Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kathleen E. Erskine"'
Autor:
Thomas V. McDonald, Marina Stolerman, Lilian L. Cohen, Robert W. Marion, Esma Paljevic, David H. Wasserman, Nicole DeGroat, Eleanor Griffith, Siobhan M. Dolan, Christine A. Walsh, Nadia Hidayatallah, Louise Bordeaux Silverstein, Kathleen E. Erskine
Publikováno v:
Personalized Medicine. 10:73-80
In the genomic age, the challenges presented by various inherited conditions present a compelling argument for an interdisciplinary model of care. Cardiac arrhythmias with a genetic basis, such as long QT syndrome, require clinicians with expertise i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6296728311daae1087a1fd9bfd1efcfe
https://doi.org/10.2217/pme.12.108
https://doi.org/10.2217/pme.12.108
Autor:
Robert W. Marion, Christine A. Walsh, Siobhan M. Dolan, Kathleen E. Erskine, Nadia Hidayatallah, Thomas V. McDonald, Lilian L. Cohen
Genetic testing is becoming increasingly available for cardiac channelopathies, such as long QT syndrome and Brugada syndrome, which can lead to sudden cardiac death. Test results can be used to shape an individual’s medical management and to ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81169757f855cbb519117bf38520a212
https://europepmc.org/articles/PMC4157088/
https://europepmc.org/articles/PMC4157088/
Publikováno v:
AJOB primary research. 3(3)
BACKGROUND: With current genetic technology, it is possible to detect mutations associated with long QT syndrome (LQTS), a hereditary cardiac arrhythmia syndrome. As a result, prospective parents diagnosed with LQTS will have to decide whether or not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4291c4157d81a188e99b55d02fd2d89b
https://pubmed.ncbi.nlm.nih.gov/22822470
https://pubmed.ncbi.nlm.nih.gov/22822470