187 related articles for article (PubMed ID: 24133349)
1. Long QT syndrome: a Korean single center study.
Lee YS; Kwon BS; Kim GB; Oh SI; Bae EJ; Park SS; Noh CI
J Korean Med Sci; 2013 Oct; 28(10):1454-60. PubMed ID: 24133349
[TBL] [Abstract][Full Text] [Related]
2. Investigation of ion channel gene variants in patients with long QT syndrome.
Ernesto C; Cruz FE; Lima FS; Coutinho JL; Silva R; Urményi TP; Carvalho AC; Rondinelli E
Arq Bras Cardiol; 2011 Mar; 96(3):172-8. PubMed ID: 21308345
[TBL] [Abstract][Full Text] [Related]
3. Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A.
Seo SH; Kim SY; Cho SI; Park H; Lee S; Choi JM; Kim MJ; Lee JS; Ahn KJ; Song MK; Bae EJ; Park SS; Seong MW
Ann Lab Med; 2018 Jan; 38(1):54-58. PubMed ID: 29071820
[TBL] [Abstract][Full Text] [Related]
4. Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications.
Shinwari ZM; Al-Hazzani A; Dzimiri N; Tulbah S; Mallawi Y; Al-Fayyadh M; Al-Hassnan ZN
Clin Genet; 2013 Apr; 83(4):370-4. PubMed ID: 22708720
[TBL] [Abstract][Full Text] [Related]
5. Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.
Lieve KV; Williams L; Daly A; Richard G; Bale S; Macaya D; Chung WK
Genet Test Mol Biomarkers; 2013 Jul; 17(7):553-61. PubMed ID: 23631430
[TBL] [Abstract][Full Text] [Related]
6. Mutational spectrum of congenital long QT syndrome in Turkey; identification of 12 novel mutations across KCNQ1, KCNH2, SCN5A, KCNJ2, CACNA1C, and CALM1.
Akgun-Dogan O; Ağaoğlu NB; K Demirkol Y; Doğanay L; Ergül Y; Karacan M
J Cardiovasc Electrophysiol; 2022 Feb; 33(2):262-273. PubMed ID: 34860437
[TBL] [Abstract][Full Text] [Related]
7. Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome.
Theilade J; Kanters J; Henriksen FL; Gilså-Hansen M; Svendsen JH; Eschen O; Toft E; Reimers JI; Tybjærg-Hansen A; Christiansen M; Jensen HK; Bundgaard H
Cardiology; 2013; 126(2):131-7. PubMed ID: 23969902
[TBL] [Abstract][Full Text] [Related]
8. Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation.
Barsheshet A; Moss AJ; McNitt S; Polonsky S; Lopes CM; Zareba W; Robinson JL; Ackerman MJ; Benhorin J; Kaufman ES; Towbin JA; Vincent GM; Qi M; Goldenberg I
Circ Cardiovasc Genet; 2011 Oct; 4(5):491-9. PubMed ID: 21831960
[TBL] [Abstract][Full Text] [Related]
9. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322
[TBL] [Abstract][Full Text] [Related]
10. Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
Barc J; Briec F; Schmitt S; Kyndt F; Le Cunff M; Baron E; Vieyres C; Sacher F; Redon R; Le Caignec C; Le Marec H; Probst V; Schott JJ
J Am Coll Cardiol; 2011 Jan; 57(1):40-7. PubMed ID: 21185499
[TBL] [Abstract][Full Text] [Related]
11. [Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].
Shi RM; Ma AQ; Zhang YM; Yang C; Huang C; Zhou XH; Liu XH
Zhonghua Er Ke Za Zhi; 2009 Dec; 47(12):926-30. PubMed ID: 20193146
[TBL] [Abstract][Full Text] [Related]
12. Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.
Jimmy JJ; Chen CY; Yeh HM; Chiu WY; Yu CC; Liu YB; Tsai CT; Lo LW; Yeh SF; Lai LP
Chin Med J (Engl); 2014; 127(8):1482-6. PubMed ID: 24762593
[TBL] [Abstract][Full Text] [Related]
13. Long QT syndrome with mutations in three genes: A rare case.
Fernandes M; Martins Ribeiro S; Sanfins V; Lourenço A
Rev Port Cardiol; 2015 May; 34(5):359.e1-5. PubMed ID: 25935074
[TBL] [Abstract][Full Text] [Related]
14. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
Chang YS; Yang YW; Lin YN; Lin KH; Chang KC; Chang JG
Int Heart J; 2015; 56(4):450-3. PubMed ID: 26118593
[TBL] [Abstract][Full Text] [Related]
15. Mental stress test: a rapid, simple, and efficient test to unmask long QT syndrome.
Etienne P; Huchet F; Gaborit N; Barc J; Thollet A; Kyndt F; Guyomarch B; Le Marec H; Charpentier F; Schott JJ; Redon R; Probst V; Gourraud JB
Europace; 2018 Dec; 20(12):2014-2020. PubMed ID: 29688407
[TBL] [Abstract][Full Text] [Related]
16. An NGS-based genotyping in LQTS; minor genes are no longer minor.
Ohno S; Ozawa J; Fukuyama M; Makiyama T; Horie M
J Hum Genet; 2020 Dec; 65(12):1083-1091. PubMed ID: 32681117
[TBL] [Abstract][Full Text] [Related]
17. KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
Chen S; Zhang L; Bryant RM; Vincent GM; Flippin M; Lee JC; Brown E; Zimmerman F; Rozich R; Szafranski P; Oberti C; Sterba R; Marangi D; Tchou PJ; Chung MK; Wang Q
Clin Genet; 2003 Apr; 63(4):273-82. PubMed ID: 12702160
[TBL] [Abstract][Full Text] [Related]
18. Long QT and Brugada syndrome gene mutations in New Zealand.
Chung SK; MacCormick JM; McCulley CH; Crawford J; Eddy CA; Mitchell EA; Shelling AN; French JK; Skinner JR; Rees MI
Heart Rhythm; 2007 Oct; 4(10):1306-14. PubMed ID: 17905336
[TBL] [Abstract][Full Text] [Related]
19. Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.
Cuneo BF; Etheridge SP; Horigome H; Sallee D; Moon-Grady A; Weng HY; Ackerman MJ; Benson DW
Circ Arrhythm Electrophysiol; 2013 Oct; 6(5):946-51. PubMed ID: 23995044
[TBL] [Abstract][Full Text] [Related]
20. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
Winkel BG; Larsen MK; Berge KE; Leren TP; Nissen PH; Olesen MS; Hollegaard MV; Jespersen T; Yuan L; Nielsen N; Haunsø S; Svendsen JH; Wang Y; Kristensen IB; Jensen HK; Tfelt-Hansen J; Banner J
J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
