Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Nair Yukie Maeda"'
Autor:
Eloisa Sassá Carvalho, Juliano Gomes Penha, Nair Yukie Maeda, Kelly Cristina O. Abud, Maria Francilene S. Souza, Claudia R. P. Castro, Johnny X. dos Santos, Juliana Pereira, Antonio Augusto Lopes
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Although Down syndrome (DS) is considered a risk factor for hemodynamic instabilities (mainly pulmonary hypertension–PH) following surgery for congenital cardiac communications, many DS patients do surprising well postoperatively. We prosp
Externí odkaz:
https://doaj.org/article/b3a711092e644569851e925b21e09dbf
Autor:
Leína Zorzanelli, Nair Yukie Maeda, Mariana Meira Clavé, Vera Demarchi Aiello, Marlene Rabinovitch, Antonio Augusto Lopes
Publikováno v:
Mediators of Inflammation, Vol 2016 (2016)
Background and Objective. Inflammation is central in the pathogenesis of pulmonary hypertension. We investigated how serum cytokines correlate with clinical features, hemodynamics, and lung histology in young patients with pulmonary hypertension asso
Externí odkaz:
https://doaj.org/article/0dbdb29151194fffaca232ae79628c4e
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 70, Iss 3, Pp 141-145 (1998)
OBJETIVO: Avaliar alterações quantitativas e estruturais do fator von Willebrand (fvW) circulante em 40 pacientes com hipertensão pulmonar pré-capilar e verificar possíveis implicações prognósticas dos resultados iniciais, em um ano de seguim
Externí odkaz:
https://doaj.org/article/763a9b72ebe74ae3807c779ef6563e88
Autor:
Luiz J. Kajita, Nair Yukie Maeda, Sérgio Paulo Bydlowski, Vera Demarchi Aiello, Antonio Augusto Lopes, Paulo Caleb Junior Lima Santos, Ana Maria Thomaz
Publikováno v:
Mediators of Inflammation, Vol 2019 (2019)
Mediators of Inflammation
Mediators of Inflammation
Macrophage migration inhibitory factor (MIF) plays an important pathophysiological role in pulmonary hypertension (PHT). Previously, we demonstrated that serum MIF is increased in pediatric PHT associated with congenital heart disease (CHD). In the p
Autor:
Nair Yukie Maeda, Mariana M Clavé, Sérgio Paulo Bydlowski, Claudia Regina Pinheiro Castro, Antonio Augusto Lopes
Publikováno v:
Pulmonary Circulation
In patients with Eisenmenger syndrome, life expectancy is usually longer than in patients with other forms of pulmonary arterial hypertension (PAH). We conducted a cohort study in which patients were followed over a long period of time in an attempt
Autor:
Claudia R. Castro, Maria Francilene Silva Souza, Nair Yukie Maeda, Leína Zorzanelli, Eloisa S. Carvalho, Antonio Augusto Lopes, Ana Maria Thomaz, Juliana Pereira
Publikováno v:
Cytokine. 134:155192
Inflammation and immunity are central in the pathobiology of pulmonary vascular disorders. Preliminary headway has been made in understanding the relationships between inflammatory proteins and clinical parameters in pediatric congenital heart diseas
Autor:
Antonio Augusto Lopes, Nair Yukie Maeda, Sérgio Paulo Bydlowski, Ana Maria Thomaz, Mariana M Clavé
Publikováno v:
Congenital heart disease. 14(2)
BACKGROUND Ideally, vasodilator therapies for pulmonary arterial hypertension (PAH) should have a favorable impact on markers of vascular dysfunction, in addition to their known effects on hemodynamics, cardiac function, and patient's physical capaci
Autor:
Nair Yukie Maeda, Giuseppe Palmisano, Livia Rosa-Fernandes, Luciana M. F. Maselli, Sérgio Paulo Bydlowski
Publikováno v:
Chemistry and physics of lipids. 207
Oxysterols are cholesterol oxidation products formed through enzymatic or autoxidation mechanisms. 7-ketocholeterol (7KC) is one of most abundant oxysterols found in atherosclerotic lesions. Its role in atherosclerosis pathogenesis has been broadly s
Autor:
Ana Maria Thomaz, Mariana M Clavé, Filomena Regina Barbosa Gomes Galas, Nair Yukie Maeda, Leína Zorzanelli, Marlene Rabinovitch, Antonio Augusto Lopes
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
In congenital heart disease, severity of pulmonary hypertension and operability is defined by noninvasive parameters (clinical history, physical examination, and echocardiography) and sometimes, cardiac catheterization. We investigated how circulatin
Autor:
Nair Yukie Maeda, Antonio Augusto Lopes, Mariana M Clavé, Sonia M Mesquita, Sérgio Paulo Bydlowski
Publikováno v:
Circulation. 132
Background: Patients with pulmonary arterial hypertension (PAH) associated with the Eisenmeger syndrome (ES) frequently have decreased platelet counts and aggregation. This is probably due to chronic endogenous platelet activation and consumption ass