PERONI, EDOARDO
PERONI, EDOARDO
Acute myeloid leukemia: from NGS, through scRNA-seq, to CAR-T. dissect cancer heterogeneity and tailor the treatment
2023 Peroni, Edoardo; Randi, Maria Luigia; Rosato, Antonio; Cagnin, Stefano
Antibodies to post-translationally modified mitochondrial peptide PDC-E2(167–184) in type 1 diabetes
2018 Nuti, F.; Gallo, A.; Real-Fernandez, F.; Crulli, M.; Rentier, C.; Piarulli, F.; Peroni, E.; Rossi, G.; Traldi, P.; Rovero, P.; Lapolla, A.; Papini, A. M.
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort
2015 Randi, MARIA LUIGIA; Giulia, Geranio; Bertozzi, Irene; Concetta, Micalizzi; Ugo, Ramenghi; Fabio, Tucci; Notarangelo, Lucia D.; Saverio, Ladogana; Giuseppe, Menna; Paola, Giordano; Caterina, Consarino; Piero, Farruggia; Zanazzo, Giulio A.; Fiori, Giovanni M.; Roberta, Burnelli; Giovanna, Russo; Momcilo, Jankovich; Peroni, Edoardo; Elena, Duner; Basso, Giuseppe; Fabris, Fabrizio; Putti, Maria C.
Associated risk factors and arterial occlusions in patients with von Willebrand disease: Analysis of the literature and report of two cases
2014 Girolami, Antonio; Ferrari, Silvia; Bertomoro, Antonella; Peroni, Edoardo; Sambado, Luisa; Casonato, Sandra
Bone marrow histology for the diagnosis of essential thrombocythemia in children: a multi-center Italian study
2017 Putti, Maria Caterina; Pizzi, Marco; Bertozzi, Irene; Sabattini, Elena; Micalizzi, Concetta; Farruggia, Piero; Ramenghi, Ugo; Cesaro, Simone; Russo, Giovanna; Peroni, Edoardo; Rugge, Massimo; Fabris, Fabrizio; Randi, MARIA LUIGIA
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis
2023 Delamare, Marine; Le Roy, Amandine; Pacault, Mathilde; Schmitt, Loïc; Garrec, Céline; Maaziz, Nada; Myllykoski, Matti; Rimbert, Antoine; Karaghiannis, Valéna; Aral, Bernard; Catherwood, Mark; Airaud, Fabrice; Mansour-Hendili, Lamisse; Hoogewijs, David; Peroni, Edoardo; Idriss, Salam; Lesieur, Valentine; Caillaud, Amandine; Si-Tayeb, Karim; Chariau, Caroline; Gaignerie, Anne; Rab, Minke; Haferlach, Torsten; Meggendorfer, Manja; Bézieau, Stéphane; Benetti, Andrea; Casadevall, Nicole; Hirsch, Pierre; Rose, Christian; Wemeau, Mathieu; Galacteros, Frédéric; Cassinat, Bruno; Bellosillo, Beatriz; Bento, Celeste; Van Wijk, Richard; Petrides, Petro E; Randi, Maria Luigia; Mcmullin, Mary Frances; Koivunen, Peppi; Girodon, François; Gardie, Betty
Congenital FXI and FVII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: an intriguing observation.
2015 Girolami, A.; Peroni, E.; Girolami, B.; Ferrari, S.; Lombardi, A. M
Effect of busulfan on JAK2V617F allele burden.
2014 Randi, MARIA LUIGIA; Santarossa, Claudia; Peroni, Edoardo; Cosi, Elisabetta; Duner, Elena; Bertozzi, Irene; Fabris, Fabrizio
Hematologic Neoplasms Associated with Down Syndrome: Cellular and Molecular Heterogeneity of the Diseases
2023 Peroni, Edoardo; Gottardi, Michele; D'Antona, Lucia; Randi, Maria Luigia; Rosato, Antonio; Coltro, Giacomo
High ETV6 Levels Support Aggressive B Lymphoma Cell Survival and Predict Poor Outcome in Diffuse Large B-Cell Lymphoma Patients
2022 Marino, Dario; Pizzi, Marco; Kotova, Iuliia; Schmidt, Ronny; Schröder, Christoph; Guzzardo, Vincenza; Talli, Ilaria; Peroni, Edoardo; Finotto, Silvia; Scapinello, Greta; Dei Tos, Angelo Paolo; Piazza, Francesco; Trentin, Livio; Zagonel, Vittorina; Piovan, Erich
Idiopathic erythrocytosis: a study of a large cohort with a long follow-up
2016 Randi, MARIA LUIGIA; Bertozzi, Irene; Cosi, Elisabetta; Santarossa, Claudia; Peroni, Edoardo; Fabris, Fabrizio
Impact of mutational status on pregnancy outcome in patients with essential thrombocytemia
2015 Rumi, Elisa; Bertozzi, Irene; Casetti, Ilaria C.; Roncoroni, Elisa; Cavalloni, Chiara; Bellini, Marta; Sant’Antonio, Emanuela; Gotti, Manuel; Ferretti, Virginia V.; Milanesi, Chiara; Peroni, Edoardo; Pietra, Daniela; Astori, Cesare; Randi, MARIA LUIGIA; Cazzola, Mario
Ischemic strokes in congenital bleeding disorders: comparison with myocardial infarction and other acute coronary syndromes
2016 Girolami, Antonio; Ferrari, Silvia; Cosi, Elisabetta; Peroni, Edoardo; Fabris, Fabrizio
Mutational profile of childhood myeloproliferative neoplasms
2015 Karow, A; Nienhold, R.; Lundberg, P.; Peroni, Edoardo; Putti, M. C.; Randi, MARIA LUIGIA; Skoda, R. C.
Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders: A Critical Analysis of All Reported Cases.
2014 Girolami, Antonio; Ferrari, Silvia; Sambado, Luisa; Peroni, Edoardo; Cosi, Elisabetta
Pulmonary embolism in congenital bleeding disorders: Intriguing discrepancies among different clotting factors deficiencies
2016 Girolami, A.; Cosi, E.; Tasinato, V.; Peroni, E.; Girolami, B.; Lombardi, A. M.
Thrombotic risk correlates with mutational status in true-essential thrombocythemia
2016 Bertozzi, Irene; Peroni, Edoardo; Coltro, G; Bogoni, Giulia; Cosi, Elisabetta; Santarossa, Claudia; Fabris, Fabrizio; Randi, MARIA LUIGIA
Two novel missense mutations in EPOR gene causes erythrocytosis in two unrelated patients
2016 Peroni, Edoardo; Bertozzi, Irene; Gherlinzoni, Filippo; Stefani, Piero M.; Lombardi, Annamaria; Biagetti, Giacomo; Fabris, Fabrizio; Randi, MARIA LUIGIA
Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature.
2015 Girolami, Antonio; Tasinato, V; Sambado, Luisa; Peroni, Edoardo; Casonato, Sandra