281 related articles for article (PubMed ID: 9511785)
1. The long QT syndrome: ion channel diseases of the heart.
Ackerman MJ
Mayo Clin Proc; 1998 Mar; 73(3):250-69. PubMed ID: 9511785
[TBL] [Abstract][Full Text] [Related]
2. [Molecular genetics in the hereditary form of long QT syndrome].
Georgijević Milić L
Med Pregl; 2000; 53(1-2):51-4. PubMed ID: 10953551
[TBL] [Abstract][Full Text] [Related]
3. [Electrocardiogram in channel disorders].
González-Hermosillo JA
Arch Cardiol Mex; 2004; 74 Suppl 1():S79-83. PubMed ID: 15216752
[TBL] [Abstract][Full Text] [Related]
4. [Molecular genetics of the long QT syndrome: clinical aspects].
Sepp R; Csanády M
Orv Hetil; 1999 Nov; 140(47):2633-8. PubMed ID: 10613047
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome.
Duggal P; Vesely MR; Wattanasirichaigoon D; Villafane J; Kaushik V; Beggs AH
Circulation; 1998 Jan; 97(2):142-6. PubMed ID: 9445165
[TBL] [Abstract][Full Text] [Related]
7. Molecular biology of the long QT syndrome: impact on management.
Priori SG; Napolitano C; Paganini V; Cantù F; Schwartz PJ
Pacing Clin Electrophysiol; 1997 Aug; 20(8 Pt 2):2052-7. PubMed ID: 9272507
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [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]
11. Characterization of a KCNQ1/KVLQT1 polymorphism in Asian families with LQT2: implications for genetic testing.
Sharma D; Glatter KA; Timofeyev V; Tuteja D; Zhang Z; Rodriguez J; Tester DJ; Low R; Scheinman MM; Ackerman MJ; Chiamvimonvat N
J Mol Cell Cardiol; 2004 Jul; 37(1):79-89. PubMed ID: 15242738
[TBL] [Abstract][Full Text] [Related]
12. Cellular basis for long QT, transmural dispersion of repolarization, and torsade de pointes in the long QT syndrome.
Shimizu W; Antzelevitch C
J Electrocardiol; 1999; 32 Suppl():177-84. PubMed ID: 10688323
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biology.
Priori SG; Cantù F; Schwartz PJ
Schweiz Med Wochenschr; 1996 Oct; 126(41):1727-31. PubMed ID: 8893413
[TBL] [Abstract][Full Text] [Related]
17. Molecular biology and the prolonged QT syndromes.
Towbin JA; Vatta M
Am J Med; 2001 Apr; 110(5):385-98. PubMed ID: 11286954
[TBL] [Abstract][Full Text] [Related]
18. [Value of genetic testing in the management of the congenital long QT syndrome].
Lupoglazoff JM; Denjoy I; Guicheney P
Arch Mal Coeur Vaiss; 2003 May; 96(5):539-47. PubMed ID: 12838849
[TBL] [Abstract][Full Text] [Related]
19. Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
Splawski I; Shen J; Timothy KW; Lehmann MH; Priori S; Robinson JL; Moss AJ; Schwartz PJ; Towbin JA; Vincent GM; Keating MT
Circulation; 2000 Sep; 102(10):1178-85. PubMed ID: 10973849
[TBL] [Abstract][Full Text] [Related]
20. Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.
Diamant UB; Vahedi F; Winbo A; Rydberg A; Stattin EL; Jensen SM; Bergfeldt L
J Appl Physiol (1985); 2013 Nov; 115(10):1423-32. PubMed ID: 24052033
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]