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Minerva Pediatrica|February 15, 2019
Inhaled medications in cystic fibrosis beyond antibioticsAngela Sepe, Valeria R Villella, Chiara Cimbalo, et al.
Scientific Reports|April 8, 2022
Oxylipin profile in saliva from patients with cystic fibrosis reveals a balance between pro-resolving and pro-inflammatory moleculesVincenzo Carnovale, Alice Castaldo, Alessandro Di Minno, et al.
Diagnostics (Basel, Switzerland)|April 25, 2020
Salivary Cytokines and Airways Disease Severity in Patients with Cystic FibrosisAlice Castaldo, Paola Iacotucci, Vincenzo Carnovale, et al.
Clinical Case Reports|November 29, 2023
Pseudo-Bartter syndrome in infant with cystic fibrosis screen positive, inconclusive diagnosis: A case reportAngela Sepe, Camilla Romano, Ivana Landi, et al.
Pulmonary Pharmacology & Therapeutics|August 20, 2025
Exploring the role of β2- and β3-adrenergic receptors in cystic fibrosisAlessandro Cannavo, Marika Comegna, Alice Castaldo, et al.
Translational Pediatrics|January 3, 2022
Non-invasive tools for detection of liver disease in children and adolescents with cystic fibrosisAntonella Tosco, Angela Sepe, Alice Castaldo, et al.
Plos One|January 7, 2021
Impaired cholesterol metabolism in the mouse model of cystic fibrosis. A preliminary studyFelice Amato, Alice Castaldo, Giuseppe Castaldo, et al.
Journal of Clinical Medicine|April 12, 2025
Tracheal Diverticula in People with Cystic Fibrosis on Elexacaftor/Tezacaftor/Ivacaftor: An Italian Multicenter Retrospective StudyLaura Venditto, Antonella Tosco, Angela Sepe, et al.
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