FERRARI, MAURIZIO
FERRARI, MAURIZIO
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Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches
2018 Di Resta, Chiara; Spiga, Ivana; Presi, Silvia; Merella, Stefania; Pipitone, Giovanni Battista; Manitto, Maria Pia; Querques, Giuseppe; Battaglia Parodi, Maurizio; Ferrari, Maurizio; Carrera, Paola
The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed condition
2018 Solazzo, Andrea; Testa, Francesca; Giovanella, Silvia; Busutti, Marco; Furci, Luciana; Carrera, Paola; Ferrari, Maurizio; Ligabue, Giulia; Mori, Giacomo; Leonelli, Marco; Cappelli, Gianni; Magistroni, Riccardo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches | 1-gen-2018 | Di Resta, Chiara; Spiga, Ivana; Presi, Silvia; Merella, Stefania; Pipitone, Giovanni Battista; Manitto, Maria Pia; Querques, Giuseppe; Battaglia Parodi, Maurizio; Ferrari, Maurizio; Carrera, Paola | |
| The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed condition | 1-gen-2018 | Solazzo, Andrea; Testa, Francesca; Giovanella, Silvia; Busutti, Marco; Furci, Luciana; Carrera, Paola; Ferrari, Maurizio; Ligabue, Giulia; Mori, Giacomo; Leonelli, Marco; Cappelli, Gianni; Magistroni, Riccardo |