Christiansen M - Search Results

1

Family history of premature death and risk of early onset cardiovascular disease.

Ranthe MF, Carstensen L, Oyen N, Tfelt-Hansen J, Christiansen M, McKenna WJ, Wohlfahrt J, Melbye M, Boyd HA. Ranthe MF, et al. Among authors: christiansen m. J Am Coll Cardiol. 2012 Aug 28;60(9):814-21. doi: 10.1016/j.jacc.2012.06.018. J Am Coll Cardiol. 2012. PMID: 22917005 Free article.

2

The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.

Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Havndrup O, et al. Among authors: christiansen m. Am J Cardiol. 2001 Jun 1;87(11):1315-7. doi: 10.1016/s0002-9149(01)01532-6. Am J Cardiol. 2001. PMID: 11377367 No abstract available.

3

Predictors of coronary in-stent restenosis: importance of angiotensin-converting enzyme gene polymorphism and treatment with angiotensin-converting enzyme inhibitors.

Jørgensen E, Kelbaek H, Helqvist S, Jensen GV, Saunamäki K, Kastrup J, Havndrup O, Bundgaard H, Kyst Madsen J, Christiansen M, Andersen PS, Reiber JH. Jørgensen E, et al. Among authors: christiansen m. J Am Coll Cardiol. 2001 Nov 1;38(5):1434-9. doi: 10.1016/s0735-1097(01)01580-7. J Am Coll Cardiol. 2001. PMID: 11691520 Free article.

4

Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.

Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K. Christiansen M, et al. Am J Cardiol. 2005 Feb 1;95(3):433-4. doi: 10.1016/j.amjcard.2004.09.054. Am J Cardiol. 2005. PMID: 15670565

5

[Dynamic ECG changes as a result of Brugada syndrome, an overlooked diagnosis?].

Tfelt-Hansen J, Svendsen JH, Hofman-Bang J, Amtorp O, Christiansen M, Haunsø S. Tfelt-Hansen J, et al. Among authors: christiansen m. Ugeskr Laeger. 2005 Aug 15;167(33):3060-1. Ugeskr Laeger. 2005. PMID: 16109254 Danish.

6

Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.

Grunnet M, Behr ER, Calloe K, Hofman-Bang J, Till J, Christiansen M, McKenna WJ, Olesen SP, Schmitt N. Grunnet M, et al. Among authors: christiansen m. Heart Rhythm. 2005 Nov;2(11):1238-49. doi: 10.1016/j.hrthm.2005.07.025. Heart Rhythm. 2005. PMID: 16253915

7

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.

Hofman-Bang J, Behr ER, Hedley P, Tfelt-Hansen J, Kanters JK, Haunsøe S, McKenna WJ, Christiansen M. Hofman-Bang J, et al. Among authors: christiansen m. Clin Genet. 2006 Jun;69(6):504-11. doi: 10.1111/j.1399-0004.2006.00621.x. Clin Genet. 2006. PMID: 16712702

8

The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome.

Nyberg MT, Stoevring B, Behr ER, Ravn LS, McKenna WJ, Christiansen M. Nyberg MT, et al. Among authors: christiansen m. Clin Chim Acta. 2007 Jan;375(1-2):87-91. doi: 10.1016/j.cca.2006.06.020. Epub 2006 Jun 22. Clin Chim Acta. 2007. PMID: 17010328

9

Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations.

Frank-Hansen R, Page SP, Syrris P, McKenna WJ, Christiansen M, Andersen PS. Frank-Hansen R, et al. Among authors: christiansen m. Eur J Hum Genet. 2008 Sep;16(9):1062-9. doi: 10.1038/ejhg.2008.52. Epub 2008 Mar 12. Eur J Hum Genet. 2008. PMID: 18337725

10

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

Behr ER, Dalageorgou C, Christiansen M, Syrris P, Hughes S, Tome Esteban MT, Rowland E, Jeffery S, McKenna WJ. Behr ER, et al. Among authors: christiansen m. Eur Heart J. 2008 Jul;29(13):1670-80. doi: 10.1093/eurheartj/ehn219. Epub 2008 May 27. Eur Heart J. 2008. PMID: 18508782

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