A. D. di Lullo

S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy

V. Raia, G. Castaldo, A. D. Di Lullo, 2018, Italian Journal of Pediatrics.

Strategy for the treatment and follow-up of sinonasal solitary extramedullary plasmacytoma: a case series

E. Cantone, M. Iengo, E. Guadagno, 2017, Journal of Medical Case Reports.

Clinical expression of cystic fibrosis in a large cohort of Italian siblings

V. Raia, M. Lucarelli, V. Carnovale, 2018, BMC Pulmonary Medicine.

Two CFTR mutations within codon 970 differently impact on the chloride channel functionality

G. Castaldo, A. D. Di Lullo, C. Braggion, 2019, Human mutation.

An "ex vivo model" contributing to the diagnosis and evaluation of new drugs in cystic fibrosis

V. Raia, L. Maiuri, G. Castaldo, 2017, Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale.

Apparent diffusion coefficients for predicting primary cholesteatoma risk of recurrence after surgical clearance.

Andrea Elefante, Arturo Brunetti, A. Brunetti, 2020, European journal of radiology.

Diagnosis and management of intralabyrinthine schwannoma: case series and review of the literature

E. Cantone, L. Brunese, F. Tortora, 2020, Acta bio-medica : Atenei Parmensis.

Assisting PNA transport through cystic fibrosis human airway epithelia with biodegradable hybrid lipid-polymer nanoparticles

F. Ungaro, G. Castaldo, I. d’Angelo, 2020, Scientific Reports.

Cystic Fibrosis: The Sense of Smell

V. Carnovale, P. Iacotucci, G. Castaldo, 2020, American journal of rhinology & allergy.

Abstracts from the 23rd Italian congress of Cystic Fibrosis and the 13th National congress of Cystic Fibrosis Italian Society

N. Segata, F. Armanini, P. Palange, 2018, Italian Journal of Pediatrics.

Unusual Localization of an Emergent Bacterium, Raoultella ornithinolytica

E. Cantone, M. Iengo, M. Cavaliere, 2020, Case reports in medicine.