167 related articles for article (PubMed ID: 36448986)
1. Biological Life-Stage and the Burden of Cardiac Events in Women With Congenital Long QT Syndrome.
Younis A; Zareba W; Goldenberg I; Kharsa A; McNitt S; Aktas MK; Bodurian C; Farooq S; Polonsky B; Sotoodehnia N; Kudenchuk PJ; Rea TD; Arking DE; Luigi Bragazzi N; Goldenberg I
Circ Arrhythm Electrophysiol; 2022 Dec; 15(12):e011247. PubMed ID: 36448986
[No Abstract] [Full Text] [Related]
2. Risk Prediction in Women With Congenital Long QT Syndrome.
Goldenberg I; Bos JM; Yoruk A; Chen AY; Lopes C; Huang DT; Kutyifa V; Younis A; Aktas MK; Z Rosero S; McNitt S; Sotoodehnia N; Kudenchuk PJ; Rea TD; Arking DE; Scott CG; Briske KA; Sorensen K; J Ackerman M; Zareba W
J Am Heart Assoc; 2021 Jul; 10(14):e021088. PubMed ID: 34238014
[TBL] [Abstract][Full Text] [Related]
3. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
Vincent GM
Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
[TBL] [Abstract][Full Text] [Related]
4. Novel insights in the congenital long QT syndrome.
Wehrens XH; Vos MA; Doevendans PA; Wellens HJ
Ann Intern Med; 2002 Dec; 137(12):981-92. PubMed ID: 12484714
[TBL] [Abstract][Full Text] [Related]
5. [Ion channel disorders and arrhythmia--special reference to long QT syndrome and Brugada syndrome].
Shimizu W
Nihon Naika Gakkai Zasshi; 2006 Nov; 95(11):2321-9. PubMed ID: 17168410
[No Abstract] [Full Text] [Related]
6. 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]
7. [The long QT syndrome].
Garweg C; D'Orio V; Mélon P; Lancellotti P; Piérard LA
Rev Med Liege; 2010 Nov; 65(11):628-33. PubMed ID: 21189529
[TBL] [Abstract][Full Text] [Related]
8. The congenital long QT syndrome and implications for young athletes.
Kapetanopoulos A; Kluger J; Maron BJ; Thompson PD
Med Sci Sports Exerc; 2006 May; 38(5):816-25. PubMed ID: 16672832
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death].
Fosdal I; Wettrell G; Christiansen M; Kanters JK; Larsen LA
Lakartidningen; 2001 Feb; 98(8):810-5. PubMed ID: 11265565
[TBL] [Abstract][Full Text] [Related]
11. Summaries for patients. When the heart's electrical system goes haywire: the congenital long QT syndrome.
Ann Intern Med; 2002 Dec; 137(12):I43. PubMed ID: 12484739
[No Abstract] [Full Text] [Related]
12. Congenital long QT syndrome.
Crotti L; Celano G; Dagradi F; Schwartz PJ
Orphanet J Rare Dis; 2008 Jul; 3():18. PubMed ID: 18606002
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genotype- and phenotype-guided management of congenital long QT syndrome.
Giudicessi JR; Ackerman MJ
Curr Probl Cardiol; 2013 Oct; 38(10):417-55. PubMed ID: 24093767
[TBL] [Abstract][Full Text] [Related]
15. [Congenital long QT syndrome in newborns].
Emeriaud G; Douchin S; Jouk PS; Andrini P; Wroblewski I; Marey C; Rossignol AM
Arch Pediatr; 2002 Aug; 9(8):805-9. PubMed ID: 12205790
[TBL] [Abstract][Full Text] [Related]
16. Long QT syndrome: a preventable cause of sudden death in women.
Engelstein ED
Curr Womens Health Rep; 2003 Apr; 3(2):126-34. PubMed ID: 12628082
[TBL] [Abstract][Full Text] [Related]
17. The importance of the epinephrine provocation test for the hidden type-1 congenital long QT syndrome.
Atici A; Asoğlu R; Barman HA; Sahin I
Turk Kardiyol Dern Ars; 2020 Jun; 48(4):434-438. PubMed ID: 32519984
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age].
Akkerhuis JM; Baars HF; Marcelis CL; Akkerhuis KM; Wilde AA
Ned Tijdschr Geneeskd; 2007 Oct; 151(43):2357-64. PubMed ID: 18019210
[TBL] [Abstract][Full Text] [Related]
20. Genetic and clinical advances in congenital long QT syndrome.
Mizusawa Y; Horie M; Wilde AA
Circ J; 2014; 78(12):2827-33. PubMed ID: 25274057
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
