Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Prodromos Azariadis"'
OC21 - Psychosocial functioning of parents of infants diagnosed with complex congenital heart defect
Autor:
Ioanna Voutoufianaki, Anna Manatou, Konstantinos Petsios, Vassiliki Matziou, Spiros Rammos, Prodromos Azariadis
Publikováno v:
Nursing children and young people. 28(4)
UNLABELLED Theme: Parenting/parenthood. INTRODUCTION The diagnosis of complex CHD impacts the psychosocial status of parents and their functioning. PURPOSE A critical evaluation of the literature concerning the psychosocial parental response to their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::327263b870fec91ec6e157827f3c960c
https://pubmed.ncbi.nlm.nih.gov/27214437
https://pubmed.ncbi.nlm.nih.gov/27214437
Autor:
Spyridon Rammos, Constantinos Contrafouris, Meletios A. Kanakis, Christos Apostolidis, Andrew C. Chatzis, Cleo Laskari, Fotios Mitropoulos, Prodromos Azariadis
Publikováno v:
Cardiovascular Journal Of Africa. 25:e1-e3
The case is presented of a previously healthy infant with a known asymptomatic bicuspid aortic valve who developed fungal endocarditis. The patient underwent aortic root replacement with a pulmonary autograft (Ross procedure). Cultured operative mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fec75a02f94c6d83c3f346724d48f9e3
https://doi.org/10.5830/cvja-2014-031
https://doi.org/10.5830/cvja-2014-031
Autor:
Michael Milonakis, Prodromos Azariadis, Andrew C. Chatzis, Meletios A. Kanakis, Constantinos Contrafouris
Publikováno v:
Clinical Case Reports
Key Clinical Message A 42‐year‐old woman was diagnosed during the 3rd month of pregnancy with a large right atrial tumor. Three weeks after successful completion of a full‐term pregnancy, she was admitted and underwent surgical removal of the t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291e6a01cd6814015bcf2331a3d79f8a
https://doi.org/10.1002/ccr3.691
https://doi.org/10.1002/ccr3.691
Publikováno v:
Asian cardiovascularthoracic annals. 23(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8f10880d575d244b5df5a29a49bf9cd
https://pubmed.ncbi.nlm.nih.gov/24585308
https://pubmed.ncbi.nlm.nih.gov/24585308
Autor:
Prodromos Azariadis, Fotios Mitropoulos, Constantinos Contrafouris, Meletios A. Kanakis, Andrew C. Chatzis
Publikováno v:
Case Reports in Surgery
Case Reports in Surgery, Vol 2014 (2014)
Case Reports in Surgery, Vol 2014 (2014)
Supravalvar aortic stenosis (SVAS) in patients with Williams’ syndrome is often accompanied by coronary, pulmonary, and even myocardial lesions and therefore associated with increased perioperative morbidity and mortality. Extracorporeal membrane o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::258f0f5a5005068fce1cc636974c144e
http://europepmc.org/articles/PMC3972828
http://europepmc.org/articles/PMC3972828
Autor:
Meletios A. Kanakis, Nicholaos Giannopoulos, Fotios Mitropoulos, Constantinos Contrafouris, Alexander Tsoutsinos, Michael Milonakis, Prodromos Azariadis, Andrew C. Chatzis
Publikováno v:
Journal of Cardiothoracic Surgery
Results There were no deaths. Median ICU and hospital stay were 5 and 11 days respectively. Median postoperative (discharge) PV peak gradient (PG) was 23mmHg, median pulmonary regurgitation (PR) 2+/4+ and median tricuspid regurgitation (TR) 1+/4+. Te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::111e42a039abfafd6f8d49e8c234ad97
https://doi.org/10.1186/1749-8090-8-s1-o311
https://doi.org/10.1186/1749-8090-8-s1-o311
Autor:
Fotios A, Mitropoulos, Meletios A, Kanakis, Constantinos, Contrafouris, Cleo, Laskari, Spyridon, Rammos, Christos, Apostolidis, Prodromos, Azariadis, Andrew C, Chatzis
Publikováno v:
Cardiovascular journal of Africa. 25(4)
The case is presented of a previously healthy infant with a known asymptomatic bicuspid aortic valve who developed fungal endocarditis. The patient underwent aortic root replacement with a pulmonary autograft (Ross procedure). Cultured operative mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec933dc903cc4dc3d81edf0d772f090c
https://pubmed.ncbi.nlm.nih.gov/25192408
https://pubmed.ncbi.nlm.nih.gov/25192408
Autor:
Theofili Kousi, Andrew C. Chatzis, Prodromos Azariadis, Vassiliki Fotiadou, Cleo Laskari, Gregory Chryssostomidis, Meletios A. Kanakis, Christos Apostolidis
Publikováno v:
International Journal of Surgery Case Reports
INTRODUCTION The Holt–Oram syndrome is a rare congenital disorder involving the skeletal and cardiovascular systems. It is characterized by upper limb deformities and cardiac malformations, atrial septal defects in particular. PRESENTATION OF CASE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0370757330edc448987c00072610c08