1. A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy. Issue 11 (16th October 2007) Authors: Muglia, M; Vazza, G; Patitucci, A; Milani, M; Pareyson, D; Taroni, F; Quattrone, A; Mostacciuolo, M L Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 78:Issue 11(2007) Page Start: 1286 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1. Issue 6 (1st June 2002) Authors: Zortea, M; Vettori, A; Trevisan, C P; Bellini, S; Vazza, G; Armani, M; Simonati, A; Mostacciuolo, M L Journal: Journal of medical genetics Issue: Volume 39:Issue 6(2002) Page Start: 387 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The GIP/GIPR axis is functionally linked to GH-secretion increase in a significant proportion of gsp− somatotropinomas. Issue 5 (May 2017) Authors: Regazzo, D; Losa, M; Albiger, N M; Terreni, M R; Vazza, G; Ceccato, F; Emanuelli, E; Denaro, L; Scaroni, C; Occhi, G Journal: European journal of endocrinology Issue: Volume 176:Issue 5(2017) Page Start: 543 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗