Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Manuel Pedro, Magalhães"'
Autor:
Valdano Manuel, Humberto Morais, Manuel Pedro Magalhães, Maria Ana Sampaio Nunes, Gilberto Leon, Manuel Ferreira, António Pedro Filipe Júnior
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 34, Iss 10, Pp 607-612 (2015)
Introduction and Objective: Ebstein's anomaly is a rare complex congenital heart defect of the tricuspid valve. We aimed to describe the frequency, clinical profile, and early and short-term post-operative results in patients under the age of 18 year
Externí odkaz:
https://doaj.org/article/0c65cc493ef74961bf55e891cdcdc82e
Autor:
Paulo G. Pedro, Berta Carôla, Rui Conduto, Isabel Barão, Rui Cruz Ferreira, Manuel Pedro Magalhães
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 32, Iss 5, Pp 443-445 (2013)
Externí odkaz:
https://doaj.org/article/e274e645d3e4456da2adb415c361a1c2
Autor:
Miguel Sousa Uva, Ana Henriques, Patrícia Heitor, Valdano Manuel, António P. F. Júnior, Manuel Pedro Magalhães, M A Nunes, Gade Miguel
Publikováno v:
Cardiology in the Young. 27:1755-1763
BackgroundEpidemiological patterns of cardiac disease differ between developed countries and African nations. Despite the collaborative efforts of developed countries, several obstacles hinder the implementation of successful programmes for the manag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ac923c0ff790e471873eb86ccc5b3d7
https://doi.org/10.1017/s1047951117001202
https://doi.org/10.1017/s1047951117001202
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
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Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::53c8ef878424281f5ec3923987d0e710
Autor:
Filipa Paramés, José Fragata, Fátima F. Pinto, Isabel Freitas, Mónica Rebelo, Conceição Trigo, Luís Bakero, José Diogo Ferreira Martins, Manuel Pedro Magalhães
Publikováno v:
Cardiology in the Young. 24:447-452
Objectives: This publication aims to report the cases of four children with pseudoaneurysm of the mitral-aortic intervalvular fibrosa and carry out a review of the literature. Background: Pseudoaneurysm of the mitral-aortic intervalvular fibrosa is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9e466a0988b094e3af345346515ed5
https://doi.org/10.1017/s1047951113000590
https://doi.org/10.1017/s1047951113000590
Autor:
Fátima Pinto, Conceição Trigo, Isabel Fragata, José Fragata, Manuel Pedro Magalhães, Luís Baquero
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 4:44-49
Partial anomalous pulmonary venous connections (PAPVCs) are a heterogeneous group of congenital heart lesions in which at least one pulmonary vein will drain into the systemic venous system. The consequences are a variable left-to-right hemodynamic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9df1c49e694657b02780a9238106d3d
https://doi.org/10.1177/2150135112460250
https://doi.org/10.1177/2150135112460250
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery. :13-17
Amac: Atriyoventrikuler septal defektler (AVSD’ler) degisik formlarda klinik bulgulari olan oldukca degisken dogustan malformasyonlari icerir. Calisma plani: Bu calismada, bu dogustan kardiyak malformasyon tipine iliskin olarak, tek bir m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90a73db46ef80280df7b8cc867ec1bf4
https://doi.org/10.5606/tgkdc.dergisi.2011.03suppl1
https://doi.org/10.5606/tgkdc.dergisi.2011.03suppl1
Autor:
Valdano Manuel, Humberto Morais, Manuel Pedro Magalhães, Antonio Pedro Filipe Junior, M A Nunes, Gade Miguel
Publikováno v:
World journal for pediatriccongenital heart surgery. 7(4)
We report an incidental finding of pseudoaneurysm in a 10-month-old boy with tetralogy of Fallot and Down syndrome who had undergone placement of a modified Blalock-Taussig shunt at age four months. Computed tomography was a determinant exam for bett
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23d45d7ccbbc4762c793f36901b5499b
https://pubmed.ncbi.nlm.nih.gov/27358305
https://pubmed.ncbi.nlm.nih.gov/27358305
Autor:
Valdano Manuel, António P. F. Júnior, Humberto Morais, Sebastiana Gamboa, M A Nunes, Manuel Pedro Magalhães, Albino Pedro, Gade Miguel, Miguel Sousa-Uva
Publikováno v:
World journal for pediatriccongenital heart surgery. 6(4)
Background: Anomalous origin of one pulmonary artery is a rare congenital heart disease in which one pulmonary artery branch originates from the ascending aorta. Objective: To describe the experience of a cardiothoracic center in an African country t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ecb1211c2093ca01fca2e1e469d8df9
https://pubmed.ncbi.nlm.nih.gov/26467865
https://pubmed.ncbi.nlm.nih.gov/26467865
Publikováno v:
Journal of Cardiovascular Diseases & Diagnosis.
Cardiothoracic ratio upper to 0.60 is a fact of poor prognostic in patients with Ebstein’s anomaly and the prognostic is worse if is associated with others congenital heart disease. We present 4-months black boy with Ebstein’s anomaly associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17ddf23993df02cd59092a71f0b1ee63
https://doi.org/10.4172/2329-9517.1000188
https://doi.org/10.4172/2329-9517.1000188