Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Changping Gan"'
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Intracardiac thrombosis (ICT) is a rare complication after the cardiopulmonary surgery for interrupted aortic arch (IAA) or total anomalous pulmonary venous connection (TAPVC) without previous records. There are still no general g
Externí odkaz:
https://doaj.org/article/38411f8b017347d081c5a34fbd3cc823
Publikováno v:
BMC Surgery, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background This report presents updated data and mid-term follow-up information to a former study introducing the novel technique of percutaneous-perventricular device closure of doubly committed subarterial ventricular septal defect. Method
Externí odkaz:
https://doaj.org/article/402c5cc7b7d4420bb39faffe93b604c9
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-5 (2020)
Abstract Introduction Marfan syndrome (MFS) is a common heritable connective tissue disease involving multiple organs. Even though the clinical manifestations of MFS can be various, aortic root aneurysm is estimated as one of the most serious complic
Externí odkaz:
https://doaj.org/article/9eb97cdbd0ee405e848001cbe846bc72
Publikováno v:
BMC Surgery, Vol 21, Iss 1, Pp 1-3 (2021)
Abstract Background Giant superior vena cava (SVC) aneurysm in non-obstructed supracardiac total anomalous pulmonary venous connection (TAPVC) is even more rare than in obstructed one, and this combination has not been reported. Case presentation Her
Externí odkaz:
https://doaj.org/article/8da2e4d9b2c04cb3806e4527b4f9d0c0
Publikováno v:
BMC Surgery, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Coronary artery aneurysms in most cases require surgical treatment once diagnosed. Lifelong anticoagulation is often needed after surgery. We herein describe a 55-year-old man who was asymptomatic and diagnosed with right giant co
Externí odkaz:
https://doaj.org/article/6ee2e182d9a143e9aecc5352b7209748
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 15, Iss 1, Pp 1-5 (2020)
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery
Introduction Marfan syndrome (MFS) is a common heritable connective tissue disease involving multiple organs. Even though the clinical manifestations of MFS can be various, aortic root aneurysm is estimated as one of the most serious complications. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7904104d486d7c09160dea7acdc50ba5
http://link.springer.com/article/10.1186/s13019-020-01304-x
http://link.springer.com/article/10.1186/s13019-020-01304-x
Publikováno v:
BMC Surgery, Vol 21, Iss 1, Pp 1-3 (2021)
BMC Surgery
BMC Surgery
Background Giant superior vena cava (SVC) aneurysm in non-obstructed supracardiac total anomalous pulmonary venous connection (TAPVC) is even more rare than in obstructed one, and this combination has not been reported. Case presentation Here we repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bd9f317f665737119c2e29cb82ab380
https://doaj.org/article/8da2e4d9b2c04cb3806e4527b4f9d0c0
https://doaj.org/article/8da2e4d9b2c04cb3806e4527b4f9d0c0
Publikováno v:
European Heart Journal. 44:430-430
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6b064a686fc1e4e3469359339b31d89
https://doi.org/10.1093/eurheartj/ehac687
https://doi.org/10.1093/eurheartj/ehac687
Publikováno v:
JAMA cardiology. 6(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4961db2d6a0ca4772633eb52cd1b195b
https://pubmed.ncbi.nlm.nih.gov/34369963
https://pubmed.ncbi.nlm.nih.gov/34369963
Giant superior vena cava (SVC) aneurysm in obstructive supracardiac total anomalous venous connection (TAPVC) is rare, and there has not been a giant SVC aneurysm reported in non-obstructive TAPVC. Here we reported a 29‐year‐old female with non-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f31905019ed79cac93faf6717f0a9521
https://doi.org/10.22541/au.160648579.92889179/v1
https://doi.org/10.22541/au.160648579.92889179/v1
