Cargando…
Brugada syndrome
A novel clinical entity characterized by ST segment elevation in right precordial leads (V1 to V3), incomplete or complete right bundle branch block, and susceptibility to ventricular tachyarrhythmia and sudden cardiac death has been described by Brugada et al. in 1992. This disease is now frequentl...
Autores principales: | Napolitano, Carlo, Priori, Silvia G |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592481/ https://www.ncbi.nlm.nih.gov/pubmed/16972995 http://dx.doi.org/10.1186/1750-1172-1-35 |
Ejemplares similares
-
Brugada Syndrome: Oligogenic or Mendelian Disease?
por: Monasky, Michelle M., et al.
Publicado: (2020) -
Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome
por: Di Mauro, Vittoria, et al.
Publicado: (2021) -
Genetics of Brugada syndrome
por: Juang, Jyh-Ming Jimmy, et al.
Publicado: (2016) -
Not All Brugada Electrocardiogram Patterns are Brugada Syndrome or Brugada Phenocopy
por: Xu, Grace, et al.
Publicado: (2017) -
Impact of Dietary Factors on Brugada Syndrome and Long QT Syndrome
por: D’Imperio, Sara, et al.
Publicado: (2021)