1. Early markers of Fabry disease revealed by proteomics1. Issue 6 (19th June 2015) Authors: Matafora, V.; Cuccurullo, M.; Beneduci, A.; Petrazzuolo, O.; Simeone, A.; Anastasio, P.; Mignani, R.; Feriozzi, S.; Pisani, A.; Comotti, C.; Bachi, A.; Capasso, G. Journal: Molecular bioSystems Issue: Volume 11:Issue 6(2015:Jun.) Page Start: 1543 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases. (17th October 2013) Authors: Fallerini, C.; Dosa, L.; Tita, R.; Del Prete, D.; Feriozzi, S.; Gai, G.; Clementi, M.; La Manna, A.; Miglietti, N.; Mancini, R.; Mandrile, G.; Ghiggeri, G.M.; Piaggio, G.; Brancati, F.; Diano, L.; Frate, E.; Pinciaroli, A.R.; Giani, M.; Castorina, P.; Bresin, E. Journal: Clinical genetics Issue: Volume 86:Number 3(2014:Sep.) Page Start: 252 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗