TRITTO, VIVIANA
TRITTO, VIVIANA
Dipartimento di Medicina Molecolare e Traslazionale
Alteration of RAS pathway phosphorylation in Noonan syndrome patients carrying hypomorphic variants in two NS genes
2024-01-01 Tritto, Viviana; Capitanio, Daniele; Gelfi, Cecilia; Riva, Paola
Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR
2024-01-01 Bettinaglio, Paola; Tritto, Viviana; Paterra, Rosina; Eoli, Marica; Riva, Paola
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes
2024-01-01 Tritto, Viviana; Bettinaglio, Paola; Mangano, Eleonora; Cesaretti, Claudia; Marasca, Federica; Castronovo, Chiara; Bordoni, Roberta; Battaglia, Cristina; Saletti, Veronica; Ranzani, Valeria; Bodega, Beatrice; Eoli, Marica; Natacci, Federica; Riva, Paola
Natural history of spinal involvement in Neurofibromatosis type 1: clues from "reverse follow-up"
2024-01-01 Cesaretti, Claudia; Conti, Beatrice; Grilli, Federico; Casale, Silvia; Riva, Paola; Tritto, Viviana; Cristina Ibba, Maria; Valentina Genovese, Antonia; Sciacco, Monica; Caroli, Manuela; Eoli, Marica; Avignone, Sabrina; Natacci, Federica
NF1 Gene Mutation Mediates Neuronal Signaling De-Regulation Triggering Pediatric Optic Glioma Development: Another Small Step towards a Cure of NF1 Disorder?
2021-01-01 Riva, Paola Vanda; Tritto, Viviana
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
2024-01-01 Redaelli, Serena; Romana Grati, Francesca; Tritto, Viviana; Giannuzzi, Giuliana; Paola Recalcati, Maria; Sala, Elena; Villa, Nicoletta; Crosti, Francesca; Roversi, Gaia; Malvestiti, Francesca; Zanatta, Valentina; Repetti, Elena; Rodeschini, Ornella; Valtorta, Chiara; Catusi, Ilaria; Romitti, Lorenza; Martinoli, Emanuela; Conconi, Donatella; Dalpra`, Leda; Lavitrano, Marialuisa; Riva, Paola; Bentivegna, Angela
Phenotypic variability in rare NF2 patients carrying 22q12 microdeletions: exploring genetic and epigenetic mechanisms
2024-01-01 Tritto, Viviana; Pozzi, Micol; Paterra, Rosina; Borghi, Arianna; Redaelli, Serena; Eoli, Marica; Riva, Paola
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Alteration of RAS pathway phosphorylation in Noonan syndrome patients carrying hypomorphic variants in two NS genes | 1-gen-2024 | Tritto, Viviana; Capitanio, Daniele; Gelfi, Cecilia; Riva, Paola | |
| Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR | 1-gen-2024 | Bettinaglio, Paola; Tritto, Viviana; Paterra, Rosina; Eoli, Marica; Riva, Paola | |
| Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes | 1-gen-2024 | Tritto, Viviana; Bettinaglio, Paola; Mangano, Eleonora; Cesaretti, Claudia; Marasca, Federica; Castronovo, Chiara; Bordoni, Roberta; Battaglia, Cristina; Saletti, Veronica; Ranzani, Valeria; Bodega, Beatrice; Eoli, Marica; Natacci, Federica; Riva, Paola | |
| Natural history of spinal involvement in Neurofibromatosis type 1: clues from "reverse follow-up" | 1-gen-2024 | Cesaretti, Claudia; Conti, Beatrice; Grilli, Federico; Casale, Silvia; Riva, Paola; Tritto, Viviana; Cristina Ibba, Maria; Valentina Genovese, Antonia; Sciacco, Monica; Caroli, Manuela; Eoli, Marica; Avignone, Sabrina; Natacci, Federica | |
| NF1 Gene Mutation Mediates Neuronal Signaling De-Regulation Triggering Pediatric Optic Glioma Development: Another Small Step towards a Cure of NF1 Disorder? | 1-gen-2021 | Riva, Paola Vanda; Tritto, Viviana | |
| Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators? | 1-gen-2024 | Redaelli, Serena; Romana Grati, Francesca; Tritto, Viviana; Giannuzzi, Giuliana; Paola Recalcati, Maria; Sala, Elena; Villa, Nicoletta; Crosti, Francesca; Roversi, Gaia; Malvestiti, Francesca; Zanatta, Valentina; Repetti, Elena; Rodeschini, Ornella; Valtorta, Chiara; Catusi, Ilaria; Romitti, Lorenza; Martinoli, Emanuela; Conconi, Donatella; Dalpra`, Leda; Lavitrano, Marialuisa; Riva, Paola; Bentivegna, Angela | |
| Phenotypic variability in rare NF2 patients carrying 22q12 microdeletions: exploring genetic and epigenetic mechanisms | 1-gen-2024 | Tritto, Viviana; Pozzi, Micol; Paterra, Rosina; Borghi, Arianna; Redaelli, Serena; Eoli, Marica; Riva, Paola |