Results 161 to 170 of about 37,848 (274)
Aim To evaluate the efficacy and safety of oral zuranolone for 14 days, compared with placebo, in Japanese patients with major depressive disorder (MDD). Methods This multicenter, Phase 3 study was conducted in two parts (70 sites; Japan) including a randomized, double‐blind, placebo‐controlled, parallel‐group part presented herein.
Masaki Kato +8 more
wiley +1 more source
Inhibitory effect of oestradiol on the cardiac KV7.1/KCNE1 channel is species dependent
Abstract Oestradiol (17β‐E2) is reported to prolong the cardiac action potential duration and QT interval, in part by affecting cardiac ion channels. Previous studies found inhibiting 17β‐E2 effects on the repolarizating cardiac KV7.1/KCNE1 channel, or its native current, in heterologous expression systems or tissue from animal species.
Veronika A. Linhart +2 more
wiley +1 more source
Holter Monitor QT Dispersion and QTc-Dispersion in Pediatric Long QT Syndrome and Development of a Diagnostic and Arrhythmia Risk Prediction Model. [PDF]
Allam H +8 more
europepmc +1 more source
Niacin (vitamin B3) is involved in the metabolic regulation of energy metabolism in animals. However, both deficiency and excess supplementation of niacin can induce profound physiological disturbances in fish. The present study investigated the effect of niacin on energy metabolism and liver health in Nile tilapia (Oreochromis niloticus).
Ruixin Li +11 more
wiley +1 more source
Congenital Long QT Syndrome: A Focus on Risk Stratification and Management. [PDF]
Ranganathan D +3 more
europepmc +1 more source
Congenital complete atrioventricular block (CAVB) is a rare cardiac condition occurring in approximately one in 15,000 to one in 22,000 live births. Maternal autoimmune diseases, with anti‐ssA (Ro) and anti‐ssB (La) antibodies implicated in 56%–90% of cases, are primary causes.
Ferrari Paola +5 more
wiley +1 more source
Perioperative management of thoracoscopic left cardiac sympathetic denervation for refractory long QT syndrome: a case report. [PDF]
Nitta A +7 more
europepmc +1 more source
A Common Mutation of Long QT Syndrome Type 1 in Japan
Hideki Itoh +12 more
openalex +2 more sources
Identification of Two Rare Variants in Iranian Families With Familial Sudden Cardiac Death
Cellular action potential is characterized by a particular sequence of depolarizing and repolarizing ion currents regulated by ion channels. Genetic mutations in these channels disrupt the essential movement of ions, such as Na+, Ca++, and K+, across the cell membrane, leading to dangerous arrhythmias and sudden cardiac death (SCD).
Mahsa Tahmasebivand +10 more
wiley +1 more source
Postpartum QT Prolongation in a Long QT Syndrome Type 1 Patient. [PDF]
Wiedenmann LC, Ehrlich JR, Goldenberg I.
europepmc +1 more source

