Cargando…
Cardiac Sodium Channel Dysfunction and Dilated Cardiomyopathy: A Contemporary Reappraisal of Pathophysiological Concepts
A key emerging theme in translational cardiovascular medicine is the need to identify specific causes of arrhythmias and heart failure, defined by phenotype and/or genotype that will respond to a particular intervention. Unlike other genes implicated in hereditary arrhythmias and cardiomyopathies, p...
Autor principal: | Asatryan, Babken |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678327/ https://www.ncbi.nlm.nih.gov/pubmed/31336969 http://dx.doi.org/10.3390/jcm8071029 |
Ejemplares similares
-
Enhancing risk stratification for life‐threatening ventricular arrhythmias in dilated cardiomyopathy: the peril and promise of precision medicine
por: Asatryan, Babken, et al.
Publicado: (2020) -
The Ever-Expanding Landscape of Cardiomyopathies
por: Asatryan, Babken, et al.
Publicado: (2020) -
Sex-related differences in incidence, phenotype and risk of sudden cardiac death in inherited arrhythmia syndromes
por: Asatryan, Babken, et al.
Publicado: (2023) -
A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy
por: Moreau, Adrien, et al.
Publicado: (2018) -
Interleukin-1 in cardiac injury, repair, and remodeling: pathophysiologic and translational concepts
por: Frangogiannis, Nikolaos G.
Publicado: (2015)