Zobrazeno 1 - 10
of 193
pro vyhledávání: '"Giovanni Taccetti"'
Autor:
Vito Terlizzi, Tommaso Ballerini, Alice Castaldo, Daniela Dolce, Silvia Campana, Giovanni Taccetti, Elena Chiappini
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Recurrent respiratory infections are a leading cause of morbidity and mortality in persons with Cystic Fibrosis (pwCF). Recently, the emergence of Nocardia species as a potential pathogen in CF has raised questions about its role
Externí odkaz:
https://doaj.org/article/84d2690ca2224839bcf4393e3d589c77
Autor:
Karina Kleinfelder, Paola Melotti, Anca Manuela Hristodor, Cristina Fevola, Giovanni Taccetti, Vito Terlizzi, Claudio Sorio
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Predictions based on patient-derived materials of CFTR modulators efficacy have been performed lately in patient-derived cells, extending FDA-approved drugs for CF patients harboring rare variants. Here we developed intestinal org
Externí odkaz:
https://doaj.org/article/e49aa8d519cc46a4aa28df4276322072
Autor:
Barry J Plant, Daniel Peckham, Pierre-Régis Burgel, Alan Smyth, Andreas Jung, Manfred Ballmann, Giovanni Taccetti, Harry Heijerman, Pavel Drevinek, Jochen G Mainz, Carsten Schwarz
Publikováno v:
BMJ Open Respiratory Research, Vol 11, Iss 1 (2024)
The major cause of mortality in people with cystic fibrosis (pwCF) is progressive lung disease characterised by acute and chronic infections, the accumulation of mucus, airway inflammation, structural damage and pulmonary exacerbations. The prevalenc
Externí odkaz:
https://doaj.org/article/ce777e645bdb4ad08771fda0a6783f30
Autor:
Daniela Dolce, Novella Ravenni, Cristina Fevola, Michela Francalanci, Paolo Bonomi, Maria Chiara Cavicchi, Valeria Galici, Anna Silvia Neri, Giovanni Taccetti, Vito Terlizzi, Diletta Innocenti, Beatrice Ferrari, Chiara Bianchimani, Erica Camera, Tommaso Orioli, Silvia Campana
Publikováno v:
Heliyon, Vol 10, Iss 5, Pp e26978- (2024)
Background: The upper airways of cystic fibrosis (CF) persons are an evolutionary niche where genetically adapted bacterial strains are selected for lung infection. The microbiological studies conducted up to now on the upper airways are not easily c
Externí odkaz:
https://doaj.org/article/a95d21a0cdc24eabb44dcdf92becc667
Autor:
Alice Castaldo, Monica Gelzo, Paola Iacotucci, Annalisa Longobardi, Giovanni Taccetti, Vito Terlizzi, Vincenzo Carnovale
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2024)
Introduction: Modulators of cystic fibrosis transmembrane conductance regulator mutated protein significantly improved the outcome of patients with cystic fibrosis (CF). We describe 63 patients who were independently followed up in two CF regional ce
Externí odkaz:
https://doaj.org/article/d96ddba11e9b4871b12efa9b630f883e
Autor:
Vito Terlizzi, Marco Antonio Motisi, Roberta Pellegrino, Luisa Galli, Giovanni Taccetti, Elena Chiappini
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-17 (2023)
Abstract Invasive pulmonary aspergillosis (IPA) is a severe condition in immunocompromised children, but the optimal management is still under debate. In order to better clarify this issue, a literature search was performed through MEDLINE/PubMed dat
Externí odkaz:
https://doaj.org/article/23e914c4e79c437fab2379b6298df4cb
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-7 (2022)
Abstract Cystic fibrosis (CF) is the most common inherited disease in Caucasian populations, affecting around 50,000 patients in Europe and 30,000 in United States. A mutation in CF trans-membrane conductance regulator (CFTR) gene changes a protein (
Externí odkaz:
https://doaj.org/article/00997ef1ca204c7d9f57b2afdbbfb777
Autor:
Diletta Innocenti, Chiara Castellani, Eleonora Masi, Valeria Galici, Letizia Macconi, Giovanni Taccetti
Publikováno v:
Monaldi Archives for Chest Disease (2023)
Lung disease in cystic fibrosis (CF) is characterized by reduced mucociliary clearance, airway plugging, recurrent infections and chronic pulmonary inflammation. Patients who are affected undergo daily respiratory physiotherapy to improve airway clea
Externí odkaz:
https://doaj.org/article/4a13155feb8f4037aaf9b9a04e469aa3
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 9, Pp n/a-n/a (2022)
Externí odkaz:
https://doaj.org/article/256a9b1bdd6140c2afc509b51d63e644
Autor:
Daniela Dolce, Cristina Fevola, Erica Camera, Tommaso Orioli, Ersilia Lucenteforte, Marco Andrea Malanima, Giovanni Taccetti, Vito Terlizzi
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 3, p 41 (2023)
The sweat test (ST) is the current diagnostic gold standard for cystic fibrosis (CF). Many CF centres have switched from the Gibson–Cooke method to the Macroduct system-based method. We used these methods simultaneously to compare CF screening outc
Externí odkaz:
https://doaj.org/article/36877e53dbbc43208e0f340c1619e059