Results 101 to 110 of about 32,760 (223)

Relationship Between Electrocardiographic Findings and Cardiac Magnetic Resonance Phenotypes in Arrhythmogenic Cardiomyopathy

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2018
Background The new designation of arrhythmogenic cardiomyopathy defines a broader spectrum of disease phenotypes, which include right dominant, biventricular, and left dominant variants. We evaluated the relationship between electrocardiographic findings
Manuel De Lazzari, Alessandro Zorzi, Alberto Cipriani, Angela Susana, Giulio Mastella, Alessandro Rizzo, Ilaria Rigato, Barbara Bauce, Benedetta Giorgi, Carmelo Lacognata, Sabino Iliceto, Domenico Corrado, Martina Perazzolo Marra   +12 more
doaj   +1 more source

Rabbit models of heart disease. [PDF]

, 2008
Human heart disease is a major cause of death and disability. A variety of animal models of cardiac disease have been developed to better understand the etiology, cellular and molecular mechanisms of cardiac dysfunction and novel therapeutic strategies ...
Bers, Donald M, Pogwizd, Steven M
core  

Genomic insights into cardiomyopathies: a comparative cross-species review [PDF]

, 2017
n the global human population, the leading cause of non-communicable death is cardiovascular disease. It is predicted that by 2030, deaths attributable to cardiovascular disease will have risen to over 20 million per year.
Beffagna, Carrier, Cruz, Elliott, Fox, Fox, Gallego-Delgado, Hilfiker-Kleiner, Huang, Inagaki, Kimura, Kucerova, Lacuata, Maekawa, Maron, Meurs, Niss, Qu, Sakamoto, Sandusky, Wang, Zeviani   +21 more
core   +1 more source

Left Bundle Branch Area Pacing Reverts Electromechanical Window Negativity to a Similar Extent as Biventricular Pacing

Pacing and Clinical Electrophysiology, EarlyView.
BiVP = biventricular pacing; CRT = cardiac resynchronization therapy; EMW = electromechanical window; LBBAP = left bundle branch area pacing; QAoC = Time interval from the onset of the QRS complex to the center of the aortic valve closure artifact; QT = QT interval measured by tangent method.
Florien Klein, Metra Daliry, Karin C. Smits, Edoardo Bressi, Peter M. Deissler, Johan van Koll, Jesse H. J. Rijks, Antonius M. W. van Stipdonk, Rachel M. A. ter Bekke, Domenico Grieco, Chiara Manfuro, Giorgia Spiridigliozzi, Annalisa Casalese, Justin G. L. M. Luermans, Frits W. Prinzen, Roel Meiburg, Leonard M. Rademakers, Kevin Vernooy, Uyên Châu Nguyên   +18 more
wiley   +1 more source

Lifestyle modification in atrial fibrillation: Mechanisms, phenotypes and ablation outcomes

Experimental Physiology, EarlyView.
Abstract Atrial fibrillation (AF) is the most prevalent sustained cardiac arrhythmia and is associated with significant morbidity, mortality and healthcare utilization. Catheter ablation is increasingly used as a rhythm‐control intervention for patients with symptomatic paroxysmal and persistent AF, yet recurrence rates remain suboptimal.
Konstantinos Grigoriou, Paschalis Karakasis, Panagiotis Theofilis, Konstantinos Pamporis, Panayotis K. Vlachakis, Anastasios Apostolos, Nikolaos Ktenopoulos, Barbara Fyntanidou, Efstratios Karagiannidis, Dimitrios Patoulias, Antonios P Antoniadis, Nikolaos Fragakis   +11 more
wiley   +1 more source

Recurrent Syncope in a Young Man: What Lies Underneath?

Indian Journal of Clinical Cardiology
Arrhythmogenic right ventricular cardiomyopathy is an autosomal dominant genetic disease which leads to fatty replacement of the right ventricular myocardium, leading to the occurrence of ventricular arrhythmia.
Deepanjan Bhattacharya, Koyel Chakraborty, Ajay Gautam, Basudeb Bhattacharjee   +3 more
doaj   +1 more source

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures. [PDF]

, 2018
OBJECTIVES: The purpose of this study was to assess the phenotype of Filamin C (FLNC) truncating variants in dilated cardiomyopathy (DCM) and understand the mechanism leading to an arrhythmogenic phenotype. BACKGROUND: Mutations in FLNC are known to lead
Abecasis, Asimaki, Asimaki, Asimaki, Begay, Brodehl, Campbell, Chelko, Daughenbaugh, Deo, Furst, Golbus, Gontier, Haas, Hershberger, Kley, Kley, Landrum, Lek, Liu, Marcus, Mestroni, Ortiz-Genga, Rowland, Spezzacatene, Valdes-Mas, van, Wang, Wu, Zhou   +29 more
core   +2 more sources

Arrhythmogenic left ventricular cardiomyopathy

BJR|case reports, 2020
Arrhythmogenic ventricular cardiomyopathy (AVC) is a heritable heart muscle disorder characterized by fibrofatty infiltration of the myocardium. Intramyocardial fat deposition is considered arrhythmogenic and predisposes patients to life-threatening arrhythmias and sudden cardiac death.
Mirmomen, Seyedeh Mojdeh, Bradley, Andrew Jay, Arai, Andrew Ernest, Sirajuddin, Arlene   +3 more
openaire   +2 more sources

Cardiac remodelling in type 2 diabetes: Pathophysiological mechanisms and opportunities for multiscale computational modelling and simulation

The Journal of Physiology, EarlyView.
Abstract figure legend Overview of multiscale cardiac remodelling in type 2 diabetes and how to model and simulate these changes using a human‐based, multiscale computational framework. Cardiac remodelling in type 2 diabetes occurs at ionic channel, protein, cellular, tissue and whole‐organ level, affecting the electrophysiological function, mechanical
Ambre Bertrand, Jakub Tomek, Blanca Rodriguez   +2 more
wiley   +1 more source

Sudden cardiac death in patients with nonischemic cardiomyopathy

Indian Heart Journal, 2014
Sudden cardiac death (SCD) is an important cause of mortality worldwide. Although SCD is most often associated with coronary heart disease, the risk of SCD in patients without ischemic heart disease is well-established.
Brian P. Betensky, Sanjay Dixit
doaj   +1 more source