PERONI, EDOARDO

PERONI, EDOARDO  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Effect of busulfan on JAK2V617F allele burden. 2014 RANDI, MARIA LUIGIASANTAROSSA, CLAUDIAPERONI, EDOARDOCOSI, ELISABETTADUNER, ELENABERTOZZI, IRENEFABRIS, FABRIZIO HAEMATOLOGICA - -
Associated risk factors and arterial occlusions in patients with von Willebrand disease: Analysis of the literature and report of two cases 2014 GIROLAMI, ANTONIOFERRARI, SILVIABERTOMORO, ANTONELLAPERONI, EDOARDOSAMBADO, LUISACASONATO, SANDRA CASE REPORTS IN INTERNAL MEDICINE - -
Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders: A Critical Analysis of All Reported Cases. 2014 GIROLAMI, ANTONIOFERRARI, SILVIASAMBADO, LUISAPERONI, EDOARDOCOSI, ELISABETTA CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS - -
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort 2015 RANDI, MARIA LUIGIAIrene BertozziPERONI, EDOARDOBASSO, GIUSEPPEFABRIS, FABRIZIO + BRITISH JOURNAL OF HAEMATOLOGY - -
Congenital FXI and FVII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: an intriguing observation. 2015 Girolami, A.Peroni, E.Ferrari, S.Lombardi, A. M + HEMATOLOGY - -
Impact of mutational status on pregnancy outcome in patients with essential thrombocytemia 2015 BERTOZZI, IRENEPERONI, EDOARDORANDI, MARIA LUIGIA + HAEMATOLOGICA - -
Mutational profile of childhood myeloproliferative neoplasms 2015 PERONI, EDOARDORANDI, MARIA LUIGIA + LEUKEMIA - -
Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature. 2015 GIROLAMI, ANTONIOSAMBADO, LUISAPERONI, EDOARDOCASONATO, SANDRA + BLOOD COAGULATION & FIBRINOLYSIS - -
Thrombotic risk correlates with mutational status in true-essential thrombocythemia 2016 BERTOZZI, IRENEPERONI, EDOARDOBOGONI, GIULIACOSI, ELISABETTASANTAROSSA, CLAUDIAFABRIS, FABRIZIORANDI, MARIA LUIGIA + EUROPEAN JOURNAL OF CLINICAL INVESTIGATION - -
Pulmonary embolism in congenital bleeding disorders: Intriguing discrepancies among different clotting factors deficiencies 2016 Girolami A.Cosi E.Tasinato V.Peroni E. + BLOOD COAGULATION & FIBRINOLYSIS - -
Ischemic strokes in congenital bleeding disorders: comparison with myocardial infarction and other acute coronary syndromes 2016 GIROLAMI, ANTONIOFERRARI, SILVIACOSI, ELISABETTAPERONI, EDOARDOFABRIS, FABRIZIO Cardiovascular & Hematological Disorders-Drug Targets - -
Two novel missense mutations in EPOR gene causes erythrocytosis in two unrelated patients 2016 Peroni, EdoardoBertozzi, IreneBiagetti, GiacomoFabris, FabrizioMaria Luigia Randi + BRITISH JOURNAL OF HAEMATOLOGY - -
Idiopathic erythrocytosis: a study of a large cohort with a long follow-up 2016 RANDI, MARIA LUIGIABERTOZZI, IRENECOSI, ELISABETTASANTAROSSA, CLAUDIAPERONI, EDOARDOFABRIS, FABRIZIO ANNALS OF HEMATOLOGY - -
CONGENITAL ERYTHROCYTOSIS ARE RARE DISORDERS WITH MANY GENES INVOLVED. FUNCTIONAL EVALUATION OF NOVEL PHD2 AND EPOR MUTATIONS. 2016 Peroni, Edoardo - - -
Bone marrow histology for the diagnosis of essential thrombocythemia in children: a multi-center Italian study 2017 PIZZI, MARCOBERTOZZI, IRENERAMENGHI, UGOPERONI, EDOARDORUGGE, MASSIMOFABRIS, FABRIZIORANDI, MARIA LUIGIA + BLOOD - -
Antibodies to post-translationally modified mitochondrial peptide PDC-E2(167–184) in type 1 diabetes 2018 Peroni E.Traldi P.Lapolla A. + ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS - -
High ETV6 Levels Support Aggressive B Lymphoma Cell Survival and Predict Poor Outcome in Diffuse Large B-Cell Lymphoma Patients 2022 Pizzi, MarcoGuzzardo, VincenzaTalli, IlariaPeroni, EdoardoScapinello, GretaDei Tos, Angelo PaoloPiazza, FrancescoTrentin, LivioZagonel, VittorinaPiovan, Erich + CANCERS - -