Cargando…
Ion Channel Disorders and Sudden Cardiac Death
Long QT syndrome, short QT syndrome, Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia are inherited primary electrical disorders that predispose to sudden cardiac death in the absence of structural heart disease. Also known as cardiac channelopathies, primary electrical dis...
Autores principales: | Garcia-Elias, Anna, Benito, Begoña |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877553/ https://www.ncbi.nlm.nih.gov/pubmed/29495624 http://dx.doi.org/10.3390/ijms19030692 |
Ejemplares similares
-
Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease
por: Martin, Claire A, et al.
Publicado: (2012) -
Cardiac Ion Channelopathies and the Sudden Infant Death Syndrome
por: Wilders, Ronald
Publicado: (2012) -
Autoantibodies for Cardiac Channels and Sudden Cardiac Death and its Relationship to Autoimmune Disorders
por: Chera, Hymie, et al.
Publicado: (2019) -
Sudden Cardiac Death
por: Weinberg, Marc
Publicado: (1978) -
Ion Channel Remodeling—A Potential Mechanism Linking Sleep Apnea and Sudden Cardiac Death
por: Chahal, Anwar Ahmed, et al.
Publicado: (2016)