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Results: 1 to 20 of 113

1.

The long QT syndrome: ion channel diseases of the heart.

Ackerman MJ.

Mayo Clin Proc. 1998 Mar;73(3):250-69. Review.

PMID:
9511785
[PubMed - indexed for MEDLINE]
2.

[Molecular genetics in the hereditary form of long QT syndrome].

Georgijević Milić L.

Med Pregl. 2000 Jan-Feb;53(1-2):51-4. Review. Croatian.

PMID:
10953551
[PubMed - indexed for MEDLINE]
3.

[Electrocardiogram in channel disorders].

González-Hermosillo JA.

Arch Cardiol Mex. 2004 Jan-Mar;74 Suppl 1:S79-83. Review. Spanish.

PMID:
15216752
[PubMed - indexed for MEDLINE]
4.

[Molecular genetics of the long QT syndrome: clinical aspects].

Sepp R, Csanády M.

Orv Hetil. 1999 Nov 21;140(47):2633-8. Review. Hungarian.

PMID:
10613047
[PubMed - indexed for MEDLINE]
5.

The long QT syndromes: genetic basis and clinical implications.

Chiang CE, Roden DM.

J Am Coll Cardiol. 2000 Jul;36(1):1-12. Review.

PMID:
10898405
[PubMed - indexed for MEDLINE]
Free Article
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 20;97(2):142-6.

PMID:
9445165
[PubMed - indexed for MEDLINE]
Free Article
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. Review.

PMID:
9272507
[PubMed - indexed for MEDLINE]
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.

PMID:
10868746
[PubMed - indexed for MEDLINE]
9.

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.

Vincent GM.

Annu Rev Med. 1998;49:263-74. Review.

PMID:
9509262
[PubMed - indexed for MEDLINE]
10.

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.

PMID:
15242738
[PubMed - indexed for MEDLINE]
11.

[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. Review. French.

PMID:
10816797
[PubMed - indexed for MEDLINE]
12.

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. Review.

PMID:
9791861
[PubMed - indexed for MEDLINE]
13.

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. Review.

PMID:
10688323
[PubMed - indexed for MEDLINE]
14.

The inherited long QT syndrome: from ion channel to bedside.

Vincent GM, Timothy K, Fox J, Zhang L.

Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Review.

PMID:
10348966
[PubMed - indexed for MEDLINE]
15.

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

Chen Q, Zhang D, Gingell RL, Moss AJ, Napolitano C, Priori SG, Schwartz PJ, Kehoe E, Robinson JL, Schulze-Bahr E, Wang Q, Towbin JA.

Circulation. 1999 Mar 16;99(10):1344-7.

PMID:
10077519
[PubMed - indexed for MEDLINE]
Free Article
16.

Molecular biology and the prolonged QT syndromes.

Towbin JA, Vatta M.

Am J Med. 2001 Apr 1;110(5):385-98. Review.

PMID:
11286954
[PubMed - indexed for MEDLINE]
17.

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 12;126(41):1727-31.

PMID:
8893413
[PubMed - indexed for MEDLINE]
18.

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene.

van den Berg MH, Wilde AA, Robles de Medina EO, Meyer H, Geelen JL, Jongbloed RJ, Wellens HJ, Geraedts JP.

Hum Genet. 1997 Sep;100(3-4):356-61.

PMID:
9272155
[PubMed - indexed for MEDLINE]
19.

[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. Review. French.

PMID:
12838849
[PubMed - indexed for MEDLINE]
20.

Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.

Swan H, Viitasalo M, Piippo K, Laitinen P, Kontula K, Toivonen L.

J Am Coll Cardiol. 1999 Sep;34(3):823-9.

PMID:
10483966
[PubMed - indexed for MEDLINE]
Free Article

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