711 related articles for article (PubMed ID: 10613047)
1. [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]
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. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
Neyroud N; Tesson F; Denjoy I; Leibovici M; Donger C; Barhanin J; Fauré S; Gary F; Coumel P; Petit C; Schwartz K; Guicheney P
Nat Genet; 1997 Feb; 15(2):186-9. PubMed ID: 9020846
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. The genetic basis of long QT and short QT syndromes: a mutation update.
Hedley PL; Jørgensen P; Schlamowitz S; Wangari R; Moolman-Smook J; Brink PA; Kanters JK; Corfield VA; Christiansen M
Hum Mutat; 2009 Nov; 30(11):1486-511. PubMed ID: 19862833
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Molecular mechanisms of arrhythmias.
Janse MJ; Wilde AA
Rev Port Cardiol; 1998 Oct; 17 Suppl 2():II41-6. PubMed ID: 9835781
[TBL] [Abstract][Full Text] [Related]
8. Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.
Ching CK; Tan EC
Expert Rev Mol Diagn; 2006 May; 6(3):365-74. PubMed ID: 16706739
[TBL] [Abstract][Full Text] [Related]
9. [Long QT syndrome].
Nakajima T; Kaneko Y; Taniguchi Y; Nagai R
Nihon Rinsho; 1996 Mar; 54(3):776-81. PubMed ID: 8904236
[TBL] [Abstract][Full Text] [Related]
10. HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.
Paulussen AD; Raes A; Jongbloed RJ; Gilissen RA; Wilde AA; Snyders DJ; Smeets HJ; Aerssens J
Cardiovasc Res; 2005 Aug; 67(3):467-75. PubMed ID: 15958262
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Genetics, molecular mechanisms and management of long QT syndrome.
Wang Q; Chen Q; Towbin JA
Ann Med; 1998 Feb; 30(1):58-65. PubMed ID: 9556090
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Molecular physiology of cardiac delayed rectifier K+ channels.
Sanguinetti MC; Zou A
Heart Vessels; 1997; Suppl 12():170-2. PubMed ID: 9476573
[TBL] [Abstract][Full Text] [Related]
16. Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.
Berge KE; Haugaa KH; Früh A; Anfinsen OG; Gjesdal K; Siem G; Oyen N; Greve G; Carlsson A; Rognum TO; Hallerud M; Kongsgård E; Amlie JP; Leren TP
Scand J Clin Lab Invest; 2008; 68(5):362-8. PubMed ID: 18752142
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Two components of delayed rectifier K+ current in heart: molecular basis, functional diversity, and contribution to repolarization.
Cheng JH; Kodama I
Acta Pharmacol Sin; 2004 Feb; 25(2):137-45. PubMed ID: 14769199
[TBL] [Abstract][Full Text] [Related]
20. Cardiac K+ channels and drug-acquired long QT syndrome.
Drici MD; Barhanin J
Therapie; 2000; 55(1):185-93. PubMed ID: 10860023
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]