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 ERYTHROCYTOSIS ARE RARE DISORDERS WITH MANY GENES INVOLVED. FUNCTIONAL EVALUATION OF NOVEL PHD2 AND EPOR MUTATIONS.
2016 Peroni, Edoardo
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