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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 1 |
1999 | 2 |
2001 | 1 |
2012 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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6 results
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Page 1
Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome.
Mayo Clin Proc. 1999 Nov;74(11):1088-94. doi: 10.4065/74.11.1088.
Mayo Clin Proc. 1999.
PMID: 10560595
Jervell and Lange-Nielsen syndrome: a Norwegian perspective.
Tranebjaerg L, Bathen J, Tyson J, Bitner-Glindzicz M.
Tranebjaerg L, et al.
Am J Med Genet. 1999 Sep 24;89(3):137-46.
Am J Med Genet. 1999.
PMID: 10704188
Review.
Item in Clipboard
A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen syndrome.
Huang L, Bitner-Glindzicz M, Tranebjaerg L, Tinker A.
Huang L, et al.
Cardiovasc Res. 2001 Sep;51(4):670-80. doi: 10.1016/s0008-6363(01)00350-9.
Cardiovasc Res. 2001.
PMID: 11530100
Item in Clipboard
Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden.
Winbo A, Stattin EL, Diamant UB, Persson J, Jensen SM, Rydberg A.
Winbo A, et al.
Europace. 2012 Dec;14(12):1799-806. doi: 10.1093/europace/eus111. Epub 2012 Apr 26.
Europace. 2012.
PMID: 22539601
Item in Clipboard
Marked, transient, emotion-triggered QT accentuation in an adolescent female with type 1 long QT syndrome.
Anderson HN, Medford BA, Ackerman MJ.
Anderson HN, et al.
Cardiol Young. 2015 Feb;25(2):376-9. doi: 10.1017/S1047951114000213. Epub 2014 Mar 26.
Cardiol Young. 2015.
PMID: 24666684
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IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M.
Tyson J, et al.
Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179.
Hum Mol Genet. 1997.
PMID: 9328483
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