Zobrazeno 1 - 10
of 55
pro vyhledávání: '"M. Júlia Maciel"'
Autor:
Gonçalo Pestana, Marta Tavares-Silva, Carla Sousa, Roberto Pinto, Vânia Ribeiro, Mariana Vasconcelos, Pedro Bernardo Almeida, M. Júlia Maciel, Filipe Macedo
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 38, Iss 4, Pp 261-266 (2019)
Introduction: Takotsubo syndrome (TTS) is characterized by transient left ventricular (LV) dysfunction, typically mimicking an anterior wall myocardial infarction (MI), without obstructive coronary artery disease. In the few published reports assessi
Externí odkaz:
https://doaj.org/article/fc66dd54119740ef8f9c7b483091bef9
Autor:
Sofia Torres, Sandra Amorim, Mariana Vasconcelos, Carla Sousa, M. Júlia Maciel, Filipe Macedo
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 38, Iss 7, Pp 515-517 (2019)
Externí odkaz:
https://doaj.org/article/d5e637feb0eb4277b5cc636603b80b08
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 39, Iss 11, Pp 674-675 (2020)
Externí odkaz:
https://doaj.org/article/33665ff238924c0ba5bc110a6521aa14
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 35, Iss 3, Pp 169-177 (2016)
Young athletes are considered the healthiest group in society. Although rare, there are still reports of sudden death or cardiac arrest on the playing fields. Clinical evaluation is of paramount importance for the identification of possible pathologi
Externí odkaz:
https://doaj.org/article/b543af45ae344e729d141dd6e1a744d4
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 32, Iss 6, Pp 517-521 (2013)
Spontaneous coronary artery dissection is a rare cause of acute coronary events or sudden cardiac death. The clinical presentation is highly variable and prognosis varies widely, depending mainly on how rapidly it is diagnosed. Prompt treatment is al
Externí odkaz:
https://doaj.org/article/308e7d4436164144af00397b54c5e618
Autor:
Sílvia Marta Oliveira, Alexandra Gonçalves, Cristina Cruz, Jorge Almeida, António J. Madureira, Isabel Amendoeira, M. Júlia Maciel
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 31, Iss 2, Pp 163-166 (2012)
Cardiac metastases are more common than primary tumors. Several types of malignant tumors have been reported to metastasize to the heart, mainly lung cancer, but in the setting of esophageal cancer, myocardial metastasis is comparatively rare. We rep
Externí odkaz:
https://doaj.org/article/e6befbb4158741c591c3d7d60b9ee51d
Autor:
Ana Lebreiro, Elisabete Martins, Cristina Cruz, Jorge Almeida, Sofia Pimenta, Miguel Bernardes, José Carlos Machado, M. Júlia Maciel, Cassiano Abreu-Lima
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 30, Iss 7, Pp 649-654 (2011)
Resumo: Introdução: O diagnóstico da Síndrome de Marfan (SM) depende fundamentalmente de uma avaliação clínica multidisciplinar. O seu diagnóstico molecular, através da identificação de mutações no gene FBN1, pode permitir estabelecer um
Externí odkaz:
https://doaj.org/article/45debb4b6f36487180867a4ec7e0a403
Autor:
Inês Rangel, Gustavo Barbosa, Carla de Sousa, Pedro Bernardo Almeida, Manuel Campelo, Teresa Pinho, M. Júlia Maciel
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 31, Iss 1, Pp 39-41 (2012)
Resumo: O cálcio assume um papel fundamental na contração e relaxamento do músculo cardíaco. A insuficiência cardíaca hipocalcémica é um distúrbio raro e potencialmente reversível, que traduz esta relação intrínseca.Os autores apresenta
Externí odkaz:
https://doaj.org/article/fbdd6efa0cf64164a4e483bf58d9f95c
Autor:
Carla Sousa, Pedro Almeida, Alexandra Gonçalves, João Rodrigues, Inês Rangel, Filipe Macedo, M. Júlia Maciel
Publikováno v:
Acta Médica Portuguesa, Vol 27, Iss 3 (2014)
Right ventricular thrombosis is a rare yet potentially fatal condition. It has been described in association with hypercoagulability states, autoimmune diseases and dilated cardiomyopathy. Echocardiography constitutes the election tool for diagnosis
Externí odkaz:
https://doaj.org/article/5559c7cbf7d4458894e49572b7dbf0dd
Autor:
Mariana Paiva, Vania Ribeiro, Raquel Garcia, Sandra Amorim, Manuel Campelo, Elisabete Martins, Brenda Moura, Jose Cardoso, M. Júlia Maciel
Publikováno v:
Case Reports in Cardiology, Vol 2012 (2012)
We present a case of a patient with known complete congenital atrioventricular block (CAVB) since the age of 7 years old that developed dilated cardiomyopathy ten years after VVI-R pacemaker implantation. He presented severe biventricular dysfunction
Externí odkaz:
https://doaj.org/article/366347a8e1604938b658092799d84f48