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International Journal of Legal Medicine
|
July 23, 2011
Differences in investigations of sudden unexpected deaths in young people in a nationwide setting
Bo Gregers Winkel, Anders Gaarsdal Holst, Juliane Theilade, et al.
European Heart Journal
|
December 7, 2010
Nationwide study of sudden cardiac death in persons aged 1-35 years
Bo Gregers Winkel, Anders Gaarsdal Holst, Juliane Theilade, et al.
Cardiology
|
August 24, 2013
Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome
Juliane Theilade, Jørgen Kanters, Finn Lund Henriksen, et al.
European Heart Journal
|
May 13, 2019
Long-term proarrhythmic pharmacotherapy among patients with congenital long QT syndrome and risk of arrhythmia and mortality
Peter E Weeke, Jesper S Kellemann, Camilla Bang Jespersen, et al.
BMC Medical Genetics
|
March 11, 2014
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2
Michael Christiansen, Paula L Hedley, Juliane Theilade, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
International Journal of Legal Medicine
|
July 23, 2011
Differences in investigations of sudden unexpected deaths in young people in a nationwide setting
Bo Gregers Winkel, Anders Gaarsdal Holst, Juliane Theilade, et al.
European Heart Journal
|
December 7, 2010
Nationwide study of sudden cardiac death in persons aged 1-35 years
Bo Gregers Winkel, Anders Gaarsdal Holst, Juliane Theilade, et al.
Cardiology
|
August 24, 2013
Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome
Juliane Theilade, Jørgen Kanters, Finn Lund Henriksen, et al.
European Heart Journal
|
May 13, 2019
Long-term proarrhythmic pharmacotherapy among patients with congenital long QT syndrome and risk of arrhythmia and mortality
Peter E Weeke, Jesper S Kellemann, Camilla Bang Jespersen, et al.
BMC Medical Genetics
|
March 11, 2014
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2
Michael Christiansen, Paula L Hedley, Juliane Theilade, et al.
Page
of 3