BAROZZI, SERENA
BAROZZI, SERENA
A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibβ in the pathophysiology of bernard‐soulier syndrome and gpib‐ix complex assembly
2021-01-01 Barozzi, S.; Bozzi, V.; De Rocco, D.; Giangregorio, T.; Noris, P.; Savoia, A.; Pecci, A.
Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia
2016-01-01 Melazzini, Federica; Palombo, Flavia; Balduini, Alessandra; De Rocco, Daniela; Marconi, Caterina; Noris, Patrizia; Gnan, Chiara; Pippucci, Tommaso; Bozzi, Valeria; Faleschini, Michela; Barozzi, Serena; Doubek, Michael; Di Buduo, Christian A.; Kozubik, Katerina Stano; Radova, Lenka; Loffredo, Giuseppe; Pospisilova, Sarka; Alfano, Caterina; Seri, Marco; Balduini, Carlo L.; Pecci, Alessandro; Savoia, Anna
Eltrombopag for the treatment of inherited thrombocytopenias: A phase II clinical trial
2020-01-01 Zaninetti, C.; Gresele, P.; Bertomoro, A.; Klersy, C.; de Candia, E.; Veneri, D.; Barozzi, S.; Fierro, T.; Alberelli, M. A.; Musella, V.; Noris, P.; Fabris, F.; Balduini, C. L.; Pecci, A.
Eltrombopag in preparation for surgery in patients with severe MYH9-related thrombocytopenia
2019-01-01 Zaninetti, C.; Barozzi, S.; Bozzi, V.; Gresele, P.; Balduini, C. L.; Pecci, A.
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup
2023-01-01 Marconi, Caterina; Pecci, Alessandro; Palombo, Flavia; Melazzini, Federica; Bottega, Roberta; Nardi, Elena; Bozzi, Valeria; Faleschini, Michela; Barozzi, Serena; Giangregorio, Tania; Magini, Pamela; Balduini, Carlo L; Savoia, Anna; Seri, Marco; Noris, Patrizia; Pippucci, Tommaso
Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
2017-01-01 Zaninetti, C.; Santini, V.; Tiniakou, M.; Barozzi, S.; Savoia, A.; Pecci, A.
Miniaturized 3d bone marrow tissue model to assess response to thrombopoietin-receptor agonists in patients
2021-01-01 Di Buduo, C. A.; Laurent, P. -A.; Zaninetti, C.; Lordier, L.; Soprano, P. M.; Ntai, A.; Barozzi, S.; La Spada, A.; Biunno, I.; Raslova, H.; Bussel, J. B.; Kaplan, D. L.; Balduini, C. L.; Pecci, A.; Balduini, A.
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim
2018-01-01 Pecci, Alessandro; Ragab, Iman; Bozzi, Valeria; De Rocco, Daniela; Barozzi, Serena; Giangregorio, Tania; Ali, Heba; Melazzini, Federica; Sallam, Mohamed; Alfano, Caterina; Pastore, Annalisa; Balduini, Carlo L; Savoia, Anna
Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombocytopenia
2013-01-01 Necchi, Vittorio; Balduini, Alessandra; Noris, Patrizia; Barozzi, Serena; Sommi, Patrizia; di Buduo, Christian; Balduini, Carlo L.; Solcia, Enrico; Pecci, Alessandro
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel mutation in gp1bb reveals the role of the cytoplasmic domain of gpibβ in the pathophysiology of bernard‐soulier syndrome and gpib‐ix complex assembly | 1-gen-2021 | Barozzi, S.; Bozzi, V.; De Rocco, D.; Giangregorio, T.; Noris, P.; Savoia, A.; Pecci, A. | |
| Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia | 1-gen-2016 | Melazzini, Federica; Palombo, Flavia; Balduini, Alessandra; De Rocco, Daniela; Marconi, Caterina; Noris, Patrizia; Gnan, Chiara; Pippucci, Tommaso; Bozzi, Valeria; Faleschini, Michela; Barozzi, Serena; Doubek, Michael; Di Buduo, Christian A.; Kozubik, Katerina Stano; Radova, Lenka; Loffredo, Giuseppe; Pospisilova, Sarka; Alfano, Caterina; Seri, Marco; Balduini, Carlo L.; Pecci, Alessandro; Savoia, Anna | |
| Eltrombopag for the treatment of inherited thrombocytopenias: A phase II clinical trial | 1-gen-2020 | Zaninetti, C.; Gresele, P.; Bertomoro, A.; Klersy, C.; de Candia, E.; Veneri, D.; Barozzi, S.; Fierro, T.; Alberelli, M. A.; Musella, V.; Noris, P.; Fabris, F.; Balduini, C. L.; Pecci, A. | |
| Eltrombopag in preparation for surgery in patients with severe MYH9-related thrombocytopenia | 1-gen-2019 | Zaninetti, C.; Barozzi, S.; Bozzi, V.; Gresele, P.; Balduini, C. L.; Pecci, A. | |
| Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup | 1-gen-2023 | Marconi, Caterina; Pecci, Alessandro; Palombo, Flavia; Melazzini, Federica; Bottega, Roberta; Nardi, Elena; Bozzi, Valeria; Faleschini, Michela; Barozzi, Serena; Giangregorio, Tania; Magini, Pamela; Balduini, Carlo L; Savoia, Anna; Seri, Marco; Noris, Patrizia; Pippucci, Tommaso | |
| Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases | 1-gen-2017 | Zaninetti, C.; Santini, V.; Tiniakou, M.; Barozzi, S.; Savoia, A.; Pecci, A. | |
| Miniaturized 3d bone marrow tissue model to assess response to thrombopoietin-receptor agonists in patients | 1-gen-2021 | Di Buduo, C. A.; Laurent, P. -A.; Zaninetti, C.; Lordier, L.; Soprano, P. M.; Ntai, A.; Barozzi, S.; La Spada, A.; Biunno, I.; Raslova, H.; Bussel, J. B.; Kaplan, D. L.; Balduini, C. L.; Pecci, A.; Balduini, A. | |
| Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim | 1-gen-2018 | Pecci, Alessandro; Ragab, Iman; Bozzi, Valeria; De Rocco, Daniela; Barozzi, Serena; Giangregorio, Tania; Ali, Heba; Melazzini, Federica; Sallam, Mohamed; Alfano, Caterina; Pastore, Annalisa; Balduini, Carlo L; Savoia, Anna | |
| Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombocytopenia | 1-gen-2013 | Necchi, Vittorio; Balduini, Alessandra; Noris, Patrizia; Barozzi, Serena; Sommi, Patrizia; di Buduo, Christian; Balduini, Carlo L.; Solcia, Enrico; Pecci, Alessandro |