FERRARI, MAURIZIO
FERRARI, MAURIZIO
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A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility
2022 F. Esposito, A.M. Osiceanu, M. Sorosina, L. Ottoboni, B. Bollman, S. Santoro, B. Bettegazzi, A. Zauli, F. Clarelli, E. Mascia, A. Calabria, D. Zacchetti, R. Capra, M. Ferrari, P. Provero, D. Lazarevic, D. Cittaro, P. Carrera, N. Patsopoulos, D. Toniolo, A.D. Sadovnick, G. Martino, P.L. De Jager, G. Comi, E. Stupka, C. Vilariño-Güell, L. Piccio, F. Martinelli Boneschi
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns : a pilot study
2015 P. Carrera, C. Di Resta, C. Volonteri, E. Castiglioni, S. Bonfiglio, D. Lazarevic, D. Cittaro, E. Stupka, M. Ferrari, M. Somaschini
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility | 2022 | Esposito, FedericaOttoboni, LindaCalabria, AndreaFerrari, MaurizioComi, GiancarloPiccio, LauraMartinelli Boneschi, Filippo + | Article (author) | - | |
| Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns : a pilot study | 2015 | M. Ferrari + | Article (author) | - |