Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Morten Wagner Nielsen"'
Publikováno v:
Frontiers in Physiology, Vol 4 (2013)
Brugada Syndrome (BrS) is a clinical entity first described in 1992. BrS is characterized by ST-segment elevations in the right precordial leads and susceptibility to ventricular arrhythmias and sudden cardiac death. It affects young subjects, predom
Externí odkaz:
https://doaj.org/article/320969e6fbc842f0aa7a0317c6e30a74
Autor:
Morten Wagner Nielsen, Morten Salling Olesen, Lena eRefsgaard, Stig eHaunso, Jesper Hastrup Svendsen
Publikováno v:
Frontiers in Genetics, Vol 4 (2013)
Several studies have associated mutations in genes encoding potassium channels and accessory subunits involved in cardiac repolarisation with susceptibility of atrial fibrillation (AF). Recently, the krüppel-like factor 15 (Klf15) was found to trans
Externí odkaz:
https://doaj.org/article/7e2b6ff20c2e459eab1d74555a0d233f
Autor:
Javad Jabbari, Olesen, Jens Nielsen, Jacob Tfelt-Hansen, Anders G. Holst, Morten Wagner Nielsen, Stig Haunsø, Jesper Hastrup Svendsen, Reza Jabbari
Publikováno v:
Circulation: Cardiovascular Genetics. 6:481-489
Background— Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a lethal, rare hereditary disease with an estimated prevalence of 1:10 000. The genetic variants that cause CPVT are usually highly penetrant. To date, about 189 variants i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90667e09f9915aa59b4ea8653b2a8aca
https://doi.org/10.1161/circgenetics.113.000118
https://doi.org/10.1161/circgenetics.113.000118
Publikováno v:
European Journal of Human Genetics. 22:297-306
Atrial fibrillation (AF) is the most common cardiac arrhythmia affecting 1-2% of the general population. A number of studies have demonstrated that AF, and in particular lone AF, has a substantial genetic component. Monogenic mutations in lone and fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b25898169fde8f2f482c383dde0cde81
https://doi.org/10.1038/ejhg.2013.139
https://doi.org/10.1038/ejhg.2013.139
Autor:
Jesper Hastrup Svendsen, Lena Refsgaard, Stig Haunsø, Morten S. Olesen, Morten Wagner Nielsen
Publikováno v:
Frontiers in Genetics, Vol 4 (2013)
Frontiers in Genetics
Frontiers in Genetics
Several studies have associated mutations in genes encoding potassium channels and accessory subunits involved in cardiac repolarisation with susceptibility of atrial fibrillation (AF). Recently, the krüppel-like factor 15 (Klf15) was found to trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3aac128dc4988463b3e9002c7d43953
http://journal.frontiersin.org/Journal/10.3389/fgene.2013.00088/full
http://journal.frontiersin.org/Journal/10.3389/fgene.2013.00088/full