Genetics of dilated cardiomyopathy
S Kärkkäinen, K Peuhkurinen - Annals of medicine, 2007 - Taylor & Francis
Dilated cardiomyopathy (DCM) is a myocardial disease characterized by dilatation and
impaired systolic function of the left or both ventricles. The etiology of DCM is multifactorial …
impaired systolic function of the left or both ventricles. The etiology of DCM is multifactorial …
Genetics of dilated cardiomyopathy
Y Fu, HJ Eisen - Current cardiology reports, 2018 - Springer
Abstract Purpose of Review Dilated cardiomyopathy (DCM) is characterized by left
ventricular dilation and systolic function and is the most common among all …
ventricular dilation and systolic function and is the most common among all …
Genetics of dilated cardiomyopathy
D Fatkin, R Otway, Z Richmond - Heart Failure Clinics, 2010 - heartfailure.theclinics.com
Dilated cardiomyopathy (DCM) is a myocardial disorder defined by ventricular chamber
enlargement and systolic dysfunction that can result in progressive heart failure …
enlargement and systolic dysfunction that can result in progressive heart failure …
Genetics of dilated cardiomyopathy
SN Chen, L Mestroni, MRG Taylor - Current opinion in cardiology, 2021 - journals.lww.com
The identification of the molecular causes and subsequent insight into the molecular
mechanisms of DCM is expanding our understanding of DCM pathogenesis and highlights …
mechanisms of DCM is expanding our understanding of DCM pathogenesis and highlights …
Genetics of dilated cardiomyopathy: clinical implications
A Paldino, G De Angelis, M Merlo, M Gigli… - Current cardiology …, 2018 - Springer
Abstract Purpose of Review This review aims to summarize the current knowledge on the
genetic background of dilated cardiomyopathy (DCM), with particular attention to the …
genetic background of dilated cardiomyopathy (DCM), with particular attention to the …
[HTML][HTML] Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals
RE Hershberger, A Morales, JD Siegfried - Genetics in Medicine, 2010 - Elsevier
Dilated cardiomyopathy (DCM), usually diagnosed as idiopathic dilated cardiomyopathy
(IDC), has been shown to have a familial basis in 20–35% of cases. Genetic studies in …
(IDC), has been shown to have a familial basis in 20–35% of cases. Genetic studies in …
Current perspective new insights into the molecular basis of familial dilated cardiomyopathy.
G Sinagra, A Di Lenarda, GL Brodsky… - Italian Heart Journal …, 2001 - europepmc.org
Genetic disease transmission has been identified in a significant proportion of patients with
dilated cardiomyopathy (DCM). Variable clinical characteristics and patterns of inheritance …
dilated cardiomyopathy (DCM). Variable clinical characteristics and patterns of inheritance …
Guidelines for the diagnosis and management of familial dilated cardiomyopathy
D Fatkin… - Heart, Lung and …, 2011 - Elsevier
Dilated cardiomyopathy (DCM) is a myocardial disorder that is a major cause of heart failure
and death. Recent data indicate that genetic factors are important in the pathogenesis of …
and death. Recent data indicate that genetic factors are important in the pathogenesis of …
[HTML][HTML] Dilated cardiomyopathy overview
RE Hershberger, E Jordan - 2022 - europepmc.org
Dilated Cardiomyopathy Overview - Abstract - Europe PMC Sign in | Create an account https://orcid.org
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Hereditary dilated cardiomyopathy
TR Mcminn Jr, J Ross Jr - Clinical cardiology, 1995 - Wiley Online Library
Dilated cardiomyopathy (DCM) is a common and important cause of morbidity and mortality.
Many factors can contribute to the development of this disorder, although most commonly …
Many factors can contribute to the development of this disorder, although most commonly …