Sex and Genotype in Long QT Syndrome Risk Stratification
- PMID: 30758500
- DOI: 10.1001/jamacardio.2018.4947
Sex and Genotype in Long QT Syndrome Risk Stratification
Comment on
-
Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients.JAMA Cardiol. 2019 Mar 1;4(3):246-254. doi: 10.1001/jamacardio.2018.4925. JAMA Cardiol. 2019. Retraction in: JAMA Cardiol. 2021 Jun 1;6(6):727. doi: 10.1001/jamacardio.2021.1087 PMID: 30758498 Free PMC article. Retracted.
Similar articles
-
Current perspectives on congenital long QT syndrome.Anadolu Kardiyol Derg. 2009 Dec;9 Suppl 2:3-11. Anadolu Kardiyol Derg. 2009. PMID: 20089481
-
Advances in congenital long QT syndrome.Curr Opin Pediatr. 2006 Oct;18(5):497-502. doi: 10.1097/01.mop.0000245349.30089.bf. Curr Opin Pediatr. 2006. PMID: 16969163 Review.
-
The Long QT Syndrome.Heart Lung Circ. 2007;16 Suppl 3:S5-12. doi: 10.1016/j.hlc.2007.05.008. Epub 2007 Jul 12. Heart Lung Circ. 2007. PMID: 17627884 Review.
-
Risk stratification in the long-QT syndrome.N Engl J Med. 2003 Aug 28;349(9):908-9; author reply 908-9. doi: 10.1056/NEJM200308283490916. N Engl J Med. 2003. PMID: 12944579 No abstract available.
-
Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome.Heart Rhythm. 2014 Jan;11(1):76-82. doi: 10.1016/j.hrthm.2013.10.005. Epub 2013 Oct 3. Heart Rhythm. 2014. PMID: 24096169
Cited by
-
Opportunities and challenges for identifying undiagnosed Rare Disease patients through analysis of primary care records: long QT syndrome as a test case.J Community Genet. 2024 Oct 15. doi: 10.1007/s12687-024-00742-7. Online ahead of print. J Community Genet. 2024. PMID: 39405009
-
Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death.Front Cardiovasc Med. 2023 Aug 4;10:1253479. doi: 10.3389/fcvm.2023.1253479. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37600027 Free PMC article. Review.
-
Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.Orphanet J Rare Dis. 2022 Oct 27;17(1):394. doi: 10.1186/s13023-022-02542-z. Orphanet J Rare Dis. 2022. PMID: 36303204 Free PMC article.
-
Paediatric/young versus adult patients with long QT syndrome.Open Heart. 2021 Sep;8(2):e001671. doi: 10.1136/openhrt-2021-001671. Open Heart. 2021. PMID: 34518285 Free PMC article.
-
Territory-Wide Chinese Cohort of Long QT Syndrome: Random Survival Forest and Cox Analyses.Front Cardiovasc Med. 2021 Feb 5;8:608592. doi: 10.3389/fcvm.2021.608592. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 33614747 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
