NANETTI, LORENZO
NANETTI, LORENZO
Universita' degli Studi di MILANO
A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in Childhood
2024 G. Ferrera, R. Izzo, D. Ghezzi, L. Nanetti, E. Lamantea, A. Ardissone
Oropharyngeal Dysphagia Phenotypes Across Huntington’s Disease Stages: Endoscopic Findings and Tongue Pressure Analysis
2024 N. Pizzorni, A. Ciammola, C. Pirola, L. Nanetti, A. Castaldo, B. Poletti, C. Mariotti, A. Schindler
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies
2024 D. Sala, S. Marchet, L. Nanetti, A. Legati, C. Mariotti, E. Lamantea, D. Ghezzi, A. Catania, C. Lamperti
Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders
2024 M. Cozzi, S. Magri, B. Tedesco, G. Patelli, V. Ferrari, E. Casarotto, M. Chierichetti, P. Pramaggiore, L. Cornaggia, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, J. Mandrioli, D. Pareyson, C. Pisciotta, S. D'Arrigo, A. Ratti, L. Nanetti, C. Mariotti, E. Sarto, V. Pensato, C. Gellera, D. Di Bella, R.M. Cristofani, F. Taroni, A. Poletti
In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients
2020 E. Pozzi, E. Giorgio, C. Mancini, N. Lo Buono, S. Augeri, M. Ferrero, E. Di Gregorio, E. Riberi, M. Vinciguerra, L. Nanetti, F.T. Bianchi, M.P. Sassi, V. Costanzo, C. Mariotti, A. Funaro, S. Cavalieri, A. Brusco
Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment
2019 A. Catania, A. Legati, L. Peverelli, L. Nanetti, S. Marchet, N. Zanetti, C. Lamperti, D. Ghezzi