Results 101 to 110 of about 261,206 (349)

Metabolic changes during cardiac regeneration in the axolotl

Developmental Dynamics, EarlyView.
Abstract Background The axolotl is a prominent model organism of heart regeneration due to its ability to anatomically and functionally repair the heart after an injury that mimics human myocardial infarction. In humans, such an injury leads to permanent scarring. Cardiac regeneration has been linked to metabolism and the oxygenation state, but so far,
Anita Dittrich, Sofie Amalie Andersson, Morten Busk, Kasper Hansen, Casper Bindzus Foldager, Johan Palmfeldt, Asger Andersen, Michael Pedersen, Mikkel Vendelbo, Kirstine Lykke Nielsen, Henrik Lauridsen   +10 more
wiley   +1 more source

Mitochondrial DNA polymorphisms in individuals died from sudden cardiac death

Фундаментальная и клиническая медицина, 2019
Aim. To identify associations of mtDNA polymorphisms with sudden cardiac death.Materials and Methods. DNA was isolated from the cardiac tissue excised during the autopsy from individuals who died from sudden cardiac death (n = 260).
M. V. Golubenko, A. V. Tsepokina, R. R. Salakhov, V. N. Maksimov, A. A. Gurazheva, B. A. Tkhorenko, A. V. Ponasenko   +6 more
doaj   +1 more source

942-41 Dysplasia of the Atrioventricular Nodal Artery in Patients with Mitral Valve Prolapse and Sudden Cardiac Death [PDF]

, 1995
Patients with isolated mitral valve prolapse (MVP) without significant mitral regurgitation are at a slightly increased risk of sudden cardiac death compared to the normal population. The mechanism(s) of sudden cardiac death in isolated MVP are uncertain.
Burke, Allen P., Farb, Andrew, Rabin, Ira, Tang, Anita L., Virmani, Renu   +4 more
core   +1 more source

Autopsy findings in cases of fatal COVID‐19 vaccine‐induced myocarditis

ESC Heart Failure, EarlyView.
Abstract COVID‐19 vaccines have been linked to myocarditis, which, in some circumstances, can be fatal. This systematic review aims to investigate potential causal links between COVID‐19 vaccines and death from myocarditis using post‐mortem analysis.
Nicolas Hulscher, Roger Hodkinson, William Makis, Peter A. McCullough   +3 more
wiley   +1 more source

Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population [PDF]

, 2020
Background: Triadin knockout syndrome (TKOS) is a potentially lethal arrhythmia disorder caused by recessively inherited null variants in TRDN-encoded cardiac triadin.
Ackerman, MJ, Bagnall, RD, Behr, ER, Clemens, DJ, Dotzler, SM, Giudicessi, JR, Gray, B, Matthews, E, Semsarian, C, Tester, DJ   +9 more
core   +2 more sources

The difficult discussion on the deactivation of implantable cardioverter devices at the end of life: a systematic review

ESC Heart Failure, Volume 12, Issue 2, Page 733-760, April 2025.
Abstract Implantable cardioverter defibrillators (ICDs) reliably prevent death due to life‐threatening arrhythmias; this may become less relevant in people with more severe heart failure who are reaching the end of life (EOL). This review aimed to explore the ICD deactivation process and identify ethical issues, especially around the initiation of ...
Siobhan C. Murray, Claire McNamara, Anna V. Chatzi   +2 more
wiley   +1 more source

Entropy of seismic electric signals: Analysis in natural time under time-reversal [PDF]

, 2005
Electric signals have been recently recorded at the Earth's surface with amplitudes appreciably larger than those hitherto reported. Their entropy in natural time is smaller than that, $S_u$, of a ``uniform'' distribution. The same holds for their entropy upon time-reversal. This behavior, as supported by numerical simulations in fBm time series and in
arxiv   +1 more source

Sudden cardiac death in inherited cardiomyopathy [PDF]

, 2017
Cardiomyopathy is an important cause of sudden cardiac death particularly in adolescents and young adults. The risk of sudden cardiac death varies between individual cardiomyopathies and is dependent on the severity of disease, age and gender.
Collis, R, Elliott, PM
core   +1 more source

Transthyretin amyloid cardiomyopathy: Literature review and red‐flag symptom clusters for each cardiology specialty

ESC Heart Failure, Volume 12, Issue 2, Page 955-967, April 2025.
Abstract Wild‐type transthyretin amyloid cardiomyopathy (ATTRwt‐CM) is a progressive and infiltrative cardiac disorder that may cause fatal consequences if left untreated. The estimated survival time from diagnosis is approximately 3–6 years. Because of the non‐specificity of initial symptom manifestation and insufficient awareness among treating ...
Yasuhiro Izumiya, Toru Kubo, Jin Endo, Seiji Takashio, Masatoshi Minamisawa, Jun Hamada, Tomonori Ishii, Hajime Abe, Hiroaki Konishi, Kenichi Tsujita   +9 more
wiley   +1 more source

Electrical Devices (Resynchronization and Defibrillators) in the Treatment of Cardiomyopathies: Indications, Present and Future of these Therapies [PDF]

, 2017
Cardiomyopathies are heart diseases involving high risk of heart failure and sudden cardiac death. In this chapter, we review the use of electrical devices (cardiac resynchronization therapy and implantable cardioverter defibrillator) to reduce the ...
Bertolo Domínguez, Marta, García García, Miguel Ángel, Martínez Cornejo, Alfonso, Miranda Gozalvo, Vicente, Rosero Arenas, María de los Ángeles   +4 more
core   +2 more sources