1. Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study. (March 2021) Authors: Suppiej, A.; Ceccato, C.; Maritan, V.; Cermakova, I.; Colavito, D.; Leon, A. Journal: European journal of paediatric neurology Issue: Volume 31(2021) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. P033 Syndromic paucity of intralobular bile ducts secondary to HNF1β-MODY syndrome … not only Alagille syndrome. Issue 4 (6th October 2018) Authors: Pinon, M.; Pizzol, A.; David, E.; Colavito, D.; Calvo, P.L. Journal: Digestive and liver disease Issue: Volume 50:Issue 4(2018)Supplement Page Start: e370 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical application of next generation sequencing for the diagnosis of pediatric hepatic and intestinal diseases: Results of a single centre experience. (10th October 2016) Authors: Cananzi, M.; Colavito, D.; Gaio, P.; Del Giudice, E.; Visentin, F.; Ciccone, S.; Dalle Carbonare, M.; Perilongo, G.; Leon, A. Journal: Digestive and liver disease Issue: Volume 48(2016)Supplement 4 Page Start: e257 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗