2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed by the task force for the …

K Zeppenfeld, J Tfelt-Hansen, M De Riva… - European heart …, 2022 - academic.oup.com
4004 ESC Guidelines label use of medication should be limited to situations where it is in
the patient's interest to do so, with regard to the quality, safety, and efficacy of care, and only …

2021 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy: Developed by the Task Force on cardiac pacing and cardiac resynchronization …

M Glikson, JC Nielsen, MB Kronborg, Y Michowitz… - EP …, 2022 - academic.oup.com
for digital applications (smartphones, etc.). These versions are abridged and thus, for more
detailed information, the user should always access to the full text version of the guidelines …

Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the …

YM Pinto, PM Elliott, E Arbustini, Y Adler… - European heart …, 2016 - academic.oup.com
In this paper the Working Group on Myocardial and Pericardial Disease proposes a revised
definition of dilated cardiomyopathy (DCM) in an attempt to bridge the gap between our …

Management of cardiac involvement associated with neuromuscular diseases: a scientific statement from the American Heart Association

B Feingold, WT Mahle, S Auerbach, P Clemens… - Circulation, 2017 - Am Heart Assoc
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of
morbidity and mortality. The management of cardiac disease in NMDs is made challenging …

Long-term outcome and risk stratification in dilated cardiolaminopathies

M Pasotti, C Klersy, A Pilotto, N Marziliano… - Journal of the American …, 2008 - jacc.org
Objectives: The aim of this study was to analyze the long-term follow-up of dilated
cardiolaminopathies. Background: Lamin A/C (LMNA) gene mutations cause a variety of …

Genotype-phenotype correlations in human diseases caused by mutations of LINC complex-associated genes: a systematic review and meta-summary

EC Storey, HR Fuller - Cells, 2022 - mdpi.com
Mutations in genes encoding proteins associated with the linker of nucleoskeleton and
cytoskeleton (LINC) complex within the nuclear envelope cause different diseases with …

The laminopathies: a clinical review

J Rankin, S Ellard - Clinical genetics, 2006 - Wiley Online Library
The laminopathies are a diverse group of conditions caused by mutations in the LMNA gene
(MIM* 150330). LMNA encodes the nuclear envelope proteins lamin A and lamin C by …

Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders

F Anselme, G Moubarak, A Savouré, B Godin, B Borz… - Heart rhythm, 2013 - Elsevier
Background Sudden cardiac death is frequent in patients with lamin A/C gene (LMNA)
mutations and may be related to ventricular arrhythmias (VA). Objective To evaluate a …

Nesprin-1 mutations in human and murine cardiomyopathy

MJ Puckelwartz, EJ Kessler, G Kim, MM DeWitt… - Journal of molecular and …, 2010 - Elsevier
Mutations in LMNA, the gene encoding the nuclear membrane proteins, lamins A and C,
produce cardiac and muscle disease. In the heart, these autosomal dominant LMNA …

2022 HRS expert consensus statement on evaluation and management of arrhythmic risk in neuromuscular disorders

WJ Groh, D Bhakta, GF Tomaselli, RG Aleong… - Heart Rhythm, 2022 - Elsevier
This international multidisciplinary document is intended to guide electrophysiologists,
cardiologists, other clinicians, and health care professionals in caring for patients with …