Novelli, Antonio
Novelli, Antonio
Clinical characteristics and risk of arrhythmic events in patients younger than 12 years diagnosed with Brugada syndrome
2021-01-01 Righi, Daniela; Porco, Luigina; Calvieri, Camilla; Tamborrino, Pietro Paolo; Di Mambro, Corrado; Paglia, Simone; Baban, Anwar; Silvetti, Massimo Stefano; Gnazzo, Maria; Novelli, Antonio; Tozzi, Alberto Eugenio; Drago, Fabrizio
COL1-related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap
2020-01-01 Morlino, S.; Micale, L.; Ritelli, M.; Rohrbach, M.; Zoppi, N.; Vandersteen, A.; Mackay, S.; Agolini, E.; Cocciadiferro, D.; Sasaki, E.; Madeo, A.; Ferraris, A.; Reardon, W.; Di Rocco, M.; Novelli, Antonio; Grammatico, P.; Malfait, F.; Mazza, T.; Hakim, A.; Giunta, C.; Colombi, M.; Castori, M.
COVID-19: S-Peptide RBD 484–508 Induces IFN-γ T-Cell Response in Naïve-to-Infection and Unvaccinated Subjects with Close Contact with SARS-CoV-2-Positive Patients
2023-01-01 Murdocca, Michela; Citro, Gennaro; Centanini, Eleonora; Giannini, Rosalinda; Latini, Andrea; Centofanti, Federica; Piano Mortari, Eva; Cocciadiferro, Dario; Novelli, Antonio; Bernardini, Sergio; Novelli, Giuseppe; Sangiuolo, Federica
COVID‐19 and genetic variants of protein involved in the SARS‐CoV‐2 entry into the host cells
2020-01-01 Latini, Andrea; Agolini, Emanuele; Novelli, Antonio; Borgiani, Paola; Giannini, Rosalinda; Gravina, Paolo; Smarrazzo, Andrea; Dauri, Mario; Andreoni, Massimo; Rogliani, Paola; Bernardini, Sergio; Helmer‐citterich, Manuela; Biancolella, Michela; Novelli, Giuseppe
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions
2013-01-01 Ferraris, A.; Bernardini, L.; Avramovska, V. S.; Zanni, G.; Loddo, S.; Sukarova-Angelovska, E.; Parisi, V.; Capalbo, A.; Tumini, S.; Travaglini, L.; Mancini, F.; Duma, F.; Barresi, S.; Novelli, Antonio; Mercuri, E.; Tarani, L.; Bertini, E.; Dallapiccola, B.; Valente, E. M.
Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors
2022-01-01 Latini, Andrea; Vancheri, Chiara; Amati, Francesca; Morini, Elena; Grelli, Sandro; Claudia, Matteucci; Vita, Petrone; Colona, Vito Luigi; Murdocca, Michela; Andreoni, Massimo; Malagnino, Vincenzo; Raponi, Massimiliano; Cocciadiferro, Dario; Novelli, Antonio; Borgiani, Paola; Novelli, Giuseppe
GRIA3 missense mutation is cause of an x-linked developmental and epileptic encephalopathy
2020-01-01 Trivisano, Marina; Santarone, Marta Elena; Micalizzi, Alessia; Ferretti, Alessandro; Dentici, Maria Lisa; Novelli, Antonio; Vigevano, Federico; Specchio, Nicola
HLA-haploidentical TCR alpha beta(+)/CD19(+)-depleted stem cell transplantation in children and young adults with Fanconi anemia
2021-01-01 Strocchio, L.; Pagliara, D.; Algeri, M.; Li Pira, G.; Rossi, F.; Bertaina, V.; Leone, G.; Pinto, R. M.; Andreani, M.; Agolini, E.; Girardi, K.; Gaspari, S.; Grapulin, L.; Del Bufalo, F.; Novelli, A.; Merli, Pietro; Locatelli, F.
THE DISCOVERY OF A NOVEL GENETIC MUTATION IN BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS WIDENS THE INSIGHTS INTO DISORDER RELATED-MOLECULAR ANALYSIS
2019-01-01 Piazzolla, M.; Castellaneta, N. M.; Novelli, Antonio; Agolini, E.; Cocciadiferro, D.; Resta, L.; Ierardi, E.; Di Leo, A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical characteristics and risk of arrhythmic events in patients younger than 12 years diagnosed with Brugada syndrome | 1-gen-2021 | Righi, Daniela; Porco, Luigina; Calvieri, Camilla; Tamborrino, Pietro Paolo; Di Mambro, Corrado; Paglia, Simone; Baban, Anwar; Silvetti, Massimo Stefano; Gnazzo, Maria; Novelli, Antonio; Tozzi, Alberto Eugenio; Drago, Fabrizio | |
| COL1-related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers-Danlos syndrome overlap | 1-gen-2020 | Morlino, S.; Micale, L.; Ritelli, M.; Rohrbach, M.; Zoppi, N.; Vandersteen, A.; Mackay, S.; Agolini, E.; Cocciadiferro, D.; Sasaki, E.; Madeo, A.; Ferraris, A.; Reardon, W.; Di Rocco, M.; Novelli, Antonio; Grammatico, P.; Malfait, F.; Mazza, T.; Hakim, A.; Giunta, C.; Colombi, M.; Castori, M. | |
| COVID-19: S-Peptide RBD 484–508 Induces IFN-γ T-Cell Response in Naïve-to-Infection and Unvaccinated Subjects with Close Contact with SARS-CoV-2-Positive Patients | 1-gen-2023 | Murdocca, Michela; Citro, Gennaro; Centanini, Eleonora; Giannini, Rosalinda; Latini, Andrea; Centofanti, Federica; Piano Mortari, Eva; Cocciadiferro, Dario; Novelli, Antonio; Bernardini, Sergio; Novelli, Giuseppe; Sangiuolo, Federica | |
| COVID‐19 and genetic variants of protein involved in the SARS‐CoV‐2 entry into the host cells | 1-gen-2020 | Latini, Andrea; Agolini, Emanuele; Novelli, Antonio; Borgiani, Paola; Giannini, Rosalinda; Gravina, Paolo; Smarrazzo, Andrea; Dauri, Mario; Andreoni, Massimo; Rogliani, Paola; Bernardini, Sergio; Helmer‐citterich, Manuela; Biancolella, Michela; Novelli, Giuseppe | |
| Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions | 1-gen-2013 | Ferraris, A.; Bernardini, L.; Avramovska, V. S.; Zanni, G.; Loddo, S.; Sukarova-Angelovska, E.; Parisi, V.; Capalbo, A.; Tumini, S.; Travaglini, L.; Mancini, F.; Duma, F.; Barresi, S.; Novelli, Antonio; Mercuri, E.; Tarani, L.; Bertini, E.; Dallapiccola, B.; Valente, E. M. | |
| Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors | 1-gen-2022 | Latini, Andrea; Vancheri, Chiara; Amati, Francesca; Morini, Elena; Grelli, Sandro; Claudia, Matteucci; Vita, Petrone; Colona, Vito Luigi; Murdocca, Michela; Andreoni, Massimo; Malagnino, Vincenzo; Raponi, Massimiliano; Cocciadiferro, Dario; Novelli, Antonio; Borgiani, Paola; Novelli, Giuseppe | |
| GRIA3 missense mutation is cause of an x-linked developmental and epileptic encephalopathy | 1-gen-2020 | Trivisano, Marina; Santarone, Marta Elena; Micalizzi, Alessia; Ferretti, Alessandro; Dentici, Maria Lisa; Novelli, Antonio; Vigevano, Federico; Specchio, Nicola | |
| HLA-haploidentical TCR alpha beta(+)/CD19(+)-depleted stem cell transplantation in children and young adults with Fanconi anemia | 1-gen-2021 | Strocchio, L.; Pagliara, D.; Algeri, M.; Li Pira, G.; Rossi, F.; Bertaina, V.; Leone, G.; Pinto, R. M.; Andreani, M.; Agolini, E.; Girardi, K.; Gaspari, S.; Grapulin, L.; Del Bufalo, F.; Novelli, A.; Merli, Pietro; Locatelli, F. | |
| THE DISCOVERY OF A NOVEL GENETIC MUTATION IN BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS WIDENS THE INSIGHTS INTO DISORDER RELATED-MOLECULAR ANALYSIS | 1-gen-2019 | Piazzolla, M.; Castellaneta, N. M.; Novelli, Antonio; Agolini, E.; Cocciadiferro, D.; Resta, L.; Ierardi, E.; Di Leo, A. |