Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Luís Rocha Lopes"'
Autor:
Sílvia Aguiar Rosa, Miguel Mota Carmo, Luís Rocha Lopes, Eunice Oliveira, Boban Thomas, Luis Baquero, Rui Cruz Ferreira, António Fiarresga
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 41, Iss 9, Pp 761-767 (2022)
Introduction and objectives: Coronary microvascular dysfunction (CMD) is one of the most important pathophysiological features in hypertrophic cardiomyopathy (HCM). The index of microcirculatory resistance (IMR) is an invasive method to assess the co
Externí odkaz:
https://doaj.org/article/e72d4b17eed54305ad263c09d058aeaf
Autor:
Pedro Garcia Brás, Sílvia Aguiar Rosa, Boban Thomas, António Fiarresga, Isabel Cardoso, Ricardo Pereira, Gonçalo Branco, Inês Cruz, Luís Baquero, Rui Cruz Ferreira, Miguel Mota Carmo, Luís Rocha Lopes
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 41, Iss 7, Pp 559-568 (2022)
Background: Microvascular dysfunction is an often overlooked feature of hypertrophic cardiomyopathy (HCM). Our aim was to assess the association between microvascular dysfunction, wall thickness, tissue characteristics and myocardial deformation in H
Externí odkaz:
https://doaj.org/article/1d15ff6126cd473d9634c22b8b8299af
Autor:
Pedro Garcia Brás, Sílvia Aguiar Rosa, Isabel Cardoso, Luísa Moura Branco, Ana Galrinho, António Valentim Gonçalves, Boban Thomas, José Miguel Viegas, António Fiarresga, Gonçalo Branco, Ricardo Pereira, Mafalda Selas, Filipa Silva, Inês Cruz, Luís Baquero, Rui Cruz Ferreira, Luís Rocha Lopes
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 8 (2023)
Background Two‐dimensional speckle tracking echocardiography has been shown to correlate with microvascular dysfunction, a hallmark of hypertrophic cardiomyopathy (HCM). We hypothesized that there is an association between myocardial work and left
Externí odkaz:
https://doaj.org/article/69fa93a856be4bb6bdbc29c97ebcc86c
Autor:
Luís Rocha Lopes
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 119, Iss 6, Pp 910-911 (2022)
Externí odkaz:
https://doaj.org/article/08eeff24f5cb44aeb9ac06fa51f113b1
Autor:
Sílvia Aguiar Rosa, Boban Thomas, António Fiarresga, Ana Luísa Papoila, Marta Alves, Ricardo Pereira, Gonçalo Branco, Inês Cruz, Pedro Rio, Luis Baquero, Rui Cruz Ferreira, Miguel Mota Carmo, Luís Rocha Lopes
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Aims: The aim of the study is to investigate the association between the degree of ischemia due to coronary microvascular dysfunction (CMD) and the left ventricular (LV) tissue characteristics, systolic performance, and clinical manifestations in hyp
Externí odkaz:
https://doaj.org/article/baa566ead81147538af97a748ce8db72
Autor:
Nuno Marques, Olga Azevedo, Ana Rita Almeida, Dina Bento, Inês Cruz, Emanuel Correia, Carolina Lourenço, Luís Rocha Lopes
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 19 (2020)
Background The emergence of specific therapies for transthyretin cardiac amyloidosis (CA) warrants the need for a systematic review of the literature. Methods and Results A systematic review of the literature was conducted according to Preferred Repo
Externí odkaz:
https://doaj.org/article/2e1b26f9f7af4b399576d5fdc0334eb3
Autor:
Ana Catarina Gomes, Pedro Santos Barbosa, Ana Coutinho, Inês Cruz, Maria Carmo-Fonseca, Luís Rocha Lopes
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 39, Iss 4, Pp 227.e1-227.e9 (2020)
The authors report the clinical and genetic investigation of a family with hypertrophic cardiomyopathy (HCM). The individuals described are three affected first-degree relatives (father, daughter and son), one affected niece and unaffected nephew and
Externí odkaz:
https://doaj.org/article/4ffc1a7e83df4f01b4347a0ee2f61e9e
Autor:
Dulce Brito, Nuno Cardim, Luís Rocha Lopes, Adriana Belo, Jorge Mimoso, Lino Gonçalves, Hugo Madeira
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 37, Iss 6, Pp 457-466 (2018)
Introduction: In adults, unexplained left ventricular hypertrophy is usually due to sarcomeric hypertrophic cardiomyopathy (HCM). Fabry disease (FD) is rare but may mimic sarcomeric HCM, and has an adverse prognosis in the absence of specific treatme
Externí odkaz:
https://doaj.org/article/4d051fb6ff3b47d5a58bd8de8efb5cb9
Autor:
Nuno Cardim, Dulce Brito, Luís Rocha Lopes, António Freitas, Carla Araújo, Adriana Belo, Lino Gonçalves, Jorge Mimoso, Iacopo Olivotto, Perry Elliott, Hugo Madeira
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 37, Iss 1, Pp 1-10 (2018)
Introduction: We report the results of the Portuguese Registry of Hypertrophic Cardiomyopathy, an initiative that reflects the current spectrum of cardiology centers throughout the territory of Portugal. Methods: A direct invitation to participate wa
Externí odkaz:
https://doaj.org/article/546b91ffee484ef4bcd1bcc9daf59862
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 37, Iss 9, Pp 793-795 (2018)
Externí odkaz:
https://doaj.org/article/2355e1c5821347059e17af7c252188c5