Kontula K - Search Results

1

Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in Finland.

Kaartinen M, Heliö T, Lehtonen A, Lahtinen AM, Kärkkäinen S, Keto P, Kontula K, Toivonen L. Kaartinen M, et al. Among authors: kontula k. Ann Med. 2007;39(4):312-8. doi: 10.1080/07853890701282003. Ann Med. 2007. PMID: 17558603 Free article.

2

Plakophilin-2 missense mutations in arrhythmogenic right ventricular cardiomyopathy.

Lahtinen AM, Lehtonen A, Kaartinen M, Toivonen L, Swan H, Widén E, Lehtonen E, Lehto VP, Kontula K. Lahtinen AM, et al. Among authors: kontula k. Int J Cardiol. 2008 May 7;126(1):92-100. doi: 10.1016/j.ijcard.2007.03.137. Epub 2007 May 22. Int J Cardiol. 2008. PMID: 17521752

3

Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy.

Lahtinen AM, Lehtonen E, Marjamaa A, Kaartinen M, Heliö T, Porthan K, Oikarinen L, Toivonen L, Swan H, Jula A, Peltonen L, Palotie A, Salomaa V, Kontula K. Lahtinen AM, et al. Among authors: kontula k. Heart Rhythm. 2011 Aug;8(8):1214-21. doi: 10.1016/j.hrthm.2011.03.015. Epub 2011 Mar 10. Heart Rhythm. 2011. PMID: 21397041

4

Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland.

Fodstad H, Swan H, Laitinen P, Piippo K, Paavonen K, Viitasalo M, Toivonen L, Kontula K. Fodstad H, et al. Among authors: kontula k. Ann Med. 2004;36 Suppl 1:53-63. doi: 10.1080/17431380410032689. Ann Med. 2004. PMID: 15176425 Free article.

5

Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia.

Laitinen PJ, Swan H, Piippo K, Viitasalo M, Toivonen L, Kontula K. Laitinen PJ, et al. Among authors: kontula k. Ann Med. 2004;36 Suppl 1:81-6. doi: 10.1080/17431380410032599. Ann Med. 2004. PMID: 15176428 Free article. Review.

6

High prevalence of four long QT syndrome founder mutations in the Finnish population.

Marjamaa A, Salomaa V, Newton-Cheh C, Porthan K, Reunanen A, Karanko H, Jula A, Lahermo P, Väänänen H, Toivonen L, Swan H, Viitasalo M, Nieminen MS, Peltonen L, Oikarinen L, Palotie A, Kontula K. Marjamaa A, et al. Among authors: kontula k. Ann Med. 2009;41(3):234-40. doi: 10.1080/07853890802668530. Ann Med. 2009. PMID: 19160088 Free PMC article.

7

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia.

Marjamaa A, Laitinen-Forsblom P, Lahtinen AM, Viitasalo M, Toivonen L, Kontula K, Swan H. Marjamaa A, et al. Among authors: kontula k. BMC Med Genet. 2009 Feb 12;10:12. doi: 10.1186/1471-2350-10-12. BMC Med Genet. 2009. PMID: 19216760 Free PMC article.

8

Depressive symptoms in the congenital long QT syndrome.

Hintsa T, Keltikangas-Järvinen L, Puttonen S, Ravaja N, Toivonen L, Kontula K, Swan H. Hintsa T, et al. Among authors: kontula k. Ann Med. 2009;41(7):516-21. doi: 10.1080/07853890903037254. Ann Med. 2009. PMID: 19551538 Free article.

9

Intravenous epinephrine infusion test in diagnosis of catecholaminergic polymorphic ventricular tachycardia.

Marjamaa A, Hiippala A, Arrhenius B, Lahtinen AM, Kontula K, Toivonen L, Happonen JM, Swan H. Marjamaa A, et al. Among authors: kontula k. J Cardiovasc Electrophysiol. 2012 Feb;23(2):194-9. doi: 10.1111/j.1540-8167.2011.02188.x. Epub 2011 Sep 28. J Cardiovasc Electrophysiol. 2012. PMID: 21954897

10

Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.

Lahtinen AM, Havulinna AS, Noseworthy PA, Jula A, Karhunen PJ, Perola M, Newton-Cheh C, Salomaa V, Kontula K. Lahtinen AM, et al. Among authors: kontula k. Ann Med. 2013 Jun;45(4):328-35. doi: 10.3109/07853890.2013.783995. Epub 2013 May 8. Ann Med. 2013. PMID: 23651034 Free PMC article.

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