Results 151 to 160 of about 462,679 (319)
Abstract Aims Hypertrophic cardiomyopathy (HCM) is a rare genetic heart disease characterized by a limited patient population and scarce research and treatment resources. This study aimed to identify HCM‐associated proteins by integrating cardiac tissue data from the Gene Expression Omnibus (GEO) database with the latest protein quantitative trait ...
Bo Li, Xu Zhao, Yan Ding, Yi Zhang
wiley +1 more source
Sudden cardiac death and valvular pathology
Sudden death due to valvular heart disease is reported to range from 1% to 5% in native valves and around 0.2%–0.9%/year in prosthesis. The nature of the diseases is varied, from heritable, congenital to acquired.
Rosa H. A. M. Henriques de Gouveia+1 more
doaj +1 more source
Loss of muscleblind-like 1 results in cardiac pathology and persistence of embryonic splice isoforms. [PDF]
Cardiac dysfunction is a prominent cause of mortality in myotonic dystrophy I (DM1), a disease where expanded CUG repeats bind and disable the muscleblind-like family of splice regulators.
Choi, Jongkyu+8 more
core
Abstract Aims Plasma volume status (PVS) is recognized as a marker of systemic congestion, but its clinical utility in patients with mitral regurgitation (MR) undergoing transcatheter edge‐to‐edge mitral valve repair (M‐TEER) has not been well established. This study aimed to evaluate the prognostic significance of PVS in these patients.
Ai Kagase+30 more
wiley +1 more source
Clinical characteristics and long‐term outcomes in patients with apical hypertrophic cardiomyopathy
Abstract Aims As a special type of hypertrophic cardiomyopathy (HCM), apical HCM (ApHCM) has different clinical characteristics while its nature history and prognosis are not well recognized. We aimed to describe the characteristics and outcomes of ApHCM and identify predictors of adverse outcomes.
Meng Guo+3 more
wiley +1 more source
Idiopathic Submitral Left Ventricular Aneurysm: an Unusual Substrate for Ventricular Tachycardia in Caucasians [PDF]
Annular submitral aneurysms have been rarely reported in Caucasians. They are typically diagnosed in non-white adults who present with severe mitral regurgitation, heart failure, systemic embolism, ventricular arrhythmias, and sudden cardiac death.
Arash, Arya+3 more
core
Prognostic value of left atrial strain in acute and chronic heart failure: A meta‐analysis
The prognostic evaluation of heart failure (HF) beyond ejection fraction remains challenging. Moreover, reliable prognosticators in chronic HF sometimes lose their value in acute settings or vice versa. Speckle tracking echocardiography offers new sensitive parameters for prognostic stratification in heart failure with reduced and preserved ejection ...
Maria Concetta Pastore+12 more
wiley +1 more source
Cardiac sarcoidosis causing sudden death
Sarcoidosis is a systemic disease of young adults. Cardiac involvement is rarely diagnosed clinically. In most cases it presents with arrhythmias and conduction disorders.
Suranagi Vijayalaxmi+2 more
doaj
The story of Christian Eriksen. To close the loop
Dear Editor, On June 12, 2021, Christian Eriksen's life took an unexpected turn when he suffered a cardiac arrest during a match.1Thanks to the swift and skilled actions of medical personnel who administered Cardiopulmonary Resuscitation (CPR), Eriksen ...
Gian Domenico Giusti, Nicola Ramacciati
doaj +1 more source
Acute myocarditis according to age: Presentation, management and early outcomes
MIS, multisystem inflammatory syndrome; MRE, myocarditis‐related events (within 30 days included all‐cause death, cardiogenic shock, cardiac arrest, ventricular arrhythmias or complete AV block). Abstract Aims Acute myocarditis (AM) is a rare but severe disease affecting patients of all ages. Large multicentric studies comparing children and adults are
Clément Karsenty+25 more
wiley +1 more source