Zobrazeno 1 - 10
of 62
pro vyhledávání: '"J.M. Jesus"'
Autor:
C. Robalo-Cordeiro, P. Campos, L. Carvalho, A. Borba, S. Clemente, S. Freitas, S. Furtado, J.M. Jesus, C. Leal, A. Marques, N. Melo, C. Souto-Moura, S. Neves, V. Sousa, A. Santos, A. Morais
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 23, Iss 5, Pp 287-293 (2017)
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal lung disease that up to now has been associated with a poor prognosis. However, the results of the INPULSIS and ASCEND trials and the approval of nintedanib and pirfenidone have marked th
Externí odkaz:
https://doaj.org/article/cfa5b1793e0a44c1b23a2902a16e5b13
Autor:
A.V. Cardoso, P.C. Mota, N. Melo, S. Guimarães, C. Souto Moura, J.M. Jesus, R. Cunha, A. Morais
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 23, Iss 5, Pp 251-258 (2017)
Background: Sarcoidosis is a systemic granulomatous disease of unknown etiology. Epidemiological studies of different populations are essential because clinical presentation, organ involvement, disease severity, and prognosis vary significantly accor
Externí odkaz:
https://doaj.org/article/6a883015d23b460785302837ab808b8a
Autor:
C. Robalo Cordeiro, P. Campos, L. Carvalho, S. Campainha, S. Clemente, L. Figueiredo, J.M. Jesus, A. Marques, C. Souto-Moura, R. Pinto Basto, A. Ribeiro, M. Serrado, A. Morais
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 22, Iss 2, Pp 112-122 (2016)
Idiopathic pulmonary fibrosis is a rare interstitial lung disease included in the Idiopathic Interstitial Pneumonias group. Although several potential risk factors have been described, it is a progressive fibrosing disease of unknown cause affecting
Externí odkaz:
https://doaj.org/article/6ea26670ac8a4c1fb5950f97fa62c853
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 21, Iss 1, Pp 41-44 (2015)
Idiopathic pleuroparenchymal fibroelastosis (IPPFE) is a recently described rare entity, characterized by pleural and subpleural parenchymal fibrosis and elastosis mainly in the upper lobes. The etiology and pathophysiology are unknown. The prognosis
Externí odkaz:
https://doaj.org/article/4af407119be24f9292c71b7390a7c073
Autor:
F. Soares Pires, P. Caetano Mota, N. Melo, D. Costa, J.M. Jesus, R. Cunha, S. Guimarães, C. Souto-Moura, A. Morais
Publikováno v:
Revista Portuguesa de Pneumologia, Vol 19, Iss 1, Pp 19-27 (2013)
Resumo: Introdução: A Fibrose Pulmonar Idiopática (FPI) é a patologia mais comum no subgrupo das pneumonias intersticiais idiopáticas. Apesar de uma grande variabilidade no tipo de evolução clÃnica, está inexoravelmente ass
Externí odkaz:
https://doaj.org/article/ec929a1ef06147d8959d8fa7d35bf851
Autor:
Patrícia Caetano Mota, Conceição Souto-Moura, Susana Guimarães, Mafalda Martins Baptista, André F. Carvalho, Natália Melo, Rui Cunha, Helder Novais Bastos, J.M. Jesus, António Morais
Publikováno v:
Rare ILD / DPLD.
Autor:
Vanessa Santos, Natália Melo, Patrícia Caetano Mota, António Morais, Marta Drummond, Nuno Sousa Pereira, Ana Verónica Cardoso, Inês Neves, J.M. Jesus
Publikováno v:
Canadian Journal of Respiratory Therapy: CJRT = Revue Canadienne de la Thérapie Respiratoire : RCTR
Introduction Recent studies have reported a high prevalence of obstructive sleep apnoea (OSA) among patients with diffuse parenchymal lung disease (DPLD), mainly idiopathic pulmonary fibrosis (IPF). Effective OSA treatment appears to have a positive
Autor:
A. Borba, C. Leal, S. Freitas, S. Clemente, S. Furtado, J.M. Jesus, Ana-Cristina Santos, Conceição Souto-Moura, P. Campos, António Morais, Vitor Sousa, C. Robalo-Cordeiro, Lina Carvalho, S. F. Neves, N. Melo, Agostinho Marques
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Revista Portuguesa de Pneumologia (English Edition), Vol 23, Iss 5, Pp 287-293 (2017)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Revista Portuguesa de Pneumologia (English Edition), Vol 23, Iss 5, Pp 287-293 (2017)
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal lung disease that up to now has been associated with a poor prognosis. However, the results of the INPULSIS and ASCEND trials and the approval of nintedanib and pirfenidone have marked th
Autor:
Rui Cunha, Susana Guimarães, Patrícia Caetano Mota, C. Souto Moura, J.M. Jesus, A. Morais, Ana Verónica Cardoso, N. Melo
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 23, Iss 5, Pp 251-258 (2017)
Background: Sarcoidosis is a systemic granulomatous disease of unknown etiology. Epidemiological studies of different populations are essential because clinical presentation, organ involvement, disease severity, and prognosis vary significantly accor
The Fourier coefficients v2 and v3 characterizing the anisotropy of the azimuthal distribution of charged particles produced in PbPb collisions at sNN=5.02 TeV are measured with data collected by the CMS experiment. The measurements cover a broad tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::44be75554579e903503d39c29d942729
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3072300
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3072300