Cardiomyopathies and related changes in contractility of human heart muscle

PG Vikhorev, NN Vikhoreva - International journal of molecular sciences, 2018 - mdpi.com
About half of hypertrophic and dilated cardiomyopathies cases have been recognized as
genetic diseases with mutations in sarcomeric proteins. The sarcomeric proteins are …

Transthoracic Echocardiographic Assessment of the Heart in Pregnancy—a position statement on behalf of the British Society of Echocardiography and the United …

SL Curtis, M Belham, S Bennett, R James… - Echo Research & …, 2023 - Springer
Pregnancy is a dynamic process associated with profound hormonally mediated
haemodynamic changes which result in structural and functional adaptations in the …

Mathematical modeling of cardiac function to evaluate clinical cases in adults and children

S Bozkurt - PloS one, 2019 - journals.plos.org
Time-varying elastance models can simulate only the pressure and volume signals in the
heart chambers while the diagnosis of clinical cases and evaluation of different treatment …

Prevalence of cardiac comorbidities, and their underdetection and contribution to exertional symptoms in COPD: results from the COSYCONET cohort

P Alter, BA Mayerhofer, K Kahnert, H Watz… - … Journal of Chronic …, 2019 - Taylor & Francis
Background A substantial prevalence of cardiovascular disease is known for COPD, but
detection of its presence, relationship to functional findings and contribution to symptoms …

Position statement on indications of echocardiography in adults-2019

SH Barberato, MMD Romano, ALS Beck… - Arquivos Brasileiros …, 2019 - SciELO Brasil
In accordance with the “Standards for the Elaboration of Guidelines, Positions and
Normations” sanctioned by the Brazilian Society of Cardiology, this document was written to …

Epidemiology and clinical aspects of genetic cardiomyopathies

D Masarone, JP Kaski, G Pacileo… - Heart Failure …, 2018 - heartfailure.theclinics.com
Cardiomyopathies (CMPs) are myocardial disorders in which the heart muscle is structurally
and functionally abnormal in the absence of abnormal conditions that can explain the …

Multi-modality imaging in dilated cardiomyopathy: with a focus on the role of cardiac magnetic resonance

P Mitropoulou, G Georgiopoulos, S Figliozzi… - Frontiers in …, 2020 - frontiersin.org
Heart failure (HF) is recognized as a leading cause of morbidity and mortality worldwide.
Dilated cardiomyopathy (DCM) is a common phenotype in patients presenting with HF …

[HTML][HTML] Automated quantification of myocardial tissue characteristics from native T1 map** using neural networks with uncertainty-based quality-control

E Puyol-Antón, B Ruijsink, CF Baumgartner… - Journal of …, 2020 - Elsevier
Background Tissue characterisation with cardiovascular magnetic resonance (CMR)
parametric map** has the potential to detect and quantify both focal and diffuse alterations …

Hypertrophic, dilated, and arrhythmogenic cardiomyopathy: where are we?

H El Hadi, A Freund, S Desch, H Thiele, N Majunke - Biomedicines, 2023 - mdpi.com
Cardiomyopathies are a heterogeneous group of structural, mechanical, and electrical heart
muscle disorders which often correlate with life-threatening arrhythmias and progressive …

[HTML][HTML] A comprehensive outlook on dilated cardiomyopathy (DCM): state-of-the-art developments with special emphasis on OMICS-based approaches

V Sarohi, S Srivastava, T Basak - Journal of Cardiovascular Development …, 2022 - mdpi.com
Dilated cardiomyopathy (DCM) remains an enigmatic cardiovascular disease (CVD)
condition characterized by contractile dysfunction of the myocardium due to dilation of the …