VASTA, ROBERTA GIOVANNA
VASTA, ROBERTA GIOVANNA
Universita' degli Studi di MILANO
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes
2025 A. Manini, A. Brusati, M. Grassano, G. Scacciatella, S. Peverelli, J. Spagliardi, V. Pensato, A. Doretti, R. Vasta, U. Manera, A. Canosa, M. Brunetti, D. Gentilini, S. Messina, F. Verde, C. Moglia, C. Morelli, E. Dalla Bella, P.J. Keagle, J.E. Landers, C. Gellera, G. Lauria Pinter, A. Chio, A. Ratti, A. Calvo, V. Silani, N. Ticozzi
The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment
2021 P. Lanteri, I. Meola, A. Canosa, G. De Marco, A. Lomartire, M. Rinaudo, E. Albamonte, V. Sansone, C. Lunetta, U. Manera, R. Vasta, C. Moglia, A. Calvo, P. Origone, A. Chio, P. Mandich
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes | 2025 | Manini A.Scacciatella G.Peverelli S.Spagliardi J.Pensato V.Doretti A.Vasta R.Gentilini D.Verde F.Lauria Pinter G.Ratti A.Silani V.Ticozzi N. + | Article (author) | - | |
| The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairment | 2021 | Lanteri PDe Marco GSansone VAVasta R + | Article (author) | - |