Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Valeria Galici"'
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:
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
Autor:
Matteo Botti, Vito Terlizzi, Michela Francalanci, Daniela Dolce, Maria Chiara Cavicchi, Anna Silvia Neri, Valeria Galici, Gianfranco Mergni, Lucia Zavataro, Claudia Centrone, Filippo Festini, Giovanni Taccetti
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Abstract Background Cystic fibrosis (CF) is a life-threatening disease affecting about 1:3000 newborns in Caucasian populations. The introduction of newborn screening for cystic fibrosis (CF NBS) has improved the clinical outcomes of individuals with
Externí odkaz:
https://doaj.org/article/2cd82b90d17544b1ba359d6a11113bc5
Autor:
Pierluigi Ciet, Silvia Bertolo, Mirco Ros, Rosaria Casciaro, Marco Cipolli, Stefano Colagrande, Stefano Costa, Valeria Galici, Andrea Gramegna, Cecilia Lanza, Francesca Lucca, Letizia Macconi, Fabio Majo, Antonella Paciaroni, Giuseppe Fabio Parisi, Francesca Rizzo, Ignazio Salamone, Teresa Santangelo, Luigia Scudeller, Luca Saba, Paolo Tomà, Giovanni Morana
Publikováno v:
European Respiratory Review, Vol 31, Iss 163 (2022)
Objective Imaging represents an important noninvasive means to assess cystic fibrosis (CF) lung disease, which remains the main cause of morbidity and mortality in CF patients. While the development of new imaging techniques has revolutionised clinic
Externí odkaz:
https://doaj.org/article/fd30fd88416348f3902a7bc54661e9bd
Autor:
Michela Francalanci, Vito Terlizzi, Cristina Fevola, Giulia Di Rosa, Valentina Pierattini, Elena Roselli, Paolo Bonomi, Maria Chiara Cavicchi, Valeria Galici, Anna Silvia Neri, Chiara Bianchimani, Silvia Campana, Daniela Dolce, Novella Ravenni, Erica Camera, Tommaso Orioli, Giovanni Taccetti
Publikováno v:
Children, Vol 10, Iss 2, p 252 (2023)
Background: Improved therapy in CF has led to an overall improvement in nutritional status. The objectives of our study are: to cross-sectionally assess nutritional status and serum levels of fat-soluble vitamins; to retrospectively evaluate the effi
Externí odkaz:
https://doaj.org/article/efeed00c31eb4d6f93d955d8673fb593
Autor:
Giovanni Taccetti, Matteo Botti, Vito Terlizzi, Maria Chiara Cavicchi, Anna Silvia Neri, Valeria Galici, Gianfranco Mergni, Claudia Centrone, Diego G. Peroni, Filippo Festini
Publikováno v:
Diagnostics, Vol 10, Iss 7, p 446 (2020)
Cystic fibrosis (CF) is a life-threatening and common genetic disorder. Cystic fibrosis newborn screening (CF NBS) has been implemented in many countries over the last 30 years, becoming a widely accepted public health strategy in economically develo
Externí odkaz:
https://doaj.org/article/0824c7c6bec44137ba3c47226339f538
Autor:
Letizia Macconi, Valeria Galici, Marco Di Maurizio, Enrica Rossi, Giovanni Taccetti, Vito Terlizzi
Publikováno v:
Journal of Clinical Medicine. 11:4277
This is a prospective, observational study involving three Cystic Fibrosis (CF) adult patients, evaluating the changes in chest magnetic resonance imaging (MRI) three months after the start of elexacaftor/tezacaftor and ivacaftor therapy. MRI showed
Autor:
Valeria Galici, Maria Chiara Cavicchi, Anna Silvia Neri, Matteo Botti, C. Centrone, G. Mergni, Vito Terlizzi, Giovanni Taccetti, Lucia Zavataro, Daniela Dolce, Michela Francalanci, Filippo Festini
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-8 (2021)
BackgroundCystic fibrosis (CF) is a life-threatening disease affecting about 1:3000 newborns in Caucasian populations. The introduction of newborn screening for cystic fibrosis (CF NBS) has improved the clinical outcomes of individuals with CF throug
Publikováno v:
Nutrition in Clinical Practice. 36:907-908
Autor:
Vito Terlizzi, Valeria Galici, Anna Silvia Neri, G. Mergni, C. Centrone, Diego Peroni, Giovanni Taccetti, Maria Chiara Cavicchi, Filippo Festini, Matteo Botti
Publikováno v:
Diagnostics, Vol 10, Iss 446, p 446 (2020)
Diagnostics
Volume 10
Issue 7
Diagnostics
Volume 10
Issue 7
Cystic fibrosis (CF) is a life-threatening and common genetic disorder. Cystic fibrosis newborn screening (CF NBS) has been implemented in many countries over the last 30 years, becoming a widely accepted public health strategy in economically develo