138 related articles for article (PubMed ID: 20960620)
1. Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L; Pedrazzini M; Ferrandi C; Insolia R; Cuoretti A; Dagradi F; Crimi G; Coto E; Reguero JR; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):543. PubMed ID: 20960620
[No Abstract] [Full Text] [Related]
2. Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L; Pedrazzini M; Insolia R; Ferrandi C; Cuoretti A; Celano G; Gandolfi E; Dagradi F; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):541. PubMed ID: 20960616
[No Abstract] [Full Text] [Related]
3. Gene symbol: KCNH2. Disease: Long QT syndrome.
Crotti L; Crotti L; Pedrazzini M; Insolia R; Ferrandi C; Cuoretti A; Gandolfi E; Celano G; Dagradi F; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):540. PubMed ID: 20960613
[No Abstract] [Full Text] [Related]
4. [A novel mutation of the KCNH2 gene in a family with congenital long QT syndrome].
Lian J; Zhou J; Huang X; Wang Y; Yang X; Li D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb; 27(1):77-80. PubMed ID: 20140874
[TBL] [Abstract][Full Text] [Related]
5. Congenital long QT syndrome with compound mutations in the KCNH2 gene.
Bando S; Soeki T; Matsuura T; Niki T; Ise T; Yamaguchi K; Taketani Y; Iwase T; Yamada H; Wakatsuki T; Akaike M; Aiba T; Shimizu W; Sata M
Heart Vessels; 2014 Jul; 29(4):554-9. PubMed ID: 24057343
[TBL] [Abstract][Full Text] [Related]
6. Gene symbol: KCNH2.
Crotti L; Pedrazzini M; Ferrandi C; Insolia R; Tosin L; Vicentini A; Turco A; De Ferrari GM; Schwartz PJ
Hum Genet; 2007 Feb; 120(6):912. PubMed ID: 17438608
[No Abstract] [Full Text] [Related]
7. Novel mutation in the KCNH2 gene associated with long QT syndrome.
Silva D; Miltenberger-Miltenyi G; Correia MJ; Diogo AN
Rev Port Cardiol; 2013 Feb; 32(2):163-4. PubMed ID: 23351921
[No Abstract] [Full Text] [Related]
8. QT interval prolongation in a patient with LQT2 on levetiracetam.
Issa NP; Fisher WG; Narayanan JT
Seizure; 2015 Jul; 29():134-6. PubMed ID: 26076856
[No Abstract] [Full Text] [Related]
9. Gene symbol: KCNH2.
Crotti L; Insolia R; Pedrazzini M; Andreoli C; Gabanti E; Moncalvo C; Crimi G; De Ferrari GM; Schwartz PJ
Hum Genet; 2007 Feb; 120(6):911. PubMed ID: 17438606
[No Abstract] [Full Text] [Related]
10. Gene symbol: KCNQ1. Disease: Long QT syndrome.
Crotti L; Ferrandi C; Pedrazzini M; Insolia R; Cuoretti A; Celano G; Dagradi F; Stramba-Badiale M; Schwartz PJ
Hum Genet; 2008 Jun; 123(5):543. PubMed ID: 20960619
[No Abstract] [Full Text] [Related]
11. Not all pathogenic mutations are pathogenic: KCNH2 mutations in two sisters with tetralogy of Fallot.
Bhuiyan ZA; Alswaid A; Belfiore M; Al-Ghamdi SS; Liang J; Schlaepffer J
Int J Cardiol; 2014 Mar; 172(1):276-7. PubMed ID: 24462143
[No Abstract] [Full Text] [Related]
12. Long QT syndrome.
Abrams DJ; Macrae CA
Circulation; 2014 Apr; 129(14):1524-9. PubMed ID: 24709866
[No Abstract] [Full Text] [Related]
13. Quantification of repolarization morphology in the long QT-syndrome in the genomic era.
van den Berg MP; van Tintelen JP
Heart Rhythm; 2006 Dec; 3(12):1467-8. PubMed ID: 17161790
[No Abstract] [Full Text] [Related]
14. [The long QT syndrome from the bedside to molecular genetic laboratory. The history of the first described Hungarian family].
Csanády M; Sepp R
Orv Hetil; 2005 Sep; 146(39):2011-6. PubMed ID: 16265869
[TBL] [Abstract][Full Text] [Related]
15. Neonatal heart block and long-QT syndrome.
Sy RW; Hamilton R; Klein GJ; Krahn AD
J Cardiovasc Electrophysiol; 2010 Sep; 21(9):1059-60. PubMed ID: 20455980
[No Abstract] [Full Text] [Related]
16. [KCNH2 gene new mutation in a patient with prior diagnosis of epilepsy].
Chanséaume A; Millat G; Roux A
Rev Neurol (Paris); 2014 Apr; 170(4):304-5. PubMed ID: 24679481
[No Abstract] [Full Text] [Related]
17. ECGs in the ED.
Tanel RE
Pediatr Emerg Care; 2014 Aug; 30(8):588-9. PubMed ID: 25098809
[No Abstract] [Full Text] [Related]
18. A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1.
Yoshikane Y; Yoshinaga M; Hamamoto K; Hirose S
Heart Rhythm; 2013 Apr; 10(4):600-3. PubMed ID: 23237912
[No Abstract] [Full Text] [Related]
19. A family of hereditary long QT syndrome caused by Q738X HERG mutation.
Yasuda S; Hiramatsu S; Odashiro K; Maruyama T; Tsuji K; Horie M
Int J Cardiol; 2010 Sep; 144(1):69-72. PubMed ID: 19157587
[No Abstract] [Full Text] [Related]
20. [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]
[Next] [New Search]