Zobrazeno 1 - 10
of 93
pro vyhledávání: '"C. Souto Moura"'
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:
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
Publikováno v:
Revista Portuguesa de Pneumologia (English Edition), Vol 22, Iss 5, Pp 288-290 (2016)
Externí odkaz:
https://doaj.org/article/c0f6fbb5f55e4bd699adcd8d0c791a05
Publikováno v:
Revista Portuguesa de Pneumologia, Vol 18, Iss 3, Pp 109-114 (2012)
Resumo: Introdução: A PET/TC integrada tornou-se num instrumento fundamental na avaliação pré-operatória do cancro do pulmão de não pequenas células (CPNPC), fornecendo informação anatómica e metabólica com util
Externí odkaz:
https://doaj.org/article/8cf56786ba11459e87cea52478b6b5a7
Publikováno v:
Revista Portuguesa de Pneumologia, Vol 17, Iss 4, Pp 186-189 (2011)
Resumo: Existem dados na literatura sobre o uso das propriedades imunomoduladoras de alguns macrólidos no tratamento da pneumonia organizativa criptogénica (COP) como alternativa aos corticoesteróides na doença ligeira ou como adjuvantes da terap
Externí odkaz:
https://doaj.org/article/f2a3a93313eb4a92a9c73e589c399a67
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aafa92db89b135bd23ad04296353cc38
https://doi.org/10.1183/13993003.congress-2022.4094
https://doi.org/10.1183/13993003.congress-2022.4094
Autor:
Rui Cunha, Eva Padrão, Helder Novais Bastos, P. Caetano Mota, C. Souto Moura, S.R. Sousa, José M. C. Pereira, A. Morais, N. Melo, Susana Guimarães
Publikováno v:
Respiratory Medicine Case Reports, Vol 26, Iss, Pp 118-122 (2019)
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::e74ad413b8b014aba18d09c1c8982588
https://doi.org/10.1016/j.rmcr.2018.12.005
https://doi.org/10.1016/j.rmcr.2018.12.005
Publikováno v:
Pulmonology, Vol 27, Iss 5, Pp 464-466 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::671d415109fcf9d31d1dacea06c89571
https://pubmed.ncbi.nlm.nih.gov/33551268
https://pubmed.ncbi.nlm.nih.gov/33551268