Olesen MS - Search Results

1

Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis.

Liang B, Soka M, Christensen AH, Olesen MS, Larsen AP, Knop FK, Wang F, Nielsen JB, Andersen MN, Humphreys D, Mann SA, Huttner IG, Vandenberg JI, Svendsen JH, Haunsø S, Preiss T, Seebohm G, Olesen SP, Schmitt N, Fatkin D. Liang B, et al. Among authors: olesen sp, olesen ms. J Mol Cell Cardiol. 2014 Feb;67:69-76. doi: 10.1016/j.yjmcc.2013.12.014. Epub 2013 Dec 27. J Mol Cell Cardiol. 2014. PMID: 24374141

2

Single nucleotide polymorphisms in inflammatory genes and the risk of early onset of lone atrial fibrillation.

Henningsen KM, Olesen MS, Pedersen M, Nielsen L, Haunsø S, Bruunsgaard H, Svendsen JH. Henningsen KM, et al. Among authors: olesen ms. Inflamm Res. 2010 Nov;59(11):965-9. doi: 10.1007/s00011-010-0210-8. Epub 2010 May 20. Inflamm Res. 2010. PMID: 20490891

3

[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease].

Holst AG, Tfelt-Hansen J, Olesen MS, Theilade J, Winkel BG, Christensen AH, Bundgaard H, Haunsø S, Svendsen JH. Holst AG, et al. Among authors: olesen ms. Ugeskr Laeger. 2010 Aug 2;172(31):2140-4. Ugeskr Laeger. 2010. PMID: 20670590 Review. Danish.

4

Abnormal atrial activation in young patients with lone atrial fibrillation.

Holmqvist F, Olesen MS, Tveit A, Enger S, Tapanainen J, Jurkko R, Havmöller R, Haunsø S, Carlson J, Svendsen JH, Platonov PG. Holmqvist F, et al. Among authors: olesen ms. Europace. 2011 Feb;13(2):188-92. doi: 10.1093/europace/euq352. Epub 2010 Sep 23. Europace. 2011. PMID: 20864492

5

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: olesen sp. Cardiovasc Res. 2011 Mar 1;89(4):786-93. doi: 10.1093/cvr/cvq348. Epub 2010 Nov 4. Cardiovasc Res. 2011. PMID: 21051419

6

Inflammatory single nucleotide polymorphisms and the risk of atrial fibrillation: a case control study.

Henningsen KM, Olesen MS, Ravn LS, Dixen U, Haunsoe S, Bruunsgaard H, Svendsen JH. Henningsen KM, et al. Among authors: olesen ms. Inflamm Res. 2011 Mar;60(3):209-11. doi: 10.1007/s00011-010-0285-2. Epub 2010 Dec 4. Inflamm Res. 2011. PMID: 21132345

7

Incomplete right bundle branch block: a novel electrocardiographic marker for lone atrial fibrillation.

Nielsen JB, Olesen MS, Tangø M, Haunsø S, Holst AG, Svendsen JH. Nielsen JB, et al. Among authors: olesen ms. Europace. 2011 Feb;13(2):182-7. doi: 10.1093/europace/euq436. Epub 2010 Dec 7. Europace. 2011. PMID: 21138928

8

[Short QT syndrome as an inherited condition].

Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Møller DV, et al. Ugeskr Laeger. 2011 Feb 7;173(6):420-4. Ugeskr Laeger. 2011. PMID: 21299935 Review. Danish.

9

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis.

Winkel BG, Hollegaard MV, Olesen MS, Svendsen JH, Haunsø S, Hougaard DM, Tfelt-Hansen J. Winkel BG, et al. Among authors: olesen ms. BMC Med Genet. 2011 Feb 9;12:22. doi: 10.1186/1471-2350-12-22. BMC Med Genet. 2011. PMID: 21306642 Free PMC article.

10

Screening of KCNN3 in patients with early-onset lone atrial fibrillation.

Olesen MS, Jabbari J, Holst AG, Nielsen JB, Steinbrüchel DA, Jespersen T, Haunsø S, Svendsen JH. Olesen MS, et al. Europace. 2011 Jul;13(7):963-7. doi: 10.1093/europace/eur007. Epub 2011 Mar 11. Europace. 2011. PMID: 21398315

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