1. A curious case of hypertransaminasemia. Issue 4 (October 2017) Authors: Pedoto, D.; Di Palma, M.; Di Nuzzi, A.; Cambriglia, D.; Pierri, L.; Vajro, P. Journal: Digestive and liver disease Issue: Volume 49:Issue 4(2017)Supplement Page Start: e256 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Drop-out of obese children in different care settings: Presence of NAFLD complication tends to improve compliance. Issue 4 (October 2017) Authors: Lausi, O.; Belmonte, F.; Bisogno, A.; Di Nuzzi, A.; Delli Bovi, A.P.; Di Michele, L.; Pierri, L.; Annunziata, M.; De Chiara, M.; Fasolino, F.; Pepe, F.M.; Vajro, P. Journal: Digestive and liver disease Issue: Volume 49:Issue 4(2017)Supplement Page Start: e279 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. P048 Metabolomic link between NAFLD and metabolic syndrome in obese children. Issue 4 (6th October 2018) Authors: Troisi, J.; Pierri, L.; Belmonte, F.; Bisogno, A.; Di Nuzzi, A.; De Anseris, A.G.; Di Michele, L.; Delli Bovi, A.P.; Guercio Nuzio, S.; Vajro, P. Journal: Digestive and liver disease Issue: Volume 50:Issue 4(2018)Supplement Page Start: e376 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. P057 Persistent hypertransaminasemia in an obese child with asymptomatic Wilson disease and familiarity for parkinsonism and cardiomyopathy: a case report. Issue 4 (6th October 2018) Authors: Rocco, M.C.; Lettieri, M.; Biffaro, N.; Colantuono, R.; Paglia, P.; Siano, M.A.; Satta, S.; Lepori, M.B.; Loudianos, G.; Mandato, C.; Pacifico, R.; Nazzaro, L.; De Anseris, A.G.E.; Di Nuzzi, A.; Vajro, P. Journal: Digestive and liver disease Issue: Volume 50:Issue 4(2018)Supplement Page Start: e379 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The kidney in Fabry's disease. (30th May 2014) Authors: Pisani, A.; Visciano, B.; Imbriaco, M.; Di Nuzzi, A.; Mancini, A.; Marchetiello, C.; Riccio, E. Journal: Clinical genetics Issue: Volume 86:Number 4(2014:Oct.) Page Start: 301 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Three patients with glycosylation deficiencies, chronically elevated transaminases, and low serum ceruloplasmin and copper, caused by mutations in the gene encoding the transmembrane protein TMEM199. Issue 4 (October 2017) Authors: Poeta, M.; Zielinska, K.; Maccarana, M.; Mandato, C.; Ng, B.G.; Di Nuzzi, A.; D'Acunto, E.; Pierri, L.; Ecklund, E.; Freeze, H.; Vajro, P. Journal: Digestive and liver disease Issue: Volume 49:Issue 4(2017)Supplement Page Start: e249 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗