DE GREGORIO, FABIOLA
DE GREGORIO, FABIOLA
Sphingobacterium respiratory tract infection in patients with cystic fibrosis.
2009 Lambiase, A.; Rossano, Fabio; DEL PEZZO, Mariassunta; Raia, Valeria; Sepe, A.; DE GREGORIO, Fabiola; Catania, MARIA ROSARIA
Hyaluronic acid improves "pleasantness" and tolerability of nebulized hypertonic saline in a cohort of patients with cystic fibrosis
2010 Buonpensiero, Paolo; DE GREGORIO, Fabiola; Sepe, Angela; Di Pasqua, A; Ferri, Pasqualina; Siano, Maria; Terlizzi, Vito; Raia, Valeria
Ursodeoxycholic acid treatment in patients with cystic fibrosis at risk for liver disease
2010 Siano, Maria; DE GREGORIO, Fabiola; Boggia, Bartolomeo; Sepe, Angela; Ferri, Pasqualina; Buonpensiero, Paolo; Di Pasqua, A; Raia, Valeria
Brand new SPINK1 and CFTR mutations in a child with acute recurrent pancreatitis: a case report.
2013 Terlizzi, Vito; DE GREGORIO, Fabiola; Sepe, A; Amato, N; Arduino, C; Casale, A; Majo, Fabio; Tomaiuolo, Rossella; Castaldo, Giuseppe; Raia, Valeria
Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study
2017 Maglione, Marco; Montella, Silvia; Mollica, Carmine; Carnovale, Vincenzo; Iacotucci, Paola; DE GREGORIO, Fabiola; Tosco, Antonella; Cervasio, Mariarosaria; Raia, Valeria; Santamaria, Francesca
Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation
2017 Ferrari, Eleonora; Monzani, Romina; Villella, VALERIA RACHELA; Esposito, Speranza; Saluzzo, Francesca; Rossin, Federica; D'Eletto, Manuela; Tosco, Antonella; DE GREGORIO, Fabiola; Izzo, Valentina; Maiuri, MARIA CHIARA; Kroemer, Guido; Raia, Valeria; Maiuri, Luigi
Intra-individual biological variation in sweat chloride concentrations in CF, CFTR dysfunction, and healthy pediatric subjects
2018 Cirilli, Natalia; Raia, Valeria; Rocco, Ilaria; De Gregorio, Fabiola; Tosco, Antonella; Salvadori, Laura; Sepe, Angela Ornella; Buzzetti, Roberto; Minicuci, Nadia; Castaldo, Giuseppe
Effectiveness and safety of elexacaftor/tezacaftor/ivacaftor in patients with cystic fibrosis and advanced lung disease with the Phe508del/minimal function genotype
2021 Carnovale, Vincenzo; Iacotucci, Paola; Terlizzi, Vito; Colangelo, Carmela; Medio, Pietro; Ferrillo, Lorenza; De Gregorio, Fabiola; Francalanci, Michela; Taccetti, Giovanni; Buonaurio, Serena; D'Ippolito, Marcella; Marsicovetere, Giovanni; D'Andria, Michele; Ferrara, Nicola; Salvatore, Donatello
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Sphingobacterium respiratory tract infection in patients with cystic fibrosis. | 1.1 Articolo in rivista | 2009 | Lambiase, A.; Rossano, Fabio; DEL PEZZO, Mariassunta; Raia, Valeria; Sepe, A.; DE GREGORIO, Fabiola; Catania, MARIA ROSARIA | |
| Hyaluronic acid improves "pleasantness" and tolerability of nebulized hypertonic saline in a cohort of patients with cystic fibrosis | 1.1 Articolo in rivista | 2010 | Buonpensiero, Paolo; DE GREGORIO, Fabiola; Sepe, Angela; Di Pasqua, A; Ferri, Pasqualina; Siano, Maria; Terlizzi, Vito; Raia, Valeria | |
| Ursodeoxycholic acid treatment in patients with cystic fibrosis at risk for liver disease | 1.1 Articolo in rivista | 2010 | Siano, Maria; DE GREGORIO, Fabiola; Boggia, Bartolomeo; Sepe, Angela; Ferri, Pasqualina; Buonpensiero, Paolo; Di Pasqua, A; Raia, Valeria | |
| Brand new SPINK1 and CFTR mutations in a child with acute recurrent pancreatitis: a case report. | 1.1 Articolo in rivista | 2013 | Terlizzi, Vito; DE GREGORIO, Fabiola; Sepe, A; Amato, N; Arduino, C; Casale, A; Majo, Fabio; Tomaiuolo, Rossella; Castaldo, Giuseppe; Raia, Valeria | |
| Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study | 1.1 Articolo in rivista | 2017 | Maglione, Marco; Montella, Silvia; Mollica, Carmine; Carnovale, Vincenzo; Iacotucci, Paola; DE GREGORIO, Fabiola; Tosco, Antonella; Cervasio, Mariarosaria; Raia, Valeria; Santamaria, Francesca | |
| Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation | 1.1 Articolo in rivista | 2017 | Ferrari, Eleonora; Monzani, Romina; Villella, VALERIA RACHELA; Esposito, Speranza; Saluzzo, Francesca; Rossin, Federica; D'Eletto, Manuela; Tosco, Antonella; DE GREGORIO, Fabiola; Izzo, Valentina; Maiuri, MARIA CHIARA; Kroemer, Guido; Raia, Valeria; Maiuri, Luigi | |
| Intra-individual biological variation in sweat chloride concentrations in CF, CFTR dysfunction, and healthy pediatric subjects | 1.1 Articolo in rivista | 2018 | Cirilli, Natalia; Raia, Valeria; Rocco, Ilaria; De Gregorio, Fabiola; Tosco, Antonella; Salvadori, Laura; Sepe, Angela Ornella; Buzzetti, Roberto; Minicuci, Nadia; Castaldo, Giuseppe | |
| Effectiveness and safety of elexacaftor/tezacaftor/ivacaftor in patients with cystic fibrosis and advanced lung disease with the Phe508del/minimal function genotype | 1.1 Articolo in rivista | 2021 | Carnovale, Vincenzo; Iacotucci, Paola; Terlizzi, Vito; Colangelo, Carmela; Medio, Pietro; Ferrillo, Lorenza; De Gregorio, Fabiola; Francalanci, Michela; Taccetti, Giovanni; Buonaurio, Serena; D'Ippolito, Marcella; Marsicovetere, Giovanni; D'Andria, Michele; Ferrara, Nicola; Salvatore, Donatello |