286 related articles for article (PubMed ID: 21831960)
81. Determination and Interpretation of the QT Interval.
Vink AS; Neumann B; Lieve KVV; Sinner MF; Hofman N; El Kadi S; Schoenmaker MHA; Slaghekke HMJ; de Jong JSSG; Clur SB; Blom NA; Kääb S; Wilde AAM; Postema PG
Circulation; 2018 Nov; 138(21):2345-2358. PubMed ID: 30571576
[TBL] [Abstract][Full Text] [Related]
82. Mutation-specific risk in two genetic forms of type 3 long QT syndrome.
Liu JF; Moss AJ; Jons C; Benhorin J; Schwartz PJ; Spazzolini C; Crotti L; Ackerman MJ; McNitt S; Robinson JL; Qi M; Goldenberg I; Zareba W
Am J Cardiol; 2010 Jan; 105(2):210-3. PubMed ID: 20102920
[TBL] [Abstract][Full Text] [Related]
83. Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.
Horigome H; Nagashima M; Sumitomo N; Yoshinaga M; Ushinohama H; Iwamoto M; Shiono J; Ichihashi K; Hasegawa S; Yoshikawa T; Matsunaga T; Goto H; Waki K; Arima M; Takasugi H; Tanaka Y; Tauchi N; Ikoma M; Inamura N; Takahashi H; Shimizu W; Horie M
Circ Arrhythm Electrophysiol; 2010 Feb; 3(1):10-7. PubMed ID: 19996378
[TBL] [Abstract][Full Text] [Related]
84. Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ1 and KCNH2 gene mutations: importance of exercise testing.
Andrsova I; Novotny T; Kadlecova J; Bittnerova A; Vit P; Florianova A; Sisakova M; Gaillyova R; Manouskova L; Spinar J
J Electrocardiol; 2012; 45(6):746-51. PubMed ID: 22727609
[TBL] [Abstract][Full Text] [Related]
85. KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L; Lundquist AL; Insolia R; Pedrazzini M; Ferrandi C; De Ferrari GM; Vicentini A; Yang P; Roden DM; George AL; Schwartz PJ
Circulation; 2005 Aug; 112(9):1251-8. PubMed ID: 16116052
[TBL] [Abstract][Full Text] [Related]
86. Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.
Allegue C; Gil R; Blanco-Verea A; Santori M; Rodríguez-Calvo M; Concheiro L; Carracedo A; Brion M
Int J Legal Med; 2011 Jul; 125(4):565-72. PubMed ID: 21499742
[TBL] [Abstract][Full Text] [Related]
87. Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.
Grunnet M; Behr ER; Calloe K; Hofman-Bang J; Till J; Christiansen M; McKenna WJ; Olesen SP; Schmitt N
Heart Rhythm; 2005 Nov; 2(11):1238-49. PubMed ID: 16253915
[TBL] [Abstract][Full Text] [Related]
88. A challenge for mutation specific risk stratification in long QT syndrome type 1.
Yagi N; Itoh H; Hisamatsu T; Tomita Y; Kimura H; Fujii Y; Makiyama T; Horie M; Ohno S
J Cardiol; 2018 Jul; 72(1):56-65. PubMed ID: 29439887
[TBL] [Abstract][Full Text] [Related]
89. Aborted Cardiac Arrest in LQT2 Related to Novel
Bileišienė N; Barysienė J; Mikštienė V; Preikšaitienė E; Marinskis G; Keževičiūtė M; Utkus A; Aidietis A
Medicina (Kaunas); 2021 Jul; 57(7):. PubMed ID: 34357002
[TBL] [Abstract][Full Text] [Related]
90. Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.
Shimizu W; Horie M; Ohno S; Takenaka K; Yamaguchi M; Shimizu M; Washizuka T; Aizawa Y; Nakamura K; Ohe T; Aiba T; Miyamoto Y; Yoshimasa Y; Towbin JA; Priori SG; Kamakura S
J Am Coll Cardiol; 2004 Jul; 44(1):117-25. PubMed ID: 15234419
[TBL] [Abstract][Full Text] [Related]
91. Elucidation of
Zhou W; Ye D; Tester DJ; Bains S; Giudicessi JR; Haglund-Turnquist CM; Orland KM; January CT; Eckhardt LL; Maginot KR; Ackerman MJ
Circ Genom Precis Med; 2023 Apr; 16(2):e003726. PubMed ID: 37071726
[TBL] [Abstract][Full Text] [Related]
92. 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]
93. Long QT syndrome in patients over 40 years of age: increased risk for LQTS-related cardiac events in patients with coronary disease.
Sze E; Moss AJ; Goldenberg I; McNitt S; Jons C; Zareba W; Qi M; Robinson JL;
Ann Noninvasive Electrocardiol; 2008 Oct; 13(4):327-31. PubMed ID: 18973489
[TBL] [Abstract][Full Text] [Related]
94. Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.
Tester DJ; Medeiros-Domingo A; Will ML; Ackerman MJ
Mayo Clin Proc; 2011 Oct; 86(10):941-7. PubMed ID: 21964171
[TBL] [Abstract][Full Text] [Related]
95. Ion channel mechanisms related to sudden cardiac death in phenotype-negative long-QT syndrome genotype-phenotype correlations of the KCNQ1(S349W) mutation.
Horr S; Goldenberg I; Moss AJ; O-Uchi J; Barsheshet A; Connelly H; Gray DA; Zareba W; Lopes CM
J Cardiovasc Electrophysiol; 2011 Feb; 22(2):193-200. PubMed ID: 20662986
[TBL] [Abstract][Full Text] [Related]
96. Molecular autopsy for sudden unexplained death? Time to discuss pros and cons.
Mazzanti A; Priori SG
J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1099-102. PubMed ID: 22966897
[No Abstract] [Full Text] [Related]
97. 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]
98. Elevated heart rate triggers action potential alternans and sudden death. translational study of a homozygous KCNH2 mutation.
Schweigmann U; Biliczki P; Ramirez RJ; Marschall C; Takac I; Brandes RP; Kotzot D; Girmatsion Z; Hohnloser SH; Ehrlich JR
PLoS One; 2014; 9(8):e103150. PubMed ID: 25140878
[TBL] [Abstract][Full Text] [Related]
99. Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.
Choi G; Kopplin LJ; Tester DJ; Will ML; Haglund CM; Ackerman MJ
Circulation; 2004 Oct; 110(15):2119-24. PubMed ID: 15466642
[TBL] [Abstract][Full Text] [Related]
100. The inherited long QT syndrome: from ion channel to bedside.
Vincent GM; Timothy K; Fox J; Zhang L
Cardiol Rev; 1999; 7(1):44-55. PubMed ID: 10348966
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
