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Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
Kärkkäinen S, Heliö T, Jääskeläinen P, Miettinen R, Tuomainen P, Ylitalo K, Kaartinen M, Reissell E, Toivonen L, Nieminen MS, Kuusisto J, Laakso M, Peuhkurinen K. Kärkkäinen S, et al. Among authors: kaartinen m. Eur J Heart Fail. 2004 Dec;6(7):861-8. doi: 10.1016/j.ejheart.2004.04.017. Eur J Heart Fail. 2004. PMID: 15556047 Free article.
Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data.
Koikkalainen JR, Antila M, Lötjönen JM, Heliö T, Lauerma K, Kivistö SM, Sipola P, Kaartinen MA, Kärkkäinen ST, Reissell E, Kuusisto J, Laakso M, Oresic M, Nieminen MS, Peuhkurinen KJ. Koikkalainen JR, et al. Among authors: kaartinen ma. Radiology. 2008 Oct;249(1):88-96. doi: 10.1148/radiol.2491071584. Radiology. 2008. PMID: 18796670
Pregnancy and childbirth in carriers of the lamin A/C-gene mutation.
Palojoki E, Kaartinen M, Kaaja R, Reissell E, Kärkkäinen S, Kuusisto J, Heliö T. Palojoki E, et al. Among authors: kaartinen m. Eur J Heart Fail. 2010 Jun;12(6):630-3. doi: 10.1093/eurjhf/hfq059. Epub 2010 Apr 22. Eur J Heart Fail. 2010. PMID: 20413395 Free article.
Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy.
Holmström M, Kivistö S, Heliö T, Jurkko R, Kaartinen M, Antila M, Reissell E, Kuusisto J, Kärkkäinen S, Peuhkurinen K, Koikkalainen J, Lötjönen J, Lauerma K. Holmström M, et al. Among authors: kaartinen m. J Cardiovasc Magn Reson. 2011 Jun 20;13(1):30. doi: 10.1186/1532-429X-13-30. J Cardiovasc Magn Reson. 2011. PMID: 21689390 Free PMC article.
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population.
Jääskeläinen P, Heliö T, Aalto-Setälä K, Kaartinen M, Ilveskoski E, Hämäläinen L, Melin J, Nieminen MS, Laakso M, Kuusisto J; FinHCM study group; Kervinen H, Mustonen J, Juvonen J, Niemi M, Uusimaa P, Huttunen M, Kotila M, Pietilä M. Jääskeläinen P, et al. Among authors: kaartinen m. Ann Med. 2013 Feb;45(1):85-90. doi: 10.3109/07853890.2012.671534. Epub 2012 Apr 2. Ann Med. 2013. PMID: 22462493 Free article.
A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy.
Jääskeläinen P, Heliö T, Aalto-Setälä K, Kaartinen M, Ilveskoski E, Hämäläinen L, Melin J, Kärkkäinen S, Peuhkurinen K, Nieminen MS, Laakso M; FinHCM Study Group; Kuusisto J. Jääskeläinen P, et al. Among authors: kaartinen m. Ann Med. 2014 Sep;46(6):424-9. doi: 10.3109/07853890.2014.912834. Epub 2014 Jun 3. Ann Med. 2014. PMID: 24888384 Free article.
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.
Akinrinade O, Ollila L, Vattulainen S, Tallila J, Gentile M, Salmenperä P, Koillinen H, Kaartinen M, Nieminen MS, Myllykangas S, Alastalo TP, Koskenvuo JW, Heliö T. Akinrinade O, et al. Among authors: kaartinen m. Eur Heart J. 2015 Sep 7;36(34):2327-37. doi: 10.1093/eurheartj/ehv253. Epub 2015 Jun 17. Eur Heart J. 2015. PMID: 26084686 Free PMC article.
172 results