morphological and functional phenotypes and subcategories of familial/genetic and non-familial/non-genetic disease. In this position statement, we propose a framework for the clinical approach to diagnosis in cardiomyopathies based on the recognition of diagnostic 'red flags' that can be used to guide rational selection of specialized tests including genetic analysis. The basic premise is that the adoption of a cardiomyopathy-specific mindset which combines conventional cardiological assessment with non-cardiac and molecular parameters increases diagnostic accuracy and thus improves advice and treatment for p...
Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases b...
Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases b...
This document describes the contribution of clinical criteria to the interpretation of genetic varia...
In 2008, The ESC Working Group on Myocardial and Pericardial Diseases proposed an updated classifica...
none14siIn 2008, The ESC Working Group on Myocardial and Pericardial Diseases proposed an updated cl...
Advances in molecular genetics present new opportunities and challenges for cardiologists who manage...
Advances in molecular genetics present new opportunities and challenges for cardiologists who manage...
Cardiomyopathies are little known to internists and general practitioners (GPs), and not always able...
Advances in molecular genetics present new opportunities and challenges for cardiologists who manage...
Most cardiomyopathies are familial diseases. Cascade family screening identifies asymptomatic patien...
According to current European classification, cardiomyopathies are defined as myocardial disorders t...
Cardiomyopathies are defined as a myocardial disorder with a structurally and functionally abnormal ...
Cardiomyopathies are myocardial disorders in which the heart muscle is structurally and functionally...
Primary myocardial diseases have always attracted the interest of the scientific community because o...
Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogen...
Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases b...
Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases b...
This document describes the contribution of clinical criteria to the interpretation of genetic varia...
In 2008, The ESC Working Group on Myocardial and Pericardial Diseases proposed an updated classifica...
none14siIn 2008, The ESC Working Group on Myocardial and Pericardial Diseases proposed an updated cl...
Advances in molecular genetics present new opportunities and challenges for cardiologists who manage...
Advances in molecular genetics present new opportunities and challenges for cardiologists who manage...
Cardiomyopathies are little known to internists and general practitioners (GPs), and not always able...
Advances in molecular genetics present new opportunities and challenges for cardiologists who manage...
Most cardiomyopathies are familial diseases. Cascade family screening identifies asymptomatic patien...
According to current European classification, cardiomyopathies are defined as myocardial disorders t...
Cardiomyopathies are defined as a myocardial disorder with a structurally and functionally abnormal ...
Cardiomyopathies are myocardial disorders in which the heart muscle is structurally and functionally...
Primary myocardial diseases have always attracted the interest of the scientific community because o...
Inherited cardiomyopathies include hypertrophic cardiomyopathy, dilated cardiomyopathy, arrhythmogen...
Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases b...
Cardiomyopathies represent a group of diseases of the myocardium of the heart and include diseases b...
This document describes the contribution of clinical criteria to the interpretation of genetic varia...