Cargando…
Ultra-rare cystic disease
Diffuse cystic lung diseases include a group of heterogeneous disorders characterised by the presence of cysts within the lung parenchyma, sometimes showing a characteristic computed tomography scan pattern that allows diagnosis. The pathogenetic mechanisms underlying cyst formation in the lung are...
Autores principales: | Elia, Davide, Torre, Olga, Cassandro, Roberto, Caminati, Antonella, Harari, Sergio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489057/ https://www.ncbi.nlm.nih.gov/pubmed/32878971 http://dx.doi.org/10.1183/16000617.0163-2019 |
Ejemplares similares
-
Severe idiopathic pulmonary fibrosis: what can be done?
por: Caminati, Antonella, et al.
Publicado: (2017) -
Comorbidities in idiopathic pulmonary fibrosis: an underestimated issue
por: Caminati, Antonella, et al.
Publicado: (2019) -
New insights in lymphangioleiomyomatosis and pulmonary Langerhans cell histiocytosis
por: Torre, Olga, et al.
Publicado: (2017) -
Pulmonary hypertension and chronic lung disease: where are we headed?
por: Elia, Davide, et al.
Publicado: (2019) -
Charlson comorbidity index, neutrophil-to-lymphocyte ratio and undertreatment with renin-angiotensin-aldosterone system inhibitors predict in-hospital mortality of hospitalized COVID-19 patients during the omicron dominant period
por: Sonaglioni, Andrea, et al.
Publicado: (2022)