Results 131 to 140 of about 23,188 (240)

Genetics of inherited primary arrhythmia disorders

The Application of Clinical Genetics, 2015
Danna A Spears, Michael H Gollob Division of Cardiology – Electrophysiology, University Health Network, Toronto General Hospital, Toronto, ON, Canada Abstract: A sudden unexplained death is felt to be due to a primary arrhythmic disorder when no ...
Spears DA, Gollob MH
doaj  

Fetal Tachyarrhythmia - Part I: Diagnosis [PDF]

, 2004
Fetal tachycardia, first recognized in 1930 by Hyman et al1, is a condition occurring in approximately 0.4-0.6% of all pregnancies2. A subset of these cases with more sustained periods of tachycardia is clinically relevant.
Meijboom, Erik J, Oudijk, Martijn A, Visser, Gerard HA   +2 more
core   +3 more sources

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? [PDF]

, 2006
Nynke Hofman, A. A. M. Wilde, Stefan Kääb, Irene M. van Langen, Michael W.T. Tanck, Marcel M. A. M. Mannens, Martin Hinterseer, Britt Maria Beckmann, Hanno L. Tan   +8 more
openalex   +1 more source

Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long-QT Syndrome. [PDF]

J Am Heart Assoc, 2023
Vink AS, Hermans BJM, Hooglugt JQ, Peltenburg PJ, Meijborg VMF, Hofman N, Clur SB, Blom NA, Delhaas T, Wilde AAM, Postema PG.   +10 more
europepmc   +1 more source

Roles and regulation of the cardiac sodium channel Nav1.5: Recent insights from experimental studies [PDF]

, 2017
During the past decade, Nav1.5, the main voltage-gated Na+ channel in the heart, has been shown to be involved in many cardiac diseases. Genetic variants in the gene SCN5A, encoding Nav1.5, have been linked to various cardiac phenotypes, such as the ...
Abriel, Hugues
core  

Deep learning analysis of drug-induced ECG changes to inform arrhythmia risk and improve diagnosis of congenital long QT syndrome [PDF]

, 2021
Edi Prifti, Ahmad Fall, Giovanni Davogustto, Alfredo Pulini, Isabelle Denjoy, Christian Funck‐Brentano, Yasmin Khan, Alexandre Durand-Salmon, Quinn S. Wells, Antoine Leenhardt, Jean‐Daniel Zucker, Dan M. Roden, Fabrice Extramiana, Joe‐Elie Salem   +13 more
openalex   +1 more source

Low Baseline Fetal Heart Rate Leads to Diagnosis of Long QT Syndrome Type 1

JACC: Case Reports
A low baseline fetal heart rate at 20 weeks’ gestation was detected in a fetus without cardiac structural anomalies. Fetal echocardiography and magnetocardiography were used to diagnose congenital long QT syndrome.
Aleksandra Polic, MD, Stacy A.S. Killen, MD, MSCI, Janette F. Strasburger, MD, Prince J. Kannankeril, MD, MSCI, Ronald T. Wakai, PhD, Soha S. Patel, MD, MSPH   +5 more
doaj   +1 more source

Pueraria mirifica, an estrogenic tropical herb, unveiled the severity of Type 1 LQTS caused by KCNQ1‐T587M

Journal of Arrhythmia, 2021
Asami Kashiwa, Yukio Hosaka, Kazuyoshi Takahashi, Seiko Ohno, Yuko Wada, Takeru Makiyama, Hirotaka Oda, Minoru Horie   +7 more
doaj   +1 more source

Recent Advances in Congenital Long QT Syndrome [PDF]

, 2016
Shankar Baskar
openalex   +1 more source

Biological Life-Stage and the Burden of Cardiac Events in Women With Congenital Long QT Syndrome. [PDF]

Circ Arrhythm Electrophysiol, 2022
Younis A, Zareba W, Goldenberg I, Kharsa A, McNitt S, Aktas MK, Bodurian C, Farooq S, Polonsky B, Sotoodehnia N, Kudenchuk PJ, Rea TD, Arking DE, Luigi Bragazzi N, Goldenberg I.   +14 more
europepmc   +1 more source