Schmitt N - Search Results

1

IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation.

Steffensen AB, Refsgaard L, Andersen MN, Vallet C, Mujezinovic A, Haunsø S, Svendsen JH, Olesen SP, Olesen MS, Schmitt N. Steffensen AB, et al. Among authors: schmitt n. J Cardiovasc Electrophysiol. 2015 Jul;26(7):715-23. doi: 10.1111/jce.12666. Epub 2015 May 4. J Cardiovasc Electrophysiol. 2015. PMID: 25786344

2

KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval.

Lundby A, Ravn LS, Svendsen JH, Olesen SP, Schmitt N. Lundby A, et al. Among authors: schmitt n. Heart Rhythm. 2007 Dec;4(12):1532-41. doi: 10.1016/j.hrthm.2007.07.022. Epub 2007 Aug 1. Heart Rhythm. 2007. PMID: 17997361

3

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation.

Lundby A, Ravn LS, Svendsen JH, Hauns S, Olesen SP, Schmitt N. Lundby A, et al. Among authors: schmitt n. Cell Physiol Biochem. 2008;21(1-3):47-54. doi: 10.1159/000113746. Epub 2008 Jan 16. Cell Physiol Biochem. 2008. PMID: 18209471

4

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.

Olesen MS, Jespersen T, Nielsen JB, Liang B, Møller DV, Hedley P, Christiansen M, Varró A, Olesen SP, Haunsø S, Schmitt N, Svendsen JH. Olesen MS, et al. Among authors: schmitt n. Cardiovasc Res. 2011 Mar 1;89(4):786-93. doi: 10.1093/cvr/cvq348. Epub 2010 Nov 4. Cardiovasc Res. 2011. PMID: 21051419

5

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.

Olesen MS, Bentzen BH, Nielsen JB, Steffensen AB, David JP, Jabbari J, Jensen HK, Haunsø S, Svendsen JH, Schmitt N. Olesen MS, et al. Among authors: schmitt n. BMC Med Genet. 2012 Apr 3;13:24. doi: 10.1186/1471-2350-13-24. BMC Med Genet. 2012. PMID: 22471742 Free PMC article.

6

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.

Olesen MS, Yuan L, Liang B, Holst AG, Nielsen N, Nielsen JB, Hedley PL, Christiansen M, Olesen SP, Haunsø S, Schmitt N, Jespersen T, Svendsen JH. Olesen MS, et al. Among authors: schmitt n. Circ Cardiovasc Genet. 2012 Aug 1;5(4):450-9. doi: 10.1161/CIRCGENETICS.111.962597. Epub 2012 Jun 8. Circ Cardiovasc Genet. 2012. PMID: 22685113

7

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.

Christophersen IE, Olesen MS, Liang B, Andersen MN, Larsen AP, Nielsen JB, Haunsø S, Olesen SP, Tveit A, Svendsen JH, Schmitt N. Christophersen IE, et al. Among authors: schmitt n. Eur Heart J. 2013 May;34(20):1517-25. doi: 10.1093/eurheartj/ehs442. Epub 2012 Dec 21. Eur Heart J. 2013. PMID: 23264583

8

Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization.

David JP, Andersen MN, Olesen SP, Rasmussen HB, Schmitt N. David JP, et al. Among authors: schmitt n. Traffic. 2013 Apr;14(4):399-411. doi: 10.1111/tra.12042. Epub 2013 Feb 13. Traffic. 2013. PMID: 23324056 Free article.

9

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.

Olesen MS, Refsgaard L, Holst AG, Larsen AP, Grubb S, Haunsø S, Svendsen JH, Olesen SP, Schmitt N, Calloe K. Olesen MS, et al. Among authors: schmitt n. Cardiovasc Res. 2013 Jun 1;98(3):488-95. doi: 10.1093/cvr/cvt028. Epub 2013 Feb 11. Cardiovasc Res. 2013. PMID: 23400760

10

Genetic modifier of the QTc interval associated with early-onset atrial fibrillation.

Andreasen L, Nielsen JB, Christophersen IE, Holst AG, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS. Andreasen L, et al. Among authors: schmitt n. Can J Cardiol. 2013 Oct;29(10):1234-40. doi: 10.1016/j.cjca.2013.06.009. Can J Cardiol. 2013. PMID: 24074973

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