Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Ilaria Campo"'
Autor:
Sara Lettieri, Francesco Bonella, Vincenzo Alfredo Marando, Alessandro N Franciosi, Angelo Guido Corsico, Ilaria Campo
Publikováno v:
European Respiratory Review, Vol 33, Iss 173 (2024)
Pulmonary alveolar proteinosis (PAP) is a syndrome that results from the accumulation of lipoproteinaceous material in the alveolar space. According to the underlying pathogenetic mechanisms, three different forms have been identified, namely primary
Externí odkaz:
https://doaj.org/article/c7a5a23858374066a828728417bf2b73
Autor:
Matteo Della Zoppa, Francesco Rocco Bertuccio, Ilaria Campo, Fady Tousa, Mariachiara Crescenzi, Sara Lettieri, Francesca Mariani, Angelo Guido Corsico, Davide Piloni, Giulia Maria Stella
Publikováno v:
Diagnostics, Vol 14, Iss 7, p 709 (2024)
Sarcoidosis is a multisystem disease, which is diagnosed on a compatible clinical presentation, non-necrotizing granulomatous inflammation in one or more tissue samples, and exclusion of alternative causes of granulomatous disease. Considering its he
Externí odkaz:
https://doaj.org/article/957299e387454a0b9e089265e39413ef
Autor:
Ilaria Campo, Federica Meloni, Martina Gahlemann, Wiebke Sauter, Carina Ittrich, Corinna Schoelch, Bruce C. Trapnell, Abhya Gupta
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disorder involving production of autoantibodies against endogenous granulocyte–macrophage colony-stimulating factor (GM-CSF). This study aimed to identify biomarkers that coul
Externí odkaz:
https://doaj.org/article/6bbf0113c76e4da192f70343cd8f59a7
Autor:
Francesca Mariani, Elena Salvaterra, Sara Lettieri, Annalisa De Silvestri, Alessandra Corino, Matteo Bosio, Elia Fraolini, Davide Piloni, Giuseppe Rodi, Angelo Guido Corsico, Ilaria Campo
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background PAP is an ultra-rare respiratory syndrome characterized by the accumulation of surfactant within the alveoli. Whole lung lavage (WLL) is the current standard of care of PAP, however it is not a standardized procedure and the total
Externí odkaz:
https://doaj.org/article/edc962aaf4bf413a947a7b389d53560a
Autor:
Spyros A. Papiris, Ilaria Campo, Francesca Mariani, Maria Kallieri, Lykourgos Kolilekas, Andriana I. Papaioannou, Efsun Gonca Chousein, Erdogan Cetinkaya, Francesco Bonella, Raphael Borie, Maria Kokosi, Thomas Pickworth, Maria Molina-Molina, Mercè Gasa, Elżbieta Radzikowska, Justyna Fijolek, Stéphane Jouneau, Emmanuel Gomez, Cormac McCarthy, Elisabeth Bendstrup, Wojciech J. Piotrowski, Rishi Pabary, Alice Hadchouel, Nathalie Coolen-Allou, Tiago Alfaro, Carlos Robalo Cordeiro, Elvira-Markela Antonogiannaki, Ioannis P. Tomos, Despoina Papakosta, Theodoros Kontakiotis, Panagiota Panagiotou, Konstantinos Douros, Andrea Schams, Sara Lettieri, Vassiliki Papaevangelou, Christina Kanaka-Gantenbein, Anna Karakatsani, Stelios Loukides, Ulrich Costabel, Bruno Crestani, Cliff Morgan, Ryushi Tazawa, Andrew Bush, Matthias Griese, Effrosyni D. Manali
Publikováno v:
ERJ Open Research, Vol 9, Iss 1 (2023)
Externí odkaz:
https://doaj.org/article/eee5a042a9cc4131bcf3cd18f54c3513
Autor:
Francesco Bonella, Ilaria Campo, Michele Zorzetto, Eda Boerner, Shinichiro Ohshimo, Dirk Theegarten, Christian Taube, Ulrich Costabel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Genetic variants of TOLLIP and MUC5B, both on chromosome 11, have been reported to be associated with the development and/or prognosis of idiopathic pulmonary fibrosis (IPF). This retrospective study was conducted to investigate t
Externí odkaz:
https://doaj.org/article/45be472ec5c94381bbcde77c59d93122
Autor:
Giulia M. Stella, Caterina Marchiò, Elia Bari, Ilaria Ferrarotti, Francesco R. Bertuccio, Antonella Di Gennaro, David Michael Abbott, Paola Putignano, Ilaria Campo, Maria Luisa Torre, Angelo G. Corsico
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 4, p 3496 (2023)
MPM has a uniquely poor somatic mutational landscape, mainly driven by environmental selective pressure. This feature has dramatically limited the development of effective treatment. However, genomic events are known to be associated with MPM progres
Externí odkaz:
https://doaj.org/article/fdfc9c1ced374bf9839852af5c91c5bf
Autor:
Elena Salvaterra, Ilaria Campo
Publikováno v:
Breathe, Vol 16, Iss 2 (2020)
Pulmonary alveolar proteinosis (PAP) is a rare respiratory syndrome characterised by the accumulation of surfactant lipoproteins within the alveoli. According to various pathogenetic mechanisms and aetiologies, PAP is classified as primary, secondary
Externí odkaz:
https://doaj.org/article/08ce075ac63249e7a4ec813309f01741
Autor:
Simona Inghilleri, Patrizia Morbini, Ilaria Campo, Michele Zorzetto, Tiberio Oggionni, Ernesto Pozzi, Maurizio Luisetti
Publikováno v:
Pulmonary Medicine, Vol 2011 (2011)
Background. Idiopathic Pulmonary Fibrosis (IPF) is a fatal lung disease of unknown etiology characterized by interstitial fibrosis determining irreversible distortion of pulmonary architecture. Reactive oxygen species (ROS) and markers of oxidative s
Externí odkaz:
https://doaj.org/article/2a3dfed024394594b3c4dd3b3cf8927e
Autor:
Maurizio Luisetti, Zamir Kadija, Francesca Mariani, Giuseppe Rodi, Ilaria Campo, Bruce C. Trapnell
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 4 (2010)
Pulmonary alveolar proteinosis is a rare condition characterized by the accumulation of lipoproteinaceous material within the airspaces, resulting in impaired gas transfer, and clinical manifestations ranging from asymptomatic to severe respiratory f
Externí odkaz:
https://doaj.org/article/8c12de500fc942f6bc7825fd2efe1b08