L. Zazzeron

Identification of insulin secretory defects and insulin resistance during oral glucose tolerance test in a cohort of cystic fibrosis patients.

A. Battezzati, A. Mari, C. Colombo, 2011, European journal of endocrinology.

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.

Dietary and Circulating Polyunsaturated Fatty Acids in Cystic Fibrosis: Are They Related to Clinical Outcomes?

C. Agostoni, C. Colombo, E. Riva, 2006, Journal of pediatric gastroenterology and nutrition.

Benefits of breastfeeding in cystic fibrosis: A single‐centre follow‐up survey

C. Agostoni, C. Colombo, E. Riva, 2007, Acta paediatrica.

Effects of prolonged proton pump inhibitor treatment on nutritional status and respiratory infection risk in cystic fibrosis: A matched cohort study.

C. Colombo, F. Corti, V. Daccó, 2022, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Change in Nutrient and Dietary Intake in European Children with Cystic Fibrosis after a 6-Month Intervention with a Self-Management mHealth Tool

M. Boon, C. Ribes-Koninckx, K. De Boeck, 2021, Nutrients.

Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)

M. Seia, C. Colombo, D. Coviello, 2007, European Journal of Human Genetics.

Spontaneous hypoglycemia in patients with cystic fibrosis.

A. Battezzati, S. Bertoli, M. Seia, 2007, European journal of endocrinology.

Ictal video-electroencephalogram of breath-holding attack.

P. Striano, S. Barbieri, R. Dilena, 2023, Journal of Paediatrics and Child Health.

Night Blindness in Cystic Fibrosis: The Key Role of Vitamin A in the Digestive System

C. Colombo, L. Claut, A. Biffi, 2019, Nutrients.

Age- and Sex-Dependent Distribution of OGTT-Related Variables in a Population of Cystic Fibrosis Patients.

G. Bedogni, A. Battezzati, S. Bertoli, 2015, The Journal of clinical endocrinology and metabolism.

Contribution of defects in insulin sensitivity and beta-cell function to the changes over time in the glucose tolerance of cystic fibrosis patients

A. Battezzati, A. Mari, C. Colombo, 2006 .

Effects of insulin therapy optimization with sensor augmented pumps on glycemic control and body composition in people with cystic fibrosis-related diabetes

V. Grancini, A. Gramegna, C. Piona, 2023, Frontiers in endocrinology.