1. A previously undescribed de novo insertion-deletion mutation in the beta myosin heavy chain gene in a kindred with familial hypertrophic cardiomyopathy. Issue 5 (November 1996) Authors: Cuda, G.; Perrotti, N.; Perticone, F.; Mattioli, P. L. Journal: Heart Issue: Volume 76:Issue 5(1996) Page Start: 451 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Proteomics‐Driven Assay Defines Specific Plasma Protein Signatures in Different Stages of Ménière's Disease. Issue 6 (June 2014) Authors: Chiarella, G.; Di Domenico, M.; Petrolo, C.; Saccomanno, M.; Rothenberger, R.; Giordano, A.; Costanzo, F.; Cassandro, E.; Cuda, G. Journal: Journal of cellular biochemistry Issue: Volume 115:Issue 6(2014:Jun.) Page Start: 1097 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Superhydrophobic lab-on-chip measures secretome protonation state and provides a personalized risk assessment of sporadic tumour. Issue 1 (December 2018) Authors: Malara, N.; Gentile, F.; Coppedè, N.; Coluccio, M.; Candeloro, P.; Perozziello, G.; Ferrara, L.; Giannetto, M.; Careri, M.; Castellini, A.; Mignogna, C.; Presta, I.; Pirrone, C.; Maisano, D.; Donato, A.; Donato, G.; Greco, M.; Scumaci, D.; Cuda, G.; Casale, F. Journal: Npj precision oncology Issue: Volume 2:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗