Sphingobacterium respiratory tract infection in patients with cystic fibrosis

Por Lambiase, Antonietta, Rossano, Fabio, Del Pezzo, Mariassunta, Raia, Valeria, Sepe, Angela, de Gregorio, Fabiola, Catania, Maria Rosaria
Publicado em 2009

Glucose Derangements in Very Young Children With Cystic Fibrosis and Pancreatic Insufficiency

Por Mozzillo, Enza, Raia, Valeria, Fattorusso, Valentina, Falco, Mariateresa, Sepe, Angela, De Gregorio, Fabiola, Nugnes, Rosa, Valerio, Giuliana, Franzese, Adriana
Publicado em 2012

Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study

Por Maglione, Marco, Montella, Silvia, Mollica, Carmine, Carnovale, Vincenzo, Iacotucci, Paola, De Gregorio, Fabiola, Tosco, Antonella, Cervasio, Mariarosaria, Raia, Valeria, Santamaria, Francesca
Publicado no Ital J Pediatr (2017)

Ubiquitin-proteasome-rich cytoplasmic structures in neutrophils of patients with Shwachman-Diamond syndrome

Por Necchi, Vittorio, Minelli, Antonella, Sommi, Patrizia, Vitali, Agostina, Caruso, Roberta, Longoni, Daniela, Frau, Maria Rita, Nasi, Cristina, De Gregorio, Fabiola, Zecca, Marco, Ricci, Vittorio, Danesino, Cesare, Solcia, Enrico
Publicado em 2012

Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation

Por Ferrari, Eleonora, Monzani, Romina, Villella, Valeria R, Esposito, Speranza, Saluzzo, Francesca, Rossin, Federica, D'Eletto, Manuela, Tosco, Antonella, De Gregorio, Fabiola, Izzo, Valentina, Maiuri, Maria C, Kroemer, Guido, Raia, Valeria, Maiuri, Luigi
Publicado no Cell Death Dis (2017)