Brugada syndrome is an inherited cardiac channelopathy arising from mutations in voltage-
gated cardiac sodium channels. Idiopathic epilepsy portrays a coalescent underlying …

Abstract Penyakit Paru Obstruksi Kronik (PPOK) adalah penyakit yang umum, dapat dicegah
dan diobati, ditandai dengan gejala pernapasan persisten dan keterbatasan aliran udara …

Abstract Background Brugada syndrome (BrS) is a primary electrical disease associated
with an increased risk of sudden cardiac death due to ventricular fibrillation. This pathology …

Calcium/calmodulin-dependent protein kinase II (CaMKII) regulates the principle ion
channels mediating cardiac excitability and conduction, but how this regulation translates to …

The “stress” kinases cAMP-dependent protein kinase (PKA) and calcium/calmodulin-
dependent protein kinase II (CaMKII), phosphorylate the Na+ channel Nav1. 5 subunit to …

Abstract Plakophilin‐2 (PKP 2) variants could produce a phenotype of Brugada syndrome
(BrS), which seems to be most likely the same allelic disorder as some sudden unexplained …

The n-3 polyunsaturated fatty acids (PUFAs), including eicosapentaenoic acid (EPA) and
docosahexaenoic acid (DHA), have antiarrhythmic effects, possibly via modulation of the …

The Brugada syndrome is an inherited channelopathy that alters the main transmembrane
ion currents that constitute the cardiac action potential. These changes not only modify the …

Background: Sudden death of a newborn is a rare entity, which may be caused by genetic
cardiac arrhythmias. Among these diseases, Long QT syndrome is the most prevalent …

Background: Brugada syndrome (BrS) is a rare inherited cardiac arrhythmia with increased
risk of sudden cardiac death. Mutations in gene SCN5A, which encodes the α-subunit of …