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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.
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.
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.
172 results