These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
303 related articles for article (PubMed ID: 23837003)
1. Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies. Hsiao PY; Tien HC; Lo CP; Juang JM; Wang YH; Sung RJ Appl Clin Genet; 2013; 6():1-13. PubMed ID: 23837003 [TBL] [Abstract][Full Text] [Related]
2. Role of pharmacotherapy in cardiac ion channelopathies. El-Sherif N; Boutjdir M Pharmacol Ther; 2015 Nov; 155():132-42. PubMed ID: 26376080 [TBL] [Abstract][Full Text] [Related]
3. Modeling genetic cardiac channelopathies using induced pluripotent stem cells - Status quo from an electrophysiological perspective. Kamga MVK; Reppel M; Hescheler J; Nguemo F Biochem Pharmacol; 2021 Oct; 192():114746. PubMed ID: 34461117 [TBL] [Abstract][Full Text] [Related]
4. Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. Kaufman ES Heart Rhythm; 2009 Aug; 6(8 Suppl):S51-5. PubMed ID: 19631908 [TBL] [Abstract][Full Text] [Related]
5. Role of pharmacotherapy in cardiac ion channelopathies. El-Sherif N; Pedalino R; Himel H Curr Vasc Pharmacol; 2009 Jul; 7(3):358-66. PubMed ID: 19601860 [TBL] [Abstract][Full Text] [Related]
6. Arrhythmogenic hereditary syndromes: Brugada Syndrome, long QT syndrome, short QT syndrome and CPVT. Schimpf R; Veltmann C; Wolpert C; Borggrefe M Minerva Cardioangiol; 2010 Dec; 58(6):623-36. PubMed ID: 21135804 [TBL] [Abstract][Full Text] [Related]
13. Surgical cardiac denervation therapy for treatment of congenital ion channelopathies in pediatric patients: a contemporary, single institutional experience. Costello JP; Wilson JK; Louis C; Peer SM; Zurakowski D; Nadler EP; Qureshi FG; Jonas RA; Greene EA; Berul CI; Moak JP; Nath DS World J Pediatr Congenit Heart Surg; 2015 Jan; 6(1):33-8. PubMed ID: 25548341 [TBL] [Abstract][Full Text] [Related]
14. Ion Channel Disorders and Sudden Cardiac Death. Garcia-Elias A; Benito B Int J Mol Sci; 2018 Feb; 19(3):. PubMed ID: 29495624 [TBL] [Abstract][Full Text] [Related]
15. Recent understanding of clinical sequencing and gene-based risk stratification in inherited primary arrhythmia syndrome. Aiba T J Cardiol; 2019 May; 73(5):335-342. PubMed ID: 30910390 [TBL] [Abstract][Full Text] [Related]
16. Genetics of congenital long QT syndrome and Brugada syndrome. Shimizu W Future Cardiol; 2008 Jul; 4(4):379-89. PubMed ID: 19804318 [TBL] [Abstract][Full Text] [Related]
17. Avoiding sports-related sudden cardiac death in children with congenital channelopathy : Recommendations for sports activities. Lang CN; Steinfurt J; Odening KE Herz; 2017 Apr; 42(2):162-170. PubMed ID: 28233036 [TBL] [Abstract][Full Text] [Related]
19. Pharmacological approach to the treatment of long and short QT syndromes. Patel C; Antzelevitch C Pharmacol Ther; 2008 Apr; 118(1):138-51. PubMed ID: 18378319 [TBL] [Abstract][Full Text] [Related]
20. Inherited calcium channelopathies in the pathophysiology of arrhythmias. Venetucci L; Denegri M; Napolitano C; Priori SG Nat Rev Cardiol; 2012 Oct; 9(10):561-75. PubMed ID: 22733215 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]