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Page 1
Inherited cardiac arrhythmias.
Schwartz PJ, Ackerman MJ, Antzelevitch C, Bezzina CR, Borggrefe M, Cuneo BF, Wilde AAM. Schwartz PJ, et al. Nat Rev Dis Primers. 2020 Jul 16;6(1):58. doi: 10.1038/s41572-020-0188-7. Nat Rev Dis Primers. 2020. PMID: 32678103 Free PMC article. Review.
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia and Brugada syndrome. ...Future research should focus on the identification of genes associated with the …
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymor …
Latent Causes of Sudden Cardiac Arrest.
Krahn AD, Tfelt-Hansen J, Tadros R, Steinberg C, Semsarian C, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 Jun;8(6):806-821. doi: 10.1016/j.jacep.2021.12.014. JACC Clin Electrophysiol. 2022. PMID: 35738861 Free article. Review.
Inherited arrhythmia syndromes are a common cause of apparently unexplained cardiac arrest or sudden cardiac death. These include long QT syndrome and Brugada syndrome, with a well-recognized phenotype in most patients with sufficiently severe disease …
Inherited arrhythmia syndromes are a common cause of apparently unexplained cardiac arrest or sudden cardiac death. These include long …
Role of the autonomic nervous system in modulating cardiac arrhythmias.
Shen MJ, Zipes DP. Shen MJ, et al. Circ Res. 2014 Mar 14;114(6):1004-21. doi: 10.1161/CIRCRESAHA.113.302549. Circ Res. 2014. PMID: 24625726 Review.
Neural modulation as a treatment for arrhythmias has been well established in certain diseases, such as long QT syndrome. However, in most other arrhythmia diseases, it is still an emerging modality and under investigation. ...
Neural modulation as a treatment for arrhythmias has been well established in certain diseases, such as long QT syndrome …
Risk factors for QTc-prolongation: systematic review of the evidence.
Vandael E, Vandenberk B, Vandenberghe J, Willems R, Foulon V. Vandael E, et al. Int J Clin Pharm. 2017 Feb;39(1):16-25. doi: 10.1007/s11096-016-0414-2. Epub 2016 Dec 23. Int J Clin Pharm. 2017. PMID: 28012118 Review.
Results Ten observational studies could be included, with a total of 89,532 patients [prospective cohort design: N = 6; multiple regression analyses: N = 5; median STROBE score = 17/22 (range 15-18)]. ...
Results Ten observational studies could be included, with a total of 89,532 patients [prospective cohort design: N = 6; multiple regr …
The Lancet Commission to reduce the global burden of sudden cardiac death: a call for multidisciplinary action.
Marijon E, Narayanan K, Smith K, Barra S, Basso C, Blom MT, Crotti L, D'Avila A, Deo R, Dumas F, Dzudie A, Farrugia A, Greeley K, Hindricks G, Hua W, Ingles J, Iwami T, Junttila J, Koster RW, Le Polain De Waroux JB, Olasveengen TM, Ong MEH, Papadakis M, Sasson C, Shin SD, Tse HF, Tseng Z, Van Der Werf C, Folke F, Albert CM, Winkel BG. Marijon E, et al. Lancet. 2023 Sep 9;402(10405):883-936. doi: 10.1016/S0140-6736(23)00875-9. Epub 2023 Aug 27. Lancet. 2023. PMID: 37647926 Review.
Medical Therapy for Long QT Syndrome.
Adamos G, Iacovidou N, Xanthos T. Adamos G, et al. Mini Rev Med Chem. 2018;18(6):495-506. doi: 10.2174/1389557517666170707110000. Mini Rev Med Chem. 2018. PMID: 28685698 Review.
Long QT syndrome (LQTS) is an arrhythmogenic disorder characterized by repolarization abnormalities with a tendency to cause life threatening cardiac events. ...Both pharmacological and interventional therapies (left cardiac sympathetic denervation, ICDs) hav …
Long QT syndrome (LQTS) is an arrhythmogenic disorder characterized by repolarization abnormalities with a tendency to …
Congenital Long QT syndrome and torsade de pointes.
El-Sherif N, Turitto G, Boutjdir M. El-Sherif N, et al. Ann Noninvasive Electrocardiol. 2017 Nov;22(6):e12481. doi: 10.1111/anec.12481. Epub 2017 Jul 2. Ann Noninvasive Electrocardiol. 2017. PMID: 28670758 Free PMC article. Review.
Since its initial description by Jervell and Lange-Nielsen in 1957, the congenital long QT syndrome (LQTS) has been the most investigated cardiac ion channelopathy. A prolonged QT interval in the surface electrocardiogram is the sine qua non of the LQT …
Since its initial description by Jervell and Lange-Nielsen in 1957, the congenital long QT syndrome (LQTS) has been the …
Potassium channelopathies.
Sanguinetti MC, Spector PS. Sanguinetti MC, et al. Neuropharmacology. 1997 Jun;36(6):755-62. doi: 10.1016/s0028-3908(97)00029-4. Neuropharmacology. 1997. PMID: 9225302 Review.
These include the human disorders of episodic ataxia with myokymia, long QT syndrome and Bartter's syndrome, and weaver ataxia in mice. ...
These include the human disorders of episodic ataxia with myokymia, long QT syndrome and Bartter's syndrome, and …
Evaluation and Management of Athletes With Long QT Syndrome.
Gomez AT, Prutkin JM, Rao AL. Gomez AT, et al. Sports Health. 2016 Nov/Dec;8(6):527-535. doi: 10.1177/1941738116660294. Epub 2016 Aug 6. Sports Health. 2016. PMID: 27480102 Free PMC article. Review.
CONTEXT: The congenital long QT syndrome (LQTS) is an inherited channelopathy known for its electrocardiographic manifestations of QT prolongation and its hallmark arrhythmia, torsades de pointes (TdP). ...EVIDENCE ACQUISITION: The following keywords w …
CONTEXT: The congenital long QT syndrome (LQTS) is an inherited channelopathy known for its electrocardiographic manife …
The diagnostic role of T wave morphology biomarkers in congenital and acquired long QT syndrome: A systematic review.
Tardo DT, Peck M, Subbiah RN, Vandenberg JI, Hill AP. Tardo DT, et al. Ann Noninvasive Electrocardiol. 2023 Jan;28(1):e13015. doi: 10.1111/anec.13015. Epub 2022 Nov 7. Ann Noninvasive Electrocardiol. 2023. PMID: 36345173 Free PMC article. Review.
INTRODUCTION: QTc prolongation is key in diagnosing long QT syndrome (LQTS), however 25%-50% with congenital LQTS (cLQTS) demonstrate a normal resting QTc. ...METHODS: Electronic databases were searched using the terms "LQTS," "long QT syndro …
INTRODUCTION: QTc prolongation is key in diagnosing long QT syndrome (LQTS), however 25%-50% with congenital LQTS (cLQT …
249 results