Congenital short QT syndrome: Landmarks of the newest arrhythmogenic cardiac channelopathy

ARP Riera, A Paixão-Almeida… - Cardiology …, 2013 - journals.viamedica.pl
Congenital or familial short QT syndrome is a genetically heterogeneous cardiac
channelopathy without structural heart disease that has a dominant autosomal or sporadic …

Different sensitivity to the suppressive effects of isoflurane anesthesia on cardiorespiratory function in SHR/Izm, WKY/Izm, and Crl: CD (SD) rats

K Kato, J Wakai, K Ozawa, M Sekiguchi… - Experimental …, 2016 - jstage.jst.go.jp
Isoflurane is a widely used anesthetic, but its effects with increase in inspired concentration
on cardiovascular function have not yet been clarified in rodents. Additionally, there are only …

遗传性心律失常的体表心电图线索.

史炳硕, 李广平 - Journal of Practical Electrocardiology, 2022 - search.ebscohost.com
遗传性心律失常(inherited arrhythmia, IA) 是一类以各种心律失常发作为主要特征的遗传性疾病
的统称, 主要包括遗传性离子通道病和遗传性结构性心脏病. IA 猝死风险很高 …

[PDF][PDF] Short QT syndrome and idiopathic ventricular tachycardia in a 28-year-old young man: a potential disease-specific link?

S Sadeghian, A Bozorgi, Z Safkhani - Europace, 2014 - escardio.org
A 28-year-old man was admitted to the Emergency Department because of palpitations. 1
He suffered from paroxysmal palpitation episodes during exercise, especially while …

Supawat Ratanapo, MD

QT Short - Cleveland Clinic Journal of Medicine - mdedge9-ma1.mdedge.com
To the Editor: We read with great interest the article by Drs. Al Maluli and Meshkov on short
QT syndrome in the January 2013 issue. 1 We are wondering whether Holter monitoring and …

Non-invasive detection of hyperglycaemia in type 1 diabetic patients using electrocardiographic signals

LL Nguyen - 2014 - opus.lib.uts.edu.au
Hyperglycaemia is the medical term for a state caused by a high level of blood glucose,
resulting from defects in insulin secretion, insulin action, or both. Hyperglycaemia is a …

[PDF][PDF] TÜRK TOPLUMUNDA 5-40 YAŞ ARASI ANİ ÖLÜMLERİN GENOM BOYU KARDİYOVASKÜLER HASTALIK RİSK

DRO ÖZTÜRK, GÖ CAVLAK - nek.istanbul.edu.tr
Doktora eğitim süresi boyunca bana her türlü desteği veren, hep yanımda ve yardımcı olan
sevgili hocam Prof. Dr. Oğuz ÖZTÜRK'e, ayrıca eğitimim boyunca işlerimi kolaylaştıran sayın …

[HTML][HTML] The Pharmacogenomics of a Mutation “Hotspot” for the Short QT Syndrome

D Darbar, MD McCauley - JACC: Clinical Electrophysiology, 2017 - jacc.org
Short QT syndrome (SQTS) is a recently described genetic cardiac ion channelopathy that
predisposes patients to atrial arrhythmia, ventricular arrhythmia, and sudden cardiac death …

Genomic-based diagnosis of arrhythmia disease in a personalized medicine era

A Omar, M Zhou, A Berman, RA Sorrentino… - Expert review of …, 2016 - Taylor & Francis
Introduction: Although thousands of potentially disease-causing mutations have been
identified in a handful of genes, the genetic heterogeneity has led to diagnostic confusions …

Etiology of cardiac arrest in the absence of manifest structural heart disease: update from the CASPER prospective cohort.

A Herman - 2015 - open.library.ubc.ca
Background: The Cardiac Arrest Survivors with Preserved Ejection Fraction Registry
(CASPER) enrolls patients with apparently unexplained cardiac arrest and no evident …