223 related articles for article (PubMed ID: 34755423)
1. Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early-onset long QT syndrome and sinoatrial node dysfunction.
Yang Z; Ma Y; Huang J; Xian J; Huang Y; Wu L; Zhu W; Wang F; Chen L; Lin X; Lin Y
Ann Noninvasive Electrocardiol; 2022 Jan; 27(1):e12889. PubMed ID: 34755423
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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.
Chen J; Li H; Guo S; Yang Z; Sun S; Zeng J; Gou H; Chen Y; Wang F; Lin Y; Huang K; Yue H; Ma Y; Lin Y
Orphanet J Rare Dis; 2022 Oct; 17(1):394. PubMed ID: 36303204
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
6. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. 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]
10. Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
Christiansen M; Hedley PL; Theilade J; Stoevring B; Leren TP; Eschen O; Sørensen KM; Tybjærg-Hansen A; Ousager LB; Pedersen LN; Frikke-Schmidt R; Aidt FH; Hansen MG; Hansen J; Bloch Thomsen PE; Toft E; Henriksen FL; Bundgaard H; Jensen HK; Kanters JK
BMC Med Genet; 2014 Mar; 15():31. PubMed ID: 24606995
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
Wang F; Liu Y; Liao H; Xue Y; Zhan X; Fang X; Liang Y; Wei W; Rao F; Zhang Q; Deng H; Lin Y; Liu F; Lin W; Zhang B; Wu S
Cardiology; 2020; 145(1):38-45. PubMed ID: 31751991
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
Antzelevitch C
J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
[TBL] [Abstract][Full Text] [Related]
16. Genetics of long QT syndrome.
Tester DJ; Ackerman MJ
Methodist Debakey Cardiovasc J; 2014; 10(1):29-33. PubMed ID: 24932360
[TBL] [Abstract][Full Text] [Related]
17. Long QT syndrome-associated mutations in intrauterine fetal death.
Crotti L; Tester DJ; White WM; Bartos DC; Insolia R; Besana A; Kunic JD; Will ML; Velasco EJ; Bair JJ; Ghidoni A; Cetin I; Van Dyke DL; Wick MJ; Brost B; Delisle BP; Facchinetti F; George AL; Schwartz PJ; Ackerman MJ
JAMA; 2013 Apr; 309(14):1473-82. PubMed ID: 23571586
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the transmembrane nonpore region of the KCNH2 gene causes severe clinical manifestations of long QT syndrome.
Liu L; Hayashi K; Kaneda T; Ino H; Fujino N; Uchiyama K; Konno T; Tsuda T; Kawashiri MA; Ueda K; Higashikata T; Shuai W; Kupershmidt S; Higashida H; Yamagishi M
Heart Rhythm; 2013 Jan; 10(1):61-7. PubMed ID: 23010577
[TBL] [Abstract][Full Text] [Related]
19. Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
Kapa S; Tester DJ; Salisbury BA; Harris-Kerr C; Pungliya MS; Alders M; Wilde AA; Ackerman MJ
Circulation; 2009 Nov; 120(18):1752-60. PubMed ID: 19841300
[TBL] [Abstract][Full Text] [Related]
20. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
Tester DJ; Cronk LB; Carr JL; Schulz V; Salisbury BA; Judson RS; Ackerman MJ
Heart Rhythm; 2006 Jul; 3(7):815-21. PubMed ID: 16818214
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
