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Results: 8

1.

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT.

Nat Genet. 1996 Jan;12(1):17-23.

PMID:
8528244
[PubMed - indexed for MEDLINE]
2.

Genetics, molecular mechanisms and management of long QT syndrome.

Wang Q, Chen Q, Towbin JA.

Ann Med. 1998 Feb;30(1):58-65. Review.

PMID:
9556090
[PubMed - indexed for MEDLINE]
3.

Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.

Sanguinetti MC.

Ann N Y Acad Sci. 1999 Apr 30;868:406-13. Review.

PMID:
10414310
[PubMed - indexed for MEDLINE]
4.

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
[PubMed - indexed for MEDLINE]
5.

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]
6.

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]
7.

KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome.

Herbert E, Trusz-Gluza M, Moric E, Smiłowska-Dzielicka E, Mazurek U, Wilczok T.

Med Sci Monit. 2002 Oct;8(10):RA240-8. Review.

PMID:
12388934
[PubMed - indexed for MEDLINE]
8.

[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]

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