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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 2 |
2004 | 1 |
2016 | 1 |
2018 | 1 |
2024 | 0 |
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Compound mutations: a common cause of severe long-QT syndrome.
Circulation. 2004 Apr 20;109(15):1834-41. doi: 10.1161/01.CIR.0000125524.34234.13. Epub 2004 Mar 29.
Circulation. 2004.
PMID: 15051636
Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.
Wang DW, Yazawa K, George AL Jr, Bennett PB.
Wang DW, et al.
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13200-5. doi: 10.1073/pnas.93.23.13200.
Proc Natl Acad Sci U S A. 1996.
PMID: 8917568
Free PMC article.
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Multiple mechanisms of Na+ channel--linked long-QT syndrome.
Dumaine R, Wang Q, Keating MT, Hartmann HA, Schwartz PJ, Brown AM, Kirsch GE.
Dumaine R, et al.
Circ Res. 1996 May;78(5):916-24. doi: 10.1161/01.res.78.5.916.
Circ Res. 1996.
PMID: 8620612
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Genetic and Phenotypic Characterization of Community Hospital Patients With QT Prolongation.
Gibbs C, Thalamus J, Tveten K, Busk ØL, Hysing J, Haugaa KH, Holla ØL.
Gibbs C, et al.
J Am Heart Assoc. 2018 Aug 21;7(16):e009706. doi: 10.1161/JAHA.118.009706.
J Am Heart Assoc. 2018.
PMID: 30369311
Free PMC article.
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Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction.
Malan D, Zhang M, Stallmeyer B, Müller J, Fleischmann BK, Schulze-Bahr E, Sasse P, Greber B.
Malan D, et al.
Basic Res Cardiol. 2016 Mar;111(2):14. doi: 10.1007/s00395-016-0530-0. Epub 2016 Jan 23.
Basic Res Cardiol. 2016.
PMID: 26803770
Free PMC article.
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