286 related articles for article (PubMed ID: 21831960)
61. Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
Allan WC; Timothy K; Vincent GM; Palomaki GE; Neveux LM; Haddow JE
J Med Screen; 2001; 8(4):173-7. PubMed ID: 11743032
[TBL] [Abstract][Full Text] [Related]
62. Clinical, genetic, and electrophysiologic characteristics of a new PAS-domain HERG mutation (M124R) causing Long QT syndrome.
Shushi L; Kerem B; Goldmit M; Peretz A; Attali B; Medina A; Towbin JA; Kurokawa J; Kass RS; Benhorin J
Ann Noninvasive Electrocardiol; 2005 Jul; 10(3):334-41. PubMed ID: 16029385
[TBL] [Abstract][Full Text] [Related]
63. Prognostic implications of mutation-specific QTc standard deviation in congenital long QT syndrome.
Mathias A; Moss AJ; Lopes CM; Barsheshet A; McNitt S; Zareba W; Robinson JL; Locati EH; Ackerman MJ; Benhorin J; Kaufman ES; Platonov PG; Qi M; Shimizu W; Towbin JA; Michael Vincent G; Wilde AA; Zhang L; Goldenberg I
Heart Rhythm; 2013 May; 10(5):720-5. PubMed ID: 23369741
[TBL] [Abstract][Full Text] [Related]
64. [A novel KCNQ1 mutation in Chinese with congenital long QT syndrome].
Liang L; Du ZD; Cai LL; Wu JX; Zheng T; Qi TX
Zhonghua Er Ke Za Zhi; 2003 Oct; 41(10):724-7. PubMed ID: 14731347
[TBL] [Abstract][Full Text] [Related]
65. The long QT syndromes: genetic basis and clinical implications.
Chiang CE; Roden DM
J Am Coll Cardiol; 2000 Jul; 36(1):1-12. PubMed ID: 10898405
[TBL] [Abstract][Full Text] [Related]
66. Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
Tester DJ; Medeiros-Domingo A; Will ML; Haglund CM; Ackerman MJ
Mayo Clin Proc; 2012 Jun; 87(6):524-39. PubMed ID: 22677073
[TBL] [Abstract][Full Text] [Related]
67. 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]
68. Risk stratification in the long-QT syndrome.
Priori SG; Schwartz PJ; Napolitano C; Bloise R; Ronchetti E; Grillo M; Vicentini A; Spazzolini C; Nastoli J; Bottelli G; Folli R; Cappelletti D
N Engl J Med; 2003 May; 348(19):1866-74. PubMed ID: 12736279
[TBL] [Abstract][Full Text] [Related]
69. Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome.
Earle N; Yeo Han D; Pilbrow A; Crawford J; Smith W; Shelling AN; Cameron V; Love DR; Skinner JR
Heart Rhythm; 2014 Jan; 11(1):76-82. PubMed ID: 24096169
[TBL] [Abstract][Full Text] [Related]
70. 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]
71. Efficacy of different beta-blockers in the treatment of long QT syndrome.
Abu-Zeitone A; Peterson DR; Polonsky B; McNitt S; Moss AJ
J Am Coll Cardiol; 2014 Sep; 64(13):1352-8. PubMed ID: 25257637
[TBL] [Abstract][Full Text] [Related]
72. Clinical implications for patients with long QT syndrome who experience a cardiac event during infancy.
Spazzolini C; Mullally J; Moss AJ; Schwartz PJ; McNitt S; Ouellet G; Fugate T; Goldenberg I; Jons C; Zareba W; Robinson JL; Ackerman MJ; Benhorin J; Crotti L; Kaufman ES; Locati EH; Qi M; Napolitano C; Priori SG; Towbin JA; Vincent GM
J Am Coll Cardiol; 2009 Aug; 54(9):832-7. PubMed ID: 19695463
[TBL] [Abstract][Full Text] [Related]
73. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
Moss AJ; Zareba W; Kaufman ES; Gartman E; Peterson DR; Benhorin J; Towbin JA; Keating MT; Priori SG; Schwartz PJ; Vincent GM; Robinson JL; Andrews ML; Feng C; Hall WJ; Medina A; Zhang L; Wang Z
Circulation; 2002 Feb; 105(7):794-9. PubMed ID: 11854117
[TBL] [Abstract][Full Text] [Related]
74. [DNA-based diagnostics of long QT syndrome].
Berge KE; Haugaa KH; Anfinsen OG; Früh A; Hallerud M; Jonsrud C; Øyen N; Gjesdal K; Amlie JP; Leren TP
Tidsskr Nor Laegeforen; 2005 Oct; 125(20):2783-6. PubMed ID: 16244680
[TBL] [Abstract][Full Text] [Related]
75. Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.
Paulussen A; Matthijs G; Gewillig M; Verhasselt P; Cohen N; Aerssens J
Genet Test; 2003; 7(1):57-61. PubMed ID: 12820704
[TBL] [Abstract][Full Text] [Related]
76. Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.
Khositseth A; Tester DJ; Will ML; Bell CM; Ackerman MJ
Heart Rhythm; 2004 May; 1(1):60-4. PubMed ID: 15851119
[TBL] [Abstract][Full Text] [Related]
77. Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.
Duchatelet S; Crotti L; Peat RA; Denjoy I; Itoh H; Berthet M; Ohno S; Fressart V; Monti MC; Crocamo C; Pedrazzini M; Dagradi F; Vicentini A; Klug D; Brink PA; Goosen A; Swan H; Toivonen L; Lahtinen AM; Kontula K; Shimizu W; Horie M; George AL; Trégouët DA; Guicheney P; Schwartz PJ
Circ Cardiovasc Genet; 2013 Aug; 6(4):354-61. PubMed ID: 23856471
[TBL] [Abstract][Full Text] [Related]
78. Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family.
Ichikawa M; Ohno S; Fujii Y; Ozawa J; Sonoda K; Fukuyama M; Kato K; Kimura H; Itoh H; Hayashi H; Horie M
Intern Med; 2016; 55(3):259-62. PubMed ID: 26831020
[TBL] [Abstract][Full Text] [Related]
79. Compound mutations: a common cause of severe long-QT syndrome.
Westenskow P; Splawski I; Timothy KW; Keating MT; Sanguinetti MC
Circulation; 2004 Apr; 109(15):1834-41. PubMed ID: 15051636
[TBL] [Abstract][Full Text] [Related]
80. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
