Zobrazeno 1 - 10
of 39
pro vyhledávání: '"José Diogo Ferreira Martins"'
Autor:
Sérgio Laranjo, Glória Costa, Isabel Freitas, José Diogo Ferreira Martins, Luís Bakero, Conceição Trigo, Isabel Fragata, José Fragata, Fátima F. Pinto
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 34, Iss 5, Pp 347-355 (2015)
Introduction: Hypoplastic left heart syndrome (HLHS) is a major cause of cardiac death during the first week of life. The hybrid approach is a reliable, reproducible treatment option for patients with HLHS. Herein we report our results using this app
Externí odkaz:
https://doaj.org/article/6298862f0dff437c8ae9ac9948b49116
Autor:
Boban Thomas, José Diogo Ferreira Martins, Nuno Jalles Tavares, Artur Lopes, Fátima F Pinto, José Fragata
Publikováno v:
Annals of Pediatric Cardiology, Vol 6, Iss 1, Pp 29-33 (2013)
Background: The neonatal arterial switch operation (ASO) is now the standard of care for children born with transposition of the great arteries. Stenosis of the neopulmonary artery on long-term follow up is a known complication. Methods: We performe
Externí odkaz:
https://doaj.org/article/e0c2b3b295cc4f85936ae509d7eb316d
Autor:
Sofia Gouveia, José Diogo Ferreira Martins, Glória Costa, Filipa Paramés, Isabel Freitas, Mónica Rebelo, Conceição Trigo, Fátima F. Pinto
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 30, Iss 11, Pp 849-854 (2011)
Resumo: Introdução: A válvula aórtica quadricúspide é uma malformação rara, com uma incidência estimada de 0,003 a 0,043% de todas as cardiopatias congénitas. Surge habitualmente como uma anomalia congénita isolada, podendo igualmente esta
Externí odkaz:
https://doaj.org/article/d3d41623d3e9430088026ac7a0d1cda2
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 31, Iss 5, Pp 403-404 (2012)
Externí odkaz:
https://doaj.org/article/1305d6c497d14aa6a8787277fed1ef9a
Autor:
Carla Favoccia, Neerod Kumar Jha, Magdi Tofeig, Massimo Chessa, Mohammad Daud Khan, Andreas Eicken, Gianfranco Butera, José Diogo Ferreira Martins, Luis Fernandez Gonzalez, Fátima Pinto, Mario Carminati
Publikováno v:
EuroIntervention. 16:e1274-e1280
AIMS Aortic arch atresia (AAA) is one of the rarest obstructive defects. The presence of this anomaly in adult age is uncommon. The typical anatomic feature consists of a complete occlusion of the membranous obstruction resulting in an acquired atres
Publikováno v:
Annals of Pediatric Cardiology, Vol 12, Iss 3, Pp 329-332 (2019)
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology
Coronary artery fistulas (CAFs) are rare abnormal communications between a normal coronary artery and a cardiac chamber or great vessel, such as the pulmonary artery, bypassing the myocardial capillary network. We report the case of a 17-year-old mal
Publikováno v:
Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care ISBN: 9781447149996
Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care
Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d37279f6a1e7da06e656ef48bf4062a
https://doi.org/10.1007/978-1-4471-4999-6_28-2
https://doi.org/10.1007/978-1-4471-4999-6_28-2
Autor:
Fátima F. Pinto, Hugo Marques, José Diogo Ferreira Martins, Susana M. Abreu, Marta de Antonio
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 40, Iss 10, Pp 707-712 (2021)
Introduction: Mortality and morbidity in patients with transposition of the great arteries after an arterial switch operation depends mainly on the status of coronary perfusion. Coronary computed tomography angiography (CCTA) provides accurate inform
Autor:
José Fragata, Lídia M Sousa, Fátima F. Pinto, Rui Cerejo, Rui Rodrigues, Carolina Torres, José Diogo Ferreira Martins
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Hutchinson-Gilford progeria syndrome is a rare genetic disorder, characterized by progressive premature aging and early death in the first or second decade of life, usually secondary to cardiovascular events (myocardial infarction and stroke). We rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bfee2033bfdc30fd00d4bfd0b791caa
https://hdl.handle.net/10400.17/3659
https://hdl.handle.net/10400.17/3659
Autor:
Tal Geva, Elif Seda Selamet Tierney, Marta de Antonio, Sarah D. de Ferranti, Boban Thomas, Shelby Kutty, José Diogo Ferreira Martins, Uyen Truong, Miguel Mota Carmo, Justin P. Zachariah, Ashwin Prakash, Maria P. Guarino, Nuno Jalles, Shaine A. Morris, António Marinho, Diana Oliveira, Kimberlee Gauvreau
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Background Optimally treated patients with coarctation of the aorta remain at risk for late vascular dysfunction. The effect of treatment modality on vascular function is unknown. The LOVE‐COARCT (Long‐term Outcomes and Vascular Evaluation After