Satu Kärkkäinen

Summary

Affiliation: Kuopio University Hospital
Country: Finland

Publications

  1. ncbi request reprint Genetics of dilated cardiomyopathy
    Satu Kärkkäinen
    Kuopio University and Kuopio University Hospital, Kuopio, Finland
    Ann Med 39:91-107. 2007
  2. doi request reprint Idiopathic dilated cardiomyopathy and chronic atrial fibrillation
    Petri O Tuomainen
    Department of Internal Medicine, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland Heart Center, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland
    Clin Physiol Funct Imaging 34:133-7. 2014
  3. ncbi request reprint A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy
    Satu Kärkkäinen
    Department of Medicine, University of Kuopio, P O Box 1777, Kuopio, Finland
    Eur Heart J 25:885-93. 2004

Collaborators

Detail Information

Publications3

  1. ncbi request reprint Genetics of dilated cardiomyopathy
    Satu Kärkkäinen
    Kuopio University and Kuopio University Hospital, Kuopio, Finland
    Ann Med 39:91-107. 2007
    ..This review deals with DCM of genetic origin...
  2. doi request reprint Idiopathic dilated cardiomyopathy and chronic atrial fibrillation
    Petri O Tuomainen
    Department of Internal Medicine, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland Heart Center, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland
    Clin Physiol Funct Imaging 34:133-7. 2014
    ..Atrial fibrillation (AF) is common in idiopathic dilated cardiomyopathy (IDC). We explored the clinical characteristics of IDC patients with chronic AF compared with those with sinus rhythm (SR)...
  3. ncbi request reprint A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy
    Satu Kärkkäinen
    Department of Medicine, University of Kuopio, P O Box 1777, Kuopio, Finland
    Eur Heart J 25:885-93. 2004
    ..The mutations most frequently associated with dilated cardiomyopathy (DCM) have been reported in the lamin A/C gene. The role of variants of the lamin A/C gene was investigated in patients with DCM from eastern and southern Finland...