772 related articles for article (PubMed ID: 10953551)
21. [Present concepts of congenital long QT syndrome].
Leenhardt A; Denjoy I; Maison-Blanche P; Guicheney P; Coumel P
Arch Mal Coeur Vaiss; 2000 Apr; 93(3 Spec No):17-21. PubMed ID: 10816797
[TBL] [Abstract][Full Text] [Related]
22. Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome.
Frank-Hansen R; Larsen LA; Andersen P; Jespersgaard C; Christiansen M
Clin Chim Acta; 2005 Jan; 351(1-2):95-100. PubMed ID: 15563876
[TBL] [Abstract][Full Text] [Related]
23. Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction.
Chen J; Makiyama T; Wuriyanghai Y; Ohno S; Sasaki K; Hayano M; Harita T; Nishiuchi S; Yuta Yamamoto ; Ueyama T; Shimizu A; Horie M; Kimura T
Heart Rhythm; 2016 Jan; 13(1):289-98. PubMed ID: 26282245
[TBL] [Abstract][Full Text] [Related]
24. The molecular basis of long QT syndrome and prospects for therapy.
Wang Q; Bowles NE; Towbin JA
Mol Med Today; 1998 Sep; 4(9):382-8. PubMed ID: 9791861
[TBL] [Abstract][Full Text] [Related]
25. Molecular genetics of long-QT syndrome.
Wattanasirichaigoon D; Beggs AH
Curr Opin Pediatr; 1998 Dec; 10(6):628-34. PubMed ID: 9848024
[TBL] [Abstract][Full Text] [Related]
26. Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome.
Priori SG; Napolitano C; Cantù F; Brown AM; Schwartz PJ
Circ Res; 1996 Jun; 78(6):1009-15. PubMed ID: 8635231
[TBL] [Abstract][Full Text] [Related]
27. Sodium channel abnormalities are infrequent in patients with long QT syndrome: identification of two novel SCN5A mutations.
Wattanasirichaigoon D; Vesely MR; Duggal P; Levine JC; Blume ED; Wolff GS; Edwards SB; Beggs AH
Am J Med Genet; 1999 Oct; 86(5):470-6. PubMed ID: 10508990
[TBL] [Abstract][Full Text] [Related]
28. Gene-specific differences in the circadian variation of ventricular repolarization in the long QT syndrome: a key to sudden death during sleep?
Stramba-Badiale M; Priori SG; Napolitano C; Locati EH; Viñolas X; Haverkamp W; Schulze-Bahr E; Goulene K; Schwartz PJ
Ital Heart J; 2000 May; 1(5):323-8. PubMed ID: 10832806
[TBL] [Abstract][Full Text] [Related]
29. DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
Jongbloed R; Marcelis C; Velter C; Doevendans P; Geraedts J; Smeets H
Hum Mutat; 2002 Nov; 20(5):382-91. PubMed ID: 12402336
[TBL] [Abstract][Full Text] [Related]
30. The long QT syndrome: therapeutic implications of a genetic diagnosis.
Shimizu W
Cardiovasc Res; 2005 Aug; 67(3):347-56. PubMed ID: 15979599
[TBL] [Abstract][Full Text] [Related]
31. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.
Chouabe C; Neyroud N; Guicheney P; Lazdunski M; Romey G; Barhanin J
EMBO J; 1997 Sep; 16(17):5472-9. PubMed ID: 9312006
[TBL] [Abstract][Full Text] [Related]
32. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
Thomas D; Wimmer AB; Karle CA; Licka M; Alter M; Khalil M; Ulmer HE; Kathöfer S; Kiehn J; Katus HA; Schoels W; Koenen M; Zehelein J
Cardiovasc Res; 2005 Aug; 67(3):487-97. PubMed ID: 15950200
[TBL] [Abstract][Full Text] [Related]
33. Genetics of long-QT syndrome.
Nakano Y; Shimizu W
J Hum Genet; 2016 Jan; 61(1):51-5. PubMed ID: 26108145
[TBL] [Abstract][Full Text] [Related]
34. Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
Ohno S; Toyoda F; Zankov DP; Yoshida H; Makiyama T; Tsuji K; Honda T; Obayashi K; Ueyama H; Shimizu W; Miyamoto Y; Kamakura S; Matsuura H; Kita T; Horie M
Hum Mutat; 2009 Apr; 30(4):557-63. PubMed ID: 19306396
[TBL] [Abstract][Full Text] [Related]
35. Long QT syndrome: ionic basis and arrhythmia mechanism in long QT syndrome type 1.
Sanguinetti MC
J Cardiovasc Electrophysiol; 2000 Jun; 11(6):710-2. PubMed ID: 10868746
[TBL] [Abstract][Full Text] [Related]
36. In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant.
Lin MT; Wu MH; Chang CC; Chiu SN; Thériault O; Huang H; Christé G; Ficker E; Chahine M
Heart Rhythm; 2008 Nov; 5(11):1567-74. PubMed ID: 18848812
[TBL] [Abstract][Full Text] [Related]
37. Functional effects of a missense mutation in HERG associated with type 2 long QT syndrome.
Amorós I; Jiménez-Jáimez J; Tercedor L; Barana A; Gómez R; de la Fuente MG; Dolz-Gaitón P; Alvarez M; Martínez-Espín E; Lorente JA; Melgares R; Tamargo J; Delpón E; Caballero R
Heart Rhythm; 2011 Mar; 8(3):463-70. PubMed ID: 21109023
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. [Inborn long QT-syndrome in childhood: clinical presentation and treatment].
Ulmer HE; Khalil M; Fischer M; Brockmeier K
Herzschrittmacherther Elektrophysiol; 2002 Sep; 13(3):130-41. PubMed ID: 24535447
[TBL] [Abstract][Full Text] [Related]
40. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
Tester DJ; Will ML; Haglund CM; Ackerman MJ
Heart Rhythm; 2005 May; 2(5):507-17. PubMed ID: 15840476
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
