Kontula K - Search Results

1

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.

2

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.

Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ. Marks AR, et al. Among authors: kontula k. J Cell Physiol. 2002 Jan;190(1):1-6. doi: 10.1002/jcp.10031. J Cell Physiol. 2002. PMID: 11807805 Review.

3

Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms.

Laitinen PJ, Swan H, Kontula K. Laitinen PJ, et al. Among authors: kontula k. Eur J Hum Genet. 2003 Nov;11(11):888-91. doi: 10.1038/sj.ejhg.5201061. Eur J Hum Genet. 2003. PMID: 14571276

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

Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak.

Lehnart SE, Wehrens XH, Laitinen PJ, Reiken SR, Deng SX, Cheng Z, Landry DW, Kontula K, Swan H, Marks AR. Lehnart SE, et al. Among authors: kontula k. Circulation. 2004 Jun 29;109(25):3208-14. doi: 10.1161/01.CIR.0000132472.98675.EC. Epub 2004 Jun 14. Circulation. 2004. PMID: 15197150

6

Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations.

Swan H, Laitinen P, Kontula K, Toivonen L. Swan H, et al. Among authors: kontula k. J Cardiovasc Electrophysiol. 2005 Feb;16(2):162-6. doi: 10.1046/j.1540-8167.2005.40516.x. J Cardiovasc Electrophysiol. 2005. PMID: 15720454

7

Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insights.

Kontula K, Laitinen PJ, Lehtonen A, Toivonen L, Viitasalo M, Swan H. Kontula K, et al. Cardiovasc Res. 2005 Aug 15;67(3):379-87. doi: 10.1016/j.cardiores.2005.04.027. Cardiovasc Res. 2005. PMID: 15913575 Review.

8

Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves.

Paavola J, Viitasalo M, Laitinen-Forsblom PJ, Pasternack M, Swan H, Tikkanen I, Toivonen L, Kontula K, Laine M. Paavola J, et al. Among authors: kontula k. Eur Heart J. 2007 May;28(9):1135-42. doi: 10.1093/eurheartj/ehl543. Epub 2007 Mar 8. Eur Heart J. 2007. PMID: 17347175

9

U-waves and T-wave peak to T-wave end intervals in patients with catecholaminergic polymorphic ventricular tachycardia, effects of beta-blockers.

Viitasalo M, Oikarinen L, Väänänen H, Kontula K, Toivonen L, Swan H. Viitasalo M, et al. Among authors: kontula k. Heart Rhythm. 2008 Oct;5(10):1382-8. doi: 10.1016/j.hrthm.2008.06.011. Epub 2008 Jun 12. Heart Rhythm. 2008. PMID: 18929323

10

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.

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