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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: karkkainen st. Radiology. 2008 Oct;249(1):88-96. doi: 10.1148/radiol.2491071584. Radiology. 2008. PMID: 18796670
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland.
Jääskeläinen P, Kuusisto J, Miettinen R, Kärkkäinen P, Kärkkäinen S, Heikkinen S, Peltola P, Pihlajamäki J, Vauhkonen I, Laakso M. Jääskeläinen P, et al. Among authors: karkkainen p, karkkainen s. J Mol Med (Berl). 2002 Jul;80(7):412-22. doi: 10.1007/s00109-002-0323-9. Epub 2002 Apr 11. J Mol Med (Berl). 2002. PMID: 12110947
Genetics of dilated cardiomyopathy.
Kärkkäinen S, Peuhkurinen K. Kärkkäinen S, et al. Ann Med. 2007;39(2):91-107. doi: 10.1080/07853890601145821. Ann Med. 2007. PMID: 17453673 Free article. Review.
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: karkkainen s. 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: karkkainen s. 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.
81 results