L. Termini

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

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

A polymorphism in the 5’ UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients

A. Covone, R. Ravazzolo, P. Gasparini, 2011, Clinical chemistry and laboratory medicine.

Nebulized hypertonic saline containing hyaluronic acid improves tolerability in patients with cystic fibrosis and lung disease compared with nebulized hypertonic saline alone: a prospective, randomized, double-blind, controlled study

M. Collura, M. Furnari, L. Termini, 2012, Therapeutic advances in respiratory disease.

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.

Stunting is an independent predictor of mortality in patients with cystic fibrosis.

G. Trimarchi, G. Magazzù, S. Pellegrino, 2013, Clinical nutrition.