Zobrazeno 1 - 10
of 284
pro vyhledávání: '"Maurizio, Zompatori"'
Autor:
Jonathan Keow, Matthew J. Cecchini, Nathashi Jayawardena, Maurizio Zompatori, Mariamma G. Joseph, Marco Mura
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is associated with increased expression of cyclin-dependent kinase inhibitors such as p16 and p21, and subsequent induction of cell cycle arrest, cellular senescence, and pro-fibrotic gene expre
Externí odkaz:
https://doaj.org/article/6c05baa7dcc4466abc2421858d117edf
Autor:
Paola Faverio, Fabrizio Luppi, Paola Rebora, Gabriele D’Andrea, Anna Stainer, Sara Busnelli, Martina Catalano, Giuseppe Modafferi, Giovanni Franco, Anna Monzani, Stefania Galimberti, Paolo Scarpazza, Elisa Oggionni, Monia Betti, Tiberio Oggionni, Federica De Giacomi, Francesco Bini, Bruno Dino Bodini, Mara Parati, Luca Bilucaglia, Paolo Ceruti, Denise Modina, Sergio Harari, Antonella Caminati, Marcello Intotero, Pietro Sergio, Giuseppe Monzillo, Giovanni Leati, Andrea Borghesi, Maurizio Zompatori, Rocco Corso, Maria Grazia Valsecchi, Giacomo Bellani, Giuseppe Foti, Alberto Pesci
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-12 (2022)
Abstract Background Long-term pulmonary sequelae following hospitalization for SARS-CoV-2 pneumonia is largely unclear. The aim of this study was to identify and characterise pulmonary sequelae caused by SARS-CoV-2 pneumonia at 12-month from discharg
Externí odkaz:
https://doaj.org/article/93ac5ba6289b465b93e182351cff7bad
Autor:
Gian Marco Manzetti, Karishma Hosein, Matthew J. Cecchini, Keith Kwan, Mohamed Abdelrazek, Maurizio Zompatori, Paola Rogliani, Marco Mura
Publikováno v:
BMC Pulmonary Medicine, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is characterized by a poor prognosis, with a progressive decline in lung function and considerable variability in the disease’s natural history. Besides lung transplantation (LTx), the only av
Externí odkaz:
https://doaj.org/article/d941364ce766476cb72b8b4b0e4d70b8
Autor:
Stefano Grecuccio, Nicola Sverzellati, Elisabetta Uslenghi, Antonella Caminati, Giueseppe Pedrazzi, Maurizio Zompatori
Publikováno v:
Diagnostic and Interventional Radiology, Vol 27, Iss 3, Pp 329-335 (2021)
PURPOSEMediastinal lymph node (MLN) enlargement detected on chest computed tomography (CT) is frequent in patients with interstitial lung disease (ILD) and is shown in approximately 70% of cases of idiopathic pulmonary fibrosis (IPF). We hypothesized
Externí odkaz:
https://doaj.org/article/4415f476c6554c2f990d2b306d14d09f
Autor:
Nada Taha, Dejanira D’Amato, Karishma Hosein, Tiziana Ranalli, Gianluigi Sergiacomi, Maurizio Zompatori, Marco Mura
Publikováno v:
Respiratory Research, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background Progression of the disease in idiopathic pulmonary fibrosis (IPF) is difficult to predict, due to its variable and heterogenous course. The relationship between radiographic progression and functional decline in IPF is unclear. We
Externí odkaz:
https://doaj.org/article/fc848c700bc4485289d85e9e30ca7ab6
Autor:
Andrea Sonaglioni, Antonella Caminati, Margherita Re, Davide Elia, Roberta Trevisan, Alberto Granato, Maurizio Zompatori, Michele Lombardo, Sergio Harari
Publikováno v:
Internal and Emergency Medicine. 18:755-767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0c4db05e163fbfcb8f1118d4b2b24f5
https://doi.org/10.1007/s11739-023-03219-6
https://doi.org/10.1007/s11739-023-03219-6
Autor:
Alexander Poellinger, Sabina Berezowska, Jeffrey Leon Myers, Adrian Huber, Manuela Funke-Chambour, Sabina Guler, Thomas Geiser, Sergio Harari, Antonella Caminati, Maurizio Zompatori, Nicola Sverzellati
Publikováno v:
Diagnostics, Vol 12, Iss 4, p 937 (2022)
Background: Fibrosis in pulmonary Langerhans cell histiocytosis (PLCH) histologically comprises a central scar with septal strands and associated airspace enlargement that produce an octopus-like appearance. The purpose of this study was to identify
Externí odkaz:
https://doaj.org/article/fa1dc775938141c2bbf6091f4aae0f63
Autor:
Alessandro Zanasi, Antonio M. Morselli-Labate, Massimiliano Mazzolini, Marianna Mastroroberto, Roberto W. Dal Negro, Ivan Poliacek, Alyn H. Morice, Sara Maio, Giovanni Viegi, Jamie Koufman, Francesco Torresan, Alexandros Ioannou, Daniele Mandolesi, Elisa Liverani, Amedeo Montale, Franco Bazzoli, Fabio Baldi, Maurizio Zompatori, Giovanni A. Fontana, Ahmad Kantar, Peter Dicpinigaitis, Clive Page, Surinder S. Birring, Francesco Tursi
Publikováno v:
Multidisciplinary Respiratory Medicine, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract This paper summarizes the presentations submitted for publication of the 12th AIST National Congress (Associazione Italiana Studio Tosse/Italian Association for Cough Study) entitled “The thousand facets of cough. A clinical and therapeuti
Externí odkaz:
https://doaj.org/article/d92f461bc92e4231b93b2876052984bd
Autor:
Gioacchino Schifino, Maria L Vega, Lara Pisani, Irene Prediletto, Vito Catalanotti, Vittoria Comellini, Ilaria Bassi, Maurizio Zompatori, Marco Vito Ranieri, Stefano Nava
Publikováno v:
European Journal of Internal Medicine. 100:110-118
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c10f95e3269ba9b9ac59db77a6f5c74
https://doi.org/10.1016/j.ejim.2022.04.012
https://doi.org/10.1016/j.ejim.2022.04.012
Autor:
Antonella Caminati, Chiara Lonati, Roberto Cassandro, Davide Elia, Giuseppe Pelosi, Olga Torre, Maurizio Zompatori, Elisabetta Uslenghi, Sergio Harari
Publikováno v:
European Respiratory Review, Vol 28, Iss 153 (2019)
Idiopathic pulmonary fibrosis (IPF) is a progressive and fibrosing lung disease with a poor prognosis. Between 60% and 70% of IPF patients die of IPF; the remaining causes of death may be due to comorbidities occurring in this ageing population. Inte
Externí odkaz:
https://doaj.org/article/07427aa7a02446e08d340642c8ab11e2