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 …

[HTML][HTML] T2 mapping in myocardial disease: a comprehensive review

AT O'Brien, KE Gil, J Varghese, OP Simonetti… - Journal of …, 2022 - Elsevier
Cardiovascular magnetic resonance (CMR) is considered the gold standard imaging
modality for myocardial tissue characterization. Elevated transverse relaxation time (T2) is …

High-sensitivity assays for troponin in patients with cardiac disease

D Westermann, JT Neumann, NA Sörensen… - Nature Reviews …, 2017 - nature.com
Troponin is a widely used biomarker in patients with cardiac disease. The use of troponin is
well established in patients with suspected acute myocardial infarction (AMI), but troponin …

[HTML][HTML] Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report

D Corrado, A Anastasakis, C Basso, B Bauce… - International Journal of …, 2024 - Elsevier
Arrhythmogenic cardiomyopathy (ACM) is a heart muscle disease characterized by
prominent “non-ischemic” myocardial scarring predisposing to ventricular electrical …

Native myocardial T1 time can predict development of subsequent anthracycline‐induced cardiomyopathy

F Muehlberg, S Funk, L Zange… - ESC heart …, 2018 - Wiley Online Library
Aims This study aims to assess subclinical changes in functional and morphological
myocardial magnetic resonance parameters very early into an anthracycline treatment …

Cardiac magnetic resonance imaging of arrhythmogenic cardiomyopathy: evolving diagnostic perspectives

A Cipriani, G Mattesi, R Bariani, A Cecere, N Martini… - European …, 2023 - Springer
Arrhythmogenic cardiomyopathy (ACM) is a genetically determined heart muscle disease
characterized by fibro-fatty myocardial replacement, clinically associated with malignant …

Quantification of myocardial strain assessed by cardiovascular magnetic resonance feature tracking in healthy subjects—influence of segmentation and analysis …

C Lim, E Blaszczyk, L Riazy, S Wiesemann… - European …, 2021 - Springer
Objectives Quantification of myocardial deformation by feature tracking is of growing interest
in cardiovascular magnetic resonance. It allows the assessment of regional myocardial …

[HTML][HTML] Myotonic dystrophy type 2: the 2020 update

G Meola - Acta Myologica, 2020 - ncbi.nlm.nih.gov
The myotonic dystrophies are the commonest cause of adult-onset muscular dystrophy.
Phenotypes of DM1 and DM2 are similar, but there are some important differences …

Fatty Infiltration of the Myocardium and Arrhythmogenesis: Potential Cellular and Molecular Mechanisms

JMB Anumonwo, T Herron - Frontiers in physiology, 2018 - frontiersin.org
Anatomical evidence in several species shows highly heterogeneous fat distribution in the
atrial and ventricular myocardium. Atrial appendages have fat deposits, and more so on the …

Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects

G Meola, R Cardani - Neurological Sciences, 2017 - Springer
Myotonic dystrophy (DM) is the most common adult muscular dystrophy, characterized by
autosomal dominant progressive myopathy, myotonia, and multiorgan involvement. To date …