Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Guadalupe Bermudo Peloche"'
Publikováno v:
Medical Sciences, Vol 6, Iss 3, p 71 (2018)
Though idiopathic pulmonary fibrosis (IPF) is characterized by single-organ involvement, many comorbid conditions occur within other organ systems. Patients with IPF may present during evolution different complications and comorbidities that influenc
Externí odkaz:
https://doaj.org/article/b19b178215e84262a15b216b7c25673a
Publikováno v:
Revista de Patología Respiratoria, Vol 26, Iss 2 (2023)
La neumonía organizativa es un patrón histológico que puede observarse asociado o reactivo en diferentes patologías. Presentamos el caso de una mujer de 67 años con diagnóstico inicial de neumonía organizada criptogénica, sin respuesta a los
Externí odkaz:
https://doaj.org/article/29b3fb00f84f4aaebe4a044942c04643
Autor:
Jaume Bordas-Martínez, Ricard Gavaldà, Jessica G. Shull, Vanesa Vicens-Zygmunt, Lurdes Planas-Cerezales, Guadalupe Bermudo-Peloche, Salud Santos, Neus Salord, Carmen Monasterio, Maria Molina-Molina, Guillermo Suarez-Cuartin
Publikováno v:
ERJ Open Research, Vol 7, Iss 2 (2021)
Introduction Idiopathic pulmonary fibrosis (IPF) prognosis is heterogeneous despite antifibrotic treatment. Cluster analysis has proven to be a useful tool in identifying interstitial lung disease phenotypes, which has yet to be performed in IPF. The
Externí odkaz:
https://doaj.org/article/71adfdbbda074442b4929502caabd9c3
Autor:
Carmen Monasterio, √anesa Vicens-Zygmunt, Salud Santos, Jaume Bordas-Martinez, Maria Molina-Molina, Guadalupe Bermudo-Peloche, Ricard Gavaldà, Jessica Shull, Guillermo Suarez-Cuartin, Lurdes Planas-Cerezales, Neus Salord
Publikováno v:
Idiopathic interstitial pneumonias.
Introduction: Idiopathic pulmonary fibrosis (IPF) prognosis is heterogeneous despite antifibrotic treatment. Cluster analysis has proven to be a useful tool in identifying interstitial lung disease phenotypes, which has yet to be performed in IPF. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddee50a99338fc224014e70c4b7c89ad
https://doi.org/10.1183/13993003.congress-2021.pa3745
https://doi.org/10.1183/13993003.congress-2021.pa3745
Autor:
Carmen Monasterio, Guillermo Suarez-Cuartin, Lurdes Planas-Cerezales, Neus Salord, Salud Santos, Ricard Gavaldà, Maria Molina-Molina, Vanesa Vicens-Zygmunt, Guadalupe Bermudo-Peloche, Jessica Shull, Jaume Bordas-Martinez
Publikováno v:
ERJ Open Research
article-version (VoR) Version of Record
ERJ Open Research, Vol 7, Iss 2 (2021)
article-version (VoR) Version of Record
ERJ Open Research, Vol 7, Iss 2 (2021)
Introduction Idiopathic pulmonary fibrosis (IPF) prognosis is heterogeneous despite antifibrotic treatment. Cluster analysis has proven to be a useful tool in identifying interstitial lung disease phenotypes, which has yet to be performed in IPF. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e031aa826371a618fcd9b60a645ac9b8
http://europepmc.org/articles/PMC8107351
http://europepmc.org/articles/PMC8107351
Autor:
José Antonio Rodríguez-Portal, Guillermo Suarez-Cuartin, Jaume Sauleda, Ana Romero, Maria Molina-Molina, Orlando Acosta Fernández, Esteban Cano-Jiménez, Pilar Rivera Ortega, Karina Portillo, Diego Castillo, Eva Balcells, Guadalupe Bermudo Peloche, Claudia Valenzuela, Myriam Aburto, Belén Núñez, Virginia Leiro, Ana Villar, Vanesa Vicens-Zygmunt, Estrella Fernández-Fabrellas, Amalia Moreno, Rosario Laporta, Maria Teresa González-Budiño, Lurdes Planas-Cerezales
Publikováno v:
European Respiratory Journal
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd8228412290db083638b4227c2209e7
https://doi.org/10.1183/13993003.congress-2020.765
https://doi.org/10.1183/13993003.congress-2020.765
Autor:
Orlando Acosta Fernández, Núria Padullés Zamora, Jose Manuel Palma López, Jordi Dorca Sargatal, Agustín Medina Gonzálvez, Jaume Bordas Martinez, Ramón José Jódar Masanés, Laura Pérez Martín, Guadalupe Bermudo Peloche, Guillermo Suarez-Cuartin, Lurdes Planas-Cerezales, Maria Molina Molina, Vanesa Vicens Zygmunt, Ana Belén Llanos-González, Sara García Gil
Publikováno v:
Idiopathic interstitial pneumonias.
Introduction and Aim: Pirfenidone and nintedanib are anti-fibrotic approved treatments for idiopathic pulmonary fibrosis (IPF). Its efficacy and safety in other fibrotic interstitial lung diseases (ILD) is under study in clinical trials. The aim was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bdd32acc62c9a6c20ff1e55e883a372
https://doi.org/10.1183/13993003.congress-2019.pa1731
https://doi.org/10.1183/13993003.congress-2019.pa1731
Publikováno v:
Medical Sciences, Vol 6, Iss 3, p 71 (2018)
Medical Sciences
Medical Sciences
Though idiopathic pulmonary fibrosis (IPF) is characterized by single-organ involvement, many comorbid conditions occur within other organ systems. Patients with IPF may present during evolution different complications and comorbidities that influenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d969fdf729f7a14c0dd5a22772c8b274
https://doi.org/10.3390/medsci6030071
https://doi.org/10.3390/medsci6030071