2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association for Cardio-Thoracic Surgery …

G Hindricks, T Potpara, N Dagres, E Arbelo… - European heart …, 2021 - academic.oup.com
MicroRNAs (miRNAs) are small regulatory molecules post-transcriptionally suppressing
mRNA activity. Many miRNAs in various organisms have been cloned but many unknown …

Skeletal and cardiac muscle disorders caused by mutations in genes encoding intermediate filament proteins

L Maggi, M Mavroidis, S Psarras, Y Capetanaki… - International Journal of …, 2021 - mdpi.com
Intermediate filaments are major components of the cytoskeleton. Desmin and synemin,
cytoplasmic intermediate filament proteins and A-type lamins, nuclear intermediate filament …

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 …

Risk predictors in a Spanish cohort with cardiac laminopathies. The REDLAMINA registry

R Barriales-Villa, JP Ochoa… - Revista Española de …, 2021 - Elsevier
Introduction and objectives According to sudden cardiac death guidelines, an implantable
cardioverter-defibrillator (ICD) should be considered in patients with LMNA-related dilated …

Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences

CR Vissing, TB Rasmussen, AM Dybro… - Journal of Medical …, 2021 - jmg.bmj.com
Background Truncating variants in titin (TTNtv) are the most common cause of dilated
cardiomyopathy (DCM). We evaluated the genotype-phenotype correlation in TTNtv-DCM …

Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients

Y Fan, D Tan, D Song, X Zhang, X Chang… - Journal of Medical …, 2021 - jmg.bmj.com
Background LMNA-related muscular dystrophy is caused by mutations in LMNA gene. We
aimed to identify genetic variations and clinical features in a large cohort of Chinese patients …

[HTML][HTML] Genetics of cardiomyopathy: clinical and mechanistic implications for heart failure

KH Kim, NL Pereira - Korean Circulation Journal, 2021 - ncbi.nlm.nih.gov
Genetics has played an important role in the understanding of different cardiomyopathies,
and the field of heart failure (HF) genetics is progressing rapidly. Much research has also …

Clinical features of LMNA-related cardiomyopathy in 18 patients and characterization of two novel variants

V Ferradini, J Cosma, F Romeo, C De Masi… - Journal of Clinical …, 2021 - mdpi.com
Dilated cardiomyopathy (DCM) refers to a spectrum of heterogeneous myocardial disorders
characterized by ventricular dilation and depressed myocardial performance in the absence …

Considering complexity in the genetic evaluation of dilated cardiomyopathy

E Jordan, RE Hershberger - Heart, 2021 - heart.bmj.com
Dilated cardiomyopathy (DCM) is a cardiovascular disease of genetic aetiology that causes
substantial morbidity and mortality, and presents considerable opportunity for disease …

Circulating circRNA as biomarkers for dilated cardiomyopathy etiology

MC Costa, M Calderon-Dominguez, A Mangas… - Journal of Molecular …, 2021 - Springer
Dilated cardiomyopathy (DCM) is the third most common cause of heart failure. The
multidisciplinary nature of testing—involving genetics, imaging, or cardiovascular …