Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Krzysztof Weroński"'
Autor:
Mirosław Kowalski, Mateusz Śpiewak, Krzysztof Weroński, Witold Rużyłło, Urszula Kozicka, Ewa Piotrowicz, Marcin Demkow, Piotr Hoffman, Hanna Siudalska, Elżbieta Katarzyna Biernacka
Publikováno v:
The Canadian journal of cardiology. 33(12)
Transcatheter pulmonary valve implantation (TPVI) is a relatively new method of treating patients with significant pulmonary regurgitation or pulmonary stenosis, or both, after reconstruction of the right ventricular outflow tract. It is an attractiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d492e0290e5782ed51a9c8fb54e86fdc
https://pubmed.ncbi.nlm.nih.gov/29173614
https://pubmed.ncbi.nlm.nih.gov/29173614
Autor:
Mirosław Kowalski, Mateusz Śpiewak, Ewa Piotrowicz, Aneta Fronczak, Marcin Demkow, Witold Rużyłło, Magdalena Mazgaj, Piotr Hoffman, Krzysztof Weroński, Ryszard Piotrowicz, Elżbieta Katarzyna Biernacka
Publikováno v:
Cardiology journal. 22(3)
Background: The aim of the study was to evaluate the role of cardiopulmonary exercise testing (CPET) parameters in assessing exercise capacity improvement after percutaneous pulmonary valve implantation (PPVI). Additionally, it aimed to determine if
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa76cae318e3d4c42498fcb4c4ea10eb
https://pubmed.ncbi.nlm.nih.gov/25733320
https://pubmed.ncbi.nlm.nih.gov/25733320
Publikováno v:
Journal of Rare Cardiovascular Diseases. 1
A 21 year old woman with phenylketonuria, positive hepatitis B surface antigen and anomalous left coronary artery originating from the pulmonary artery (ALCAPA) was referred to our clinic to asses her current condition and to establish her further tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2f63cbfb786b28a986138d7a7ba2855
https://doi.org/10.20418/jrcd.vol1no5.19
https://doi.org/10.20418/jrcd.vol1no5.19
Publikováno v:
Kardiologia polska. 68(11)
Isolated left ventricular noncompaction is a primary, genetic cardiomyopathy thought to be caused by arrest of normal embryogenesis of endocardium and myocardium, characterised by a pattern of excessively prominent trabecular meshwork and deep intert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8228041ef7b89ff98186905fdb95f136
https://pubmed.ncbi.nlm.nih.gov/21108206
https://pubmed.ncbi.nlm.nih.gov/21108206