P. Buonpensiero

Short-term effects on tolerability of inhaled hypertonic saline solution and hypertonic saline plus hyaluronic acid in cystic fibrosis patients

V. Raia, A. Tosco, A. Pasqua, 2014 .

Burkholderia cepacia complex infection in a cohort of Italian patients with cystic fibrosis.

V. Raia, S. Stefani, A. Lambiase, 2007, Journal of microbiology.

Noninvasive Ventilation and Pulmonary Rehabilitation

P. Buonpensiero, 2020 .

High flow oxygen therapy and the work of breathing assessed by thickening fraction of the diaphragm (TFdi): just a side of the moon in cystic fibrosis patients?

A. Esquinas, N. Corcione, P. Buonpensiero, 2019, Annals of translational medicine.

Home physiotherapists assisting follow-up treatment in cystic fibrosis: a multicenter observational study.

M. Ros, A. Orenti, P. Buonpensiero, 2021, Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace.

Ursodeoxycholic acid treatment in patients with cystic fibrosis at risk for liver disease.

V. Raia, B. Boggia, M. Siano, 2010, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Hyaluronic acid improves “pleasantness” and tolerability of nebulized hypertonic saline in a cohort of patients with cystic fibrosis

V. Raia, M. Siano, A. Pasqua, 2010, Advances in therapy.

A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

M. Maiuri, G. Kroemer, G. Stoll, 2016, Cell Death and Differentiation.

A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR

M. Maiuri, G. Kroemer, G. De Rosa, 2016, Cell Death and Differentiation.

The Role of Bronchoscopy in the Management of Children With Cystic Fibrosis

R. Badolato, V. Raia, A. Castaldo, 2022, Journal of bronchology & interventional pulmonology.

Randomized, single blind, controlled trial of inhaled glutathione vs placebo in patients with cystic fibrosis.

P. Abete, V. Raia, V. Carnovale, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A missing early diagnosis of cystic fibrosis associated with a milder phenotype

V. Raia, M. Siano, F. Majo, 2008 .

51 Inhaled GSH tolerability in patients with cystic fibrosis (CF)

V. Raia, V. Carnovale, A. Tosco, 2012 .