Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christina-Maria Kotta"'
Autor:
J. Papagiannis, Kostas Gatzoulis, Aris Anastasakis, P. Geleris, Christina-Maria Kotta, Christodoulos Stefanadis
Publikováno v:
Journal of Applied Genetics. 51:515-518
The long QT syndrome (LQTS) is an inherited cardiac arrhythmia that may lead to sudden death in the absence of structural heart disease. Mutations in the cardiac potassium and sodium channel genes can be found in approximately 70 percent of patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ee52af61f990484b5dcb8d863bb56b9
https://doi.org/10.1007/bf03208882
https://doi.org/10.1007/bf03208882
Autor:
Christina-Maria Kotta, Aris Anastasakis, Christodoulos Stefanadis, Antonis S. Manolis, Konstantinos Gatzoulis
Publikováno v:
International Journal of Cardiology. 145:45-48
Brugada syndrome (BrS) is an inherited cardiac arrhythmia that may lead to sudden death in patients with structurally normal heart. Mutations in the alpha subunit of the cardiac sodium channel SCN5A gene are found in approximately 20% of cases. We cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d640a86d8d0a69777a21945762d36b2
https://doi.org/10.1016/j.ijcard.2009.03.134
https://doi.org/10.1016/j.ijcard.2009.03.134
Publikováno v:
Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese. 53(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0aa4d40824948b7209119466c4367dbd
https://pubmed.ncbi.nlm.nih.gov/23178427
https://pubmed.ncbi.nlm.nih.gov/23178427
Autor:
Stavros Kyriakogonas, Christina-Maria Kotta, Artemisia Theopistou, Christodoulos Stefanadis, Aris Anastasakis, Bernd Wollnik
Publikováno v:
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology. 8(4)
We aimed to verify the long QT syndrome (LQTS) genotype in a family with strong evidence of LQTS type 1 (LQT1) on the basis of so far established genotype–phenotype correlations. Genetic testing for mutations in the KCNQ1 potassium channel gene rev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a877e0f55c06f690818705b7a6e2900f
https://pubmed.ncbi.nlm.nih.gov/16627448
https://pubmed.ncbi.nlm.nih.gov/16627448