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.
ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype
2024-01-01 Eva Zanchetta, Melania; Barozzi, Serena; Isidori, Federica; Marconi, Caterina; Farinasso, Loredana; Bottega, Roberta; Savoia, Anna; Pecci, Alessandro; Faleschini, Michela
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.
Isolated thrombocytopenia in pregnancy: A monocentric retrospective study of 63 pregnancies in 59 women
2024-01-01 Freddi, Giulia; Parimbelli, Enea; Vai, Federico; Quaglini, Silvana; Bozzi, Valeria; Barozzi, Serena; Beneventi, Fausta; DE MAGGIO, Irene; Cavagnoli, Chiara; DI SABATINO, Antonio; Noris, Patrizia; Melazzini, Federica
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.
Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC
2021-01-01 Barozzi, S.; Di Buduo, C. A.; Marconi, C.; Bozzi, V.; Seri, M.; Romano, F.; Balduini, A.; Pecci, A.
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene
2024-01-01 Marzollo, Antonio; Zampieri, Stefania; Barozzi, Serena; Abrar Yousaf, Muhammad; Quartararo, Jade; De Rocco, Daniela; Faleschini, Michela; Marconi, Caterina; Ceccatelli Berti, Camilla; Bozzi, Valeria; Russo, Giovanna; Giordano, Paola; Goffrini, Paola; Bresolin, Silvia; Pastore, Annalisa; Savoia, Anna; Pecci, Alessandro
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
Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis
2024-01-01 Kamiya, Laureano J.; Barozzi, Serena; Isidori, Federica; Ganiewich, Daiana; De Luca, Geraldine; Bozzi, Valeria; Marta, Rosana F.; Melazzini, Federica; Pippucci, Tommaso; Heller, Paula G.; Glembotsky, Ana C.; Pecci, Alessandro
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. | |
| ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype | 1-gen-2024 | Eva Zanchetta, Melania; Barozzi, Serena; Isidori, Federica; Marconi, Caterina; Farinasso, Loredana; Bottega, Roberta; Savoia, Anna; Pecci, Alessandro; Faleschini, Michela | |
| 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. | |
| Isolated thrombocytopenia in pregnancy: A monocentric retrospective study of 63 pregnancies in 59 women | 1-gen-2024 | Freddi, Giulia; Parimbelli, Enea; Vai, Federico; Quaglini, Silvana; Bozzi, Valeria; Barozzi, Serena; Beneventi, Fausta; DE MAGGIO, Irene; Cavagnoli, Chiara; DI SABATINO, Antonio; Noris, Patrizia; Melazzini, Federica | |
| 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. | |
| Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC | 1-gen-2021 | Barozzi, S.; Di Buduo, C. A.; Marconi, C.; Bozzi, V.; Seri, M.; Romano, F.; Balduini, A.; Pecci, A. | |
| Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene | 1-gen-2024 | Marzollo, Antonio; Zampieri, Stefania; Barozzi, Serena; Abrar Yousaf, Muhammad; Quartararo, Jade; De Rocco, Daniela; Faleschini, Michela; Marconi, Caterina; Ceccatelli Berti, Camilla; Bozzi, Valeria; Russo, Giovanna; Giordano, Paola; Goffrini, Paola; Bresolin, Silvia; Pastore, Annalisa; Savoia, Anna; Pecci, Alessandro | |
| 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 | |
| Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis | 1-gen-2024 | Kamiya, Laureano J.; Barozzi, Serena; Isidori, Federica; Ganiewich, Daiana; De Luca, Geraldine; Bozzi, Valeria; Marta, Rosana F.; Melazzini, Federica; Pippucci, Tommaso; Heller, Paula G.; Glembotsky, Ana C.; Pecci, Alessandro | |
| 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 |