NANETTI, LORENZO
NANETTI, LORENZO
Universita' degli Studi di MILANO
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
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
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
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