CERRATO, FRANCESCO
CERRATO, FRANCESCO
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Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques
2022-01-01 Carli, D.; Operti, M.; Russo, S.; Cocchi, G.; Milani, D.; Leoni, C.; Prada, E.; Melis, D.; Falco, M.; Spina, J.; Uliana, V.; Sara, O.; Sirchia, F.; Tarani, L.; Macchiaiolo, M.; Cerrato, F.; Sparago, A.; Pignata, L.; Tannorella, P.; Cardaropoli, S.; Bartuli, A.; Riccio, A.; Ferrero, G. B.; Mussa, A.
Integrated Anaerobic–Aerobic Moving Bed Biofilm Reactor and Biochar Adsorption for the Efficient Removal of Organic Matter and Nutrients from Brazilian Landfill Leachate
2023-01-01 Faggiano, Antonio; Motta, Oriana; Ricciardi, Maria; Cerrato, Francesco; Garcia Junior, Carlos Augusto; Fiorentino, Antonino; Proto, Antonio
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
2020-01-01 Cubellis, M. V.; Pignata, L.; Verma, A.; Sparago, A.; Del Prete, R.; Monticelli, M.; Calzari, L.; Antona, V.; Melis, D.; Tenconi, R.; Russo, S.; Cerrato, F.; Riccio, A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques | 1-gen-2022 | Carli, D.; Operti, M.; Russo, S.; Cocchi, G.; Milani, D.; Leoni, C.; Prada, E.; Melis, D.; Falco, M.; Spina, J.; Uliana, V.; Sara, O.; Sirchia, F.; Tarani, L.; Macchiaiolo, M.; Cerrato, F.; Sparago, A.; Pignata, L.; Tannorella, P.; Cardaropoli, S.; Bartuli, A.; Riccio, A.; Ferrero, G. B.; Mussa, A. | |
| Integrated Anaerobic–Aerobic Moving Bed Biofilm Reactor and Biochar Adsorption for the Efficient Removal of Organic Matter and Nutrients from Brazilian Landfill Leachate | 1-gen-2023 | Faggiano, Antonio; Motta, Oriana; Ricciardi, Maria; Cerrato, Francesco; Garcia Junior, Carlos Augusto; Fiorentino, Antonino; Proto, Antonio | |
| Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance | 1-gen-2020 | Cubellis, M. V.; Pignata, L.; Verma, A.; Sparago, A.; Del Prete, R.; Monticelli, M.; Calzari, L.; Antona, V.; Melis, D.; Tenconi, R.; Russo, S.; Cerrato, F.; Riccio, A. |