Zobrazeno 1 - 10
of 93
pro vyhledávání: '"C Souto Moura"'
Publikováno v:
Pulmonology, Vol 29, Iss 1, Pp 89-91 (2023)
Externí odkaz:
https://doaj.org/article/e030dd25e0984e5aab5b5fcaa99bcf56
Publikováno v:
Pulmonology, Vol 27, Iss 5, Pp 464-466 (2021)
Externí odkaz:
https://doaj.org/article/8b6f8c91429445009429c7763e4d4f42
Autor:
V. Santos, N. Martins, C. Sousa, M. Jacob, E. Padrão, N. Melo, P. Caetano Mota, H.N. Bastos, S. Guimarães, C. Souto Moura, O. Sokhatska, R. Cunha, J. Pereira, A. Morais
Publikováno v:
Pulmonology, Vol 26, Iss 3, Pp 130-137 (2020)
Hypersensitivity pneumonitis (HP) is an interstitial lung disease (ILD) which varies in prevalence across the world, depending on disease definition, diagnostic methods, exposure type and intensity, geographical environments, agricultural and industr
Externí odkaz:
https://doaj.org/article/5950ba9addd74eceb74435a6a9c1af5a
Autor:
S.R. Sousa, P. Caetano Mota, N. Melo, H.N. Bastos, E. Padrão, J.M. Pereira, R. Cunha, C. Souto Moura, S. Guimarães, A. Morais
Publikováno v:
Respiratory Medicine Case Reports, Vol 26, Iss , Pp 118-122 (2019)
Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease of unknown cause that occurs sporadically, but it can also occur in families and so named as Familial Pulmonary Fibrosis (FPF). Some forms of FPF overlaps IPF features, namely
Externí odkaz:
https://doaj.org/article/76c9962e3aaa42229d430af731499364
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
Autor:
S C Dias, N Faria, M Silva, D Carvalho, A Carvalho, P Caetano Mota, N Melo, H Novais-Bastos, A Terras Alexandre, C Souto Moura, S Guimarães, O Sokhatska, R Cunha, J M Pereira, A Morais
Publikováno v:
12.01 - Idiopathic interstitial pneumonias.
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 22, Iss 5, Pp 288-290 (2016)
Externí odkaz:
https://doaj.org/article/c0f6fbb5f55e4bd699adcd8d0c791a05
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