Results 21 to 30 of about 8,451,399 (181)
Hepatology, EarlyView., 2022 Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel +93 more
wiley +1 more source
Case report of antiseizure medicine-induced long QT syndrome and a literature review
Acta Epileptologica, 2022 Background To realize the clinical characteristics of long QT syndrome (LQTS) caused by antiseizure medicines (ASMs), and to improve the prevention and management of ASM-acquired QT syndrome.
Xiongying Yu +6 more
doaj +1 more source
Long QT in stunned myocardium: unrecognised cause of acquired long QT syndrome
Journal of Medical Science, 2014 Long QT syndrome (LQTS) is a heart disorder characterized by a prolongation of the QT interval on ECG and a predisposition to ventricular tachyarrhythmias, which may lead to syncope, cardiac arrest or sudden cardiac death. This condition may be inherited
Jerzy Sacha
doaj +1 more source
Paediatric/young versus adult patients with long QT syndrome [PDF]
, 2021 Introduction Long QT syndrome (LQTS) is a less prevalent cardiac ion channelopathy than Brugada syndrome in Asia. The present study compared the outcomes between paediatric/young and adult LQTS patients. Methods This was a population-based retrospective
Gary Tse +9 more
core +1 more source
Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome [PDF]
, 2011 The short QT syndrome (SQTS) is a genetically heterogeneous condition characterized by abbreviated QT intervals and an increased susceptibility to arrhythmia and sudden death.
Hancox Jules C. +24 more
core +2 more sources
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 +2 more
doaj +1 more source
Acquired long QT syndrome and Torsades de Poin
The Egyptian Heart Journal, 2016 Acetylcholinesterase inhibitors are group of drugs commonly used in Alzheimer disease and have beneficial effects on treatment. Although they have many known side effects, cardiovascular side effects are rarely seen.
Ahmet Seyfeddin Gurbuz +7 more
doaj +1 more source
Utility of Zebrafish Models of Acquired and Inherited Long QT Syndrome
Frontiers in Physiology, 2021 Long-QT Syndrome (LQTS) is a cardiac electrical disorder, distinguished by irregular heart rates and sudden death. Accounting for ∼40% of cases, LQTS Type 2 (LQTS2), is caused by defects in the Kv11.1 (hERG) potassium channel that is critical for cardiac
Kyle E. Simpson +6 more
doaj +1 more source
Torsades de pointes in the PACU after outpatient endoscopy: a case report
BMC Anesthesiology, 2021 Background This case demonstrates the severe electrolyte derangements that may present after a common therapy such as a bowel preparation for an outpatient procedure and the rare yet potential detrimental outcomes of those abnormalities.
Andrew Schaar +2 more
doaj +1 more source
Transient Long QT Development in a Patient with Takotsubo Cardiomyopathy
Journal of Cardiovascular Emergencies, 2016 QT interval prolongation on the electrocardiogram is considered a precursory sign for imminent, potentially lethal ventricular arrhythmias. Beside the inherited condition of long QT syndrome, numerous drugs, certain electrolyte disturbances and early ...
Czuriga Dániel +10 more
doaj +1 more source