Results 31 to 40 of about 29,179 (198)

Can wearables outscore general practitioners? Congenital long QT syndrome diagnosis initiated by a smartwatch. [PDF]

HeartRhythm Case Rep
Rudic B, Kauferstein S, Akin I, Borggrefe M.   +3 more
europepmc   +2 more sources

Effectiveness and Limitations of β-Blocker Therapy in Congenital Long-QT Syndrome [PDF]

Circulation, 2001
Robert M. Gow
openalex   +2 more sources

Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT Syndrome. [PDF]

JACC Clin Electrophysiol, 2020
Moore JP, Gallotti RG, Shannon KM, Bos JM, Sadeghi E, Strasburger JF, Wakai RT, Horigome H, Clur SA, Hill AC, Shah MJ, Behere S, Sarquella-Brugada G, Czosek R, Etheridge SP, Fischbach P, Kannankeril PJ, Motonaga K, Landstrom AP, Williams M, Patel A, Dagradi F, Tan RB, Stephenson E, Krishna MR, Miyake CY, Lee ME, Sanatani S, Balaji S, Young ML, Siddiqui S, Schwartz PJ, Shivkumar K, Ackerman MJ.   +33 more
europepmc   +2 more sources

Vortioxetine Can Be Used Safely to Treat Depression After Implantable Cardioverter Defibrillator Implantation for Congenital Long QT Syndrome: A Case Report. [PDF]

Neuropsychopharmacol Rep
Yamauchi M, Otsuki K, Sato K, Nagahama M, Tanabe J, Inagaki M.   +5 more
europepmc   +3 more sources

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

Circulation, 2020
Supplemental Digital Content is available in the text. Background: Long QT syndrome (LQTS) is the first described and most common inherited arrhythmia.
A. Adler, V. Novelli, A. Amin, E. Abiusi, M. Care, E. Nannenberg, H. Feilotter, S. Amenta, D. Mazzà, H. Bikker, A. Sturm, John Garcia, M. Ackerman, R. E. Hershberger, M. Perez, W. Zareba, J. Ware, A. Wilde, M. Gollob   +18 more
semanticscholar   +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

GENETIC ASPECTS OF CONGENITAL LONG QT SYNDROME

Рациональная фармакотерапия в кардиологии, 2015
The main symptoms and clinical types of long QT syndrome are described. Molecular genetic diagnostics and updated approaches to the management of patients with long QT syndrome arepresented.
A. A. Chernova, S. Yu. Nikulina, A. V. Gul'bis   +2 more
doaj   +3 more sources

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

Resuscitation of sudden cardiac death caused by acute epileptic seizures: A case report

Journal of Acute Disease, 2016
Symptomatic long QT syndrome in pediatric patients is a life-threatening condition. Sometimes, this pathology can be misdiagnosed and erroneously managed as generalized epilepsy due to similar clinical manifestations.
Dana-Oliviana Geavlete, Oana Ionita, Leonard Mandes, Iulia Kulcsar, Emanuel Stoica, Radu Ciudin, Cezar Macarie, Ovidiu Chioncel   +7 more
doaj   +1 more source