Results 141 to 150 of about 462,679 (319)

FDG PET/CT imaging and circulating biomarkers of inflammation in desmoplakin cardiomyopathy

open access: yesESC Heart Failure, Volume 12, Issue 2, Page 1485-1489, April 2025.
Abstract Aims Inflammation has been implicated in the pathogenesis of desmoplakin (DSP) cardiomyopathy, and retrospective studies have described abnormal myocardial fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) findings in symptomatic patients eventually diagnosed with DSP cardiomyopathy.
Sanjay Divakaran   +10 more
wiley   +1 more source

Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes

open access: yesiScience
Summary: Genetic analysis identified the cause of the disease in inherited arrhythmogenic syndromes. A clinically actionable genetic diagnosis requires an accurate interpretation following the current guidelines. Practically half of the genetic diagnoses
Estefanía Martínez-Barrios   +14 more
doaj  

Early Warning System of Sudden Cardiac Death Based on Internet Electrocardiograph and Intelligent Platform

open access: yesZhongguo yiliao qixie zazhi
An early warning system of sudden cardiac death based on the Internet electrocardiograph and intelligent platform is designed to detect the signal of sudden cardiac death in time and save lives.
Yunquan WANG, Tianfa LI, Xun BI
doaj   +1 more source

A Unique Case of Cardiac Arrest following K2 Abuse

open access: yesCase Reports in Cardiology, 2014
Sudden cardiac death (SCD) accounts for up to 450,000 deaths every year in the United States (Zipes et al. (2006)). Most cases of sudden cardiac death occur in subjects with no prior history of heart disease (Myerburg et al. (1998)).
Saif Ibrahim   +2 more
doaj   +1 more source

Role for inflammatory markers in predicting right ventricular failure in mechanical assist device recipients

open access: yesESC Heart Failure, Volume 12, Issue 4, Page 2608-2620, August 2025.
Abstract Right ventricular failure (RVF) is a common complication following left ventricular assist device (LVAD) implantation and increases patient morbidity and mortality. Due to the complex and limited understanding of RVF pathophysiology, efforts to prognosticate RVF after LVAD have been challenging.
Abdul‐Fatawu Osman   +11 more
wiley   +1 more source

Discovering new hub genes of dilated cardiomyopathy

open access: yesESC Heart Failure, Volume 12, Issue 4, Page 2487-2498, August 2025.
Abstract Aims Dilated cardiomyopathy (DCM) has a poor prognosis and exhibits a complex and diverse aetiology and genetic profile. The genes responsible for the pathogenesis of DCM have not been fully identified. The present study aimed to explore new hub genes of DCM by mining the human DCM databases and further by experimental validation.
Jun‐Yan Zhu   +9 more
wiley   +1 more source

Spotlight on sudden arrhythmic death syndrome

open access: yesResearch Reports in Clinical Cardiology, 2019
David Yuan,1 Hariharan Raju1,2 1Cardiology Department, Concord Repatriation General Hospital, Sydney, Australia; 2Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, AustraliaCorrespondence: Hariharan RajuCardiology Department,
Yuan D, Raju H
doaj  

T1 mapping and major cardiovascular events in non‐ischaemic dilated cardiomyopathy: a systematic review and meta‐analysis

open access: yesESC Heart Failure, Volume 12, Issue 4, Page 2621-2630, August 2025.
In NIDCM patients, native T1 mapping and ECV were associated with increased risk of the composite primary endpoint of MACE and the secondary endpoint of heart failure and arrhythmic‐related events. Patients who experienced MACE had higher values of both T1 mapping and ECV.
Federico Marchini   +9 more
wiley   +1 more source

Association single nucleotide polymorphisms of gene lipid metabolism APOE, HL, SREBP2, USF1 with sudden cardiac death by russian population

open access: yesАтеросклероз, 2014
Study objective. Investigate the association of polymorphisms E2/E3/E4 gene APOE, rs1800588 gene HL, rs2228314 gene SREBP2, rs2516839 gene USF1 with sudden cardiac death in the Russian population. Materials and methods.
V. N. Maksimov   +6 more
doaj  

The analysis of sudden cardiac death cases among young persons in the Dnepropetrovsk region [PDF]

open access: yesМорфологія, 2013
The purpose of studying is investigation of frequency and structure of the sudden cardiac death reasons among young persons in Dnepropetrovsk region. We had been carried out the retrospective analysis of 1765 of sudden cardiac death cases among persons ...
Nekhanevich OB, Voichenko VV
doaj  

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