Results 21 to 30 of about 23,188 (240)

Case report: A 56-year-old woman presenting with torsades de pointes and cardiac arrest associated with levosimendan administration and underlying congenital long QT syndrome type 1. [PDF]

Heliyon
Zha F, Li X, Yin H, Huang D, Du Y, Zhou C.   +5 more
europepmc   +2 more sources

Hashimoto's thyroiditis and congenital long QT syndrome: a dangerous addition causing torsades-case report. [PDF]

Eur Heart J Case Rep
Acharya R, Sabesan V, Pandit D, Schuller D, Tripathi B.   +4 more
europepmc   +3 more sources

Repotrectinib in a Patient With <i>NTRK</i> Fusion-Positive Pancreatic Carcinoma and Congenital Long QT Syndrome. [PDF]

JCO Precis Oncol
Yun KM, Yun KM, Narezkina A, Redfern C, Velasco K, Bazhenova L.   +5 more
europepmc   +3 more sources

Induced Pluripotent Stem Cells in Congenital Long QT Syndrome: Research Progress and Clinical Applications. [PDF]

Rev Cardiovasc Med
Li Q, Wang YF, Wang B, Lv TT, Zhang P.
europepmc   +3 more sources

Cardiac Arrest Following Torsades de Pointes Caused by Hypokalemia and Catecholamines in a Patient with Congenital Long QT Syndrome Type 1 After Surgical Aortic Valve Replacement: A Case Report. [PDF]

Am J Case Rep, 2022
Kitaura A, Nakao S, Yuasa H, Tsukimoto S, Nakajima Y.   +4 more
europepmc   +2 more sources

Congenital long QT syndrome in children [PDF]

Medicinski Podmladak, 2016
Long QT syndrome (LQTS) is a cardiac repolarization disorder characterized by prolonged QT interval on the electrocardiogram (ECG) and increased propensity to ventricular tachyarrhythmias and cardiac events.
Cerović Ivana, Košutić Jovan
doaj   +1 more source

Clinical Advances in Congenital Long QT Syndrome

Cardiology Discovery, 2021
. Long QT syndrome is an inherited arrhythmia characterized by a prolonged QT interval and increased risk of life-threatening cardiac events, including arrhythmogenic syncope, seizures, and sudden cardiac death with a structurally normal heart. Since its
Kun Li, Ping Zhang, Xiaoxia Fu, Tianyu Xu.   +3 more
doaj   +1 more source

Sudden Cardiac Arrest in the Postpartum Period Due to Long QT Syndrome and Dilated Cardiomyopathy

JACC: Case Reports, 2023
We describe the case of a previously healthy patient presenting with sudden cardiac arrest in the postpartum period as a result of concomitant congenital type 1 long QT syndrome and BAG3 dilated cardiomyopathy.
Daniel R. Patterson, MD, Jonathan A. Pan, MD, Nisha Hosadurg, MBBS, Mohamed Morsy, MD   +3 more
doaj   +1 more source

Comparative Characteristics of Beta-Blockers in Patients with Congenital Long QT Syndrome

Рациональная фармакотерапия в кардиологии, 2021
Congenital long QT syndrome is a pathology that requires special attention and knowledge about the safety and effectiveness of various medications.
A. Yu. Proshlyakov, P. Sh. Chomakhidze, N. A. Novikova   +2 more
doaj   +1 more source

In Vitro Drug Screening Using iPSC-Derived Cardiomyocytes of a Long QT-Syndrome Patient Carrying KCNQ1 & TRPM4 Dual Mutation: An Experimental Personalized Treatment

Cells, 2022
Congenital long QT syndrome is a type of inherited cardiovascular disorder characterized by prolonged QT interval. Patient often suffer from syncopal episodes, electrocardiographic abnormalities and life-threatening arrhythmia.
Feifei Wang, Yafan Han, Wanyue Sang, Lu Wang, Xiaoyan Liang, Liang Wang, Qiang Xing, Yankai Guo, Jianghua Zhang, Ling Zhang, Tuerhong Zukela, Jiasuoer Xiaokereti, Yanmei Lu, Xianhui Zhou, Baopeng Tang, Yaodong Li   +15 more
doaj   +1 more source