Congenital long QT syndrome: Pathophysiology and genetics

AR Rebelo, A Lopes, C Magalhães, J Sarmento… - Revista Portuguesa de …, 2021 - rpmgf.pt

Introdução: A síncope é um motivo frequente de preocupação em idade pediátrica. Apesar
da sua etiologia ser maioritariamente benigna, é essencial excluir causas graves e …

被引用次数：1 相关文章所有 2 个版本

[PDF] unige.ch

[PDF][PDF] Evaluation et systématisation des pratiques de prescription médicamenteuse chez les adultes avec déficience intellectuelle

J Desmeules, PM Besson, DM Kosel - access.archive-ouverte.unige.ch

Historiquement, la terminologie de la déficience intellectuelle (DI) a beaucoup varié avec
des termes tels que l'idiotie, l'imbécillité et la faiblesse d'esprit. Dans les années 1960, ces …

[PDF] mcgill.ca

[图书][B] Heteromeric interactions between wild-type and mutant subunits of the ether-a-go-go related gene (hERG) channel, in the context of the type II congenital Long …

T Wang - 2020 - search.proquest.com

Mutations in the human Ether-a-go-go-Related Gene (hERG1, or KCNH2) are linked to the
type 2 congenital Long QT syndrome (LQT2), characterized by delayed ventricular …

Surgical Approach in Congenital Long QT Interval Syndrome Patients

D Stoldere, E Cimbolineca - Acta Chirurgica Latviensis, 2020 - sciendo.com

Long QT syndrome is a genetically determined clinical condition that can lead to sudden
cardiac death, life–threatening arrhythmias, typically ventricular tachycardia–Torsades de …

[PDF][PDF] Vrodený syndróm dlhého QT intervalu

MUDJ Tomko, MUDM Bjeloševič, MUDM Chalupka… - solen.sk

Vrodený syndróm dlhého QT intervalu (z angl. long QT syndrome–LQTS) je najčastejšie sa
vyskytujúcim primárnym kardiálnym arytmickým syndrómom. Ochorenie sa typicky prejavuje …