Results 111 to 120 of about 2,626,293 (190)
Arrhythmogenic right ventricular cardiomyopathy, a genetically inherited disease that results in fibrofatty replacement of normal cardiac myocytes, has been associated with sudden cardiac death in athletes.
Ibhar Al Mheid +4 more
core +1 more source
BackgroundArrhythmogenic right ventricular cardiomyopathy (ARVC) is most commonly associated with pathogenic variants in desmosomal genes. However, ARVC-like phenotypes may also arise from non-desmosomal genetic backgrounds, creating diagnostic ...
Bo Eun Park +3 more
doaj +1 more source
In NHANES III adults, latent class trajectory analysis identified a J‐point phenotype characterized by higher V4 amplitude and a steep decline toward V6. This spatial trajectory was independently associated with increased long‐term all‐cause mortality and cardiac death, suggesting prognostic value beyond conventional early repolarization criteria ...
Chenhui Tai, Zhe Wang
wiley +1 more source
Arrhythmogenic right ventricular cardiomyopathy with sinus node dysfunction
Introduction: The 2023 European Society of Cardiology Guidelines for the management of Cardiomyopathies recommends a phenotype-based, multimodal, multidisciplinary, and multiparametric approach to the diagnosis of cardiomyopathies.
Bánfi-Bacsárdi Fanni +10 more
core +1 more source
The V6R/V4R amplitude index is a novel and practical electrocardiographic parameter for identifying idiopathic ventricular arrhythmias originating from the aortic cusp. A cutoff >0.55 accurately distinguishes cusp from adjacent non‐cusp origins within the left ventricular outflow tract, facilitating targeted mapping and procedural planning.
Yoshihisa Naruse +19 more
wiley +1 more source
Patient selection and analysis flow diagram. The exact pre‐inclusion denominator and reliable reason‐specific exclusion counts could not be reconstructed because a prospectively maintained screening log was unavailable. The diagram summarizes the final study cohort and analysis‐specific sample sizes. AF, atrial fibrillation; LVA, low‐voltage area; SR1,
Yunus Emre Özbebek +7 more
wiley +1 more source
Arrhythmogenic right ventricular cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a familial form of cardiomyopathy predominantly affecting the right ventricle but may progress to involve the left ventricle as well. At the late stage of the disease, it is sometimes difficult to
John E Sanderson +5 more
core +1 more source
ABSTRACT Background In patients with structural heart disease (SHD) and moderately impaired left ventricular ejection fraction (LVEF > 35%), data on outcomes after ventricular tachycardia (VT) ablation remain limited. This analysis focuses on VT recurrence after ablation in patients presenting with sustained VT and LVEF > 35% within a secondary ...
Said‐Elias Waezsada +14 more
wiley +1 more source
Arrhythmogenic Right Ventricular Cardiomyopathy Diagnosed with 2020 International Criteria
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare cardiomyopathy. Early diagnosis is important to prevent mortality. They have a high risk of sudden cardiac death due to ventricular arrhythmia, which requires the implantation of a ...
Neelesh Damor +4 more
doaj +1 more source
ABSTRACT This current study aimed to decipher the anti‐inflammatory, anti‐ferroptosis and pronounced lung‐protective activities of Salvianolic acid B (Sal B) by integrating network pharmacology and experimental confirmation across multiple aspects. The optimal target protein and the relevant molecular mechanisms for Sal B in the context of ALI were ...
Hejun Gao +4 more
wiley +1 more source

