Lahtinen AM - 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: lahtinen am. 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. 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. 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

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: lahtinen am. BMC Med Genet. 2009 Feb 12;10:12. doi: 10.1186/1471-2350-10-12. BMC Med Genet. 2009. PMID: 19216760 Free PMC article.

5

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. 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.

6

Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain-of-Function Mutation in the Nav 1.5 Sodium Channel.

Amarouch MY, Swan H, Leinonen J, Marjamaa A, Lahtinen AM, Kontula K, Toivonen L, Widen E, Abriel H. Amarouch MY, et al. Among authors: lahtinen am. Ann Noninvasive Electrocardiol. 2016 Jul;21(4):343-51. doi: 10.1111/anec.12312. Epub 2015 Oct 7. Ann Noninvasive Electrocardiol. 2016. PMID: 26965448 Free PMC article.

7

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: lahtinen am. 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

8

Gain-of-function mutation of the SCN5A gene causes exercise-induced polymorphic ventricular arrhythmias.

Swan H, Amarouch MY, Leinonen J, Marjamaa A, Kucera JP, Laitinen-Forsblom PJ, Lahtinen AM, Palotie A, Kontula K, Toivonen L, Abriel H, Widen E. Swan H, et al. Among authors: lahtinen am. Circ Cardiovasc Genet. 2014 Dec;7(6):771-81. doi: 10.1161/CIRCGENETICS.114.000703. Epub 2014 Sep 10. Circ Cardiovasc Genet. 2014. PMID: 25210054 Free article.

9

Prevalence and clinical correlates of familial hypercholesterolemia founder mutations in the general population.

Lahtinen AM, Havulinna AS, Jula A, Salomaa V, Kontula K. Lahtinen AM, et al. Atherosclerosis. 2015 Jan;238(1):64-9. doi: 10.1016/j.atherosclerosis.2014.11.015. Epub 2014 Nov 18. Atherosclerosis. 2015. PMID: 25437892

10

Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.

Koponen M, Marjamaa A, Hiippala A, Happonen JM, Havulinna AS, Salomaa V, Lahtinen AM, Hintsa T, Viitasalo M, Toivonen L, Kontula K, Swan H. Koponen M, et al. Among authors: lahtinen am. Circ Arrhythm Electrophysiol. 2015 Aug;8(4):815-23. doi: 10.1161/CIRCEP.114.002654. Epub 2015 Jun 10. Circ Arrhythm Electrophysiol. 2015. PMID: 26063740

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