Publications by authors named "Edoardo Peroni"

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Methodological Assessment of High-Throughput Sequencing Platforms: Illumina vs. MGI in Clinical-Grade Genotyping.
Marianna Beggio, Edoardo Peroni, Eliana Greco, Giulia Favretto, Dario Degiorgio

Int J Mol Sci· December 2025

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Spatial-transcriptomic profiling: a new lens for understanding myelofibrosis pathophysiology.
Edoardo Peroni, Elisabetta Calistri, Rosario Amato, Michele Gottardi, Antonio Rosato

Cell Commun Signal· October 2024

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Characterization of genetic variants in the gene identified in a European collection of patients with erythrocytosis.
Marine Delamare, Amandine Le Roy, Mathilde Pacault, Loïc Schmitt, Céline Garrec, Edoardo Peroni

Haematologica· November 2023

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Acute myeloid leukemia: from NGS, through scRNA-seq, to CAR-T. dissect cancer heterogeneity and tailor the treatment.
Edoardo Peroni, Maria Luigia Randi, Antonio Rosato, Stefano Cagnin

J Exp Clin Cancer Res· October 2023

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Hematologic Neoplasms Associated with Down Syndrome: Cellular and Molecular Heterogeneity of the Diseases.
Edoardo Peroni, Michele Gottardi, Lucia D'Antona, Maria Luigia Randi, Antonio Rosato

Int J Mol Sci· October 2023

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Emission estimates and air quality simulation on Lombardy during lockdown.
Alessandro Marongiu, Elisabetta Angelino, Giulia Malvestiti, Marco Moretti, Giuseppe Fossati, Edoardo Peroni

Air Qual Atmos Health· October 2022

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High ETV6 Levels Support Aggressive B Lymphoma Cell Survival and Predict Poor Outcome in Diffuse Large B-Cell Lymphoma Patients.
Dario Marino, Marco Pizzi, Iuliia Kotova, Ronny Schmidt, Christoph Schröder, Edoardo Peroni

Cancers (Basel)· January 2022

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Insights on Metabolic Reprogramming and Its Therapeutic Potential in Acute Leukemia.
Ludovica Di Martino, Valeria Tosello, Edoardo Peroni, Erich Piovan

Int J Mol Sci· August 2021

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Preanalytical stability of [-2]proPSA in whole blood stored at room temperature before separation of serum and plasma: implications to Phi determination.
Ruggero Dittadi, Aline S C Fabricio, Giulia Rainato, Edoardo Peroni, Fulvio Di Tonno

Clin Chem Lab Med· March 2019

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Two novel missense mutations in EPOR gene causes erythrocytosis in two unrelated patients.
Edoardo Peroni, Irene Bertozzi, Filippo Gherlinzoni, Piero M Stefani, AnnaMaria Lombardi

Br J Haematol· March 2018

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Bone marrow histology for the diagnosis of essential thrombocythemia in children: a multicenter Italian study.
Maria Caterina Putti, Marco Pizzi, Irene Bertozzi, Elena Sabattini, Concetta Micalizzi, Edoardo Peroni

Blood· June 2017

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Ischemic Strokes in Congenital Bleeding Disorders: Comparison with Myocardial Infarction and other Acute Coronary Syndromes.
Antonio Girolami, Ferrari Silvia, Cosi Elisabetta, Peroni Edoardo, Girolami Bruno

Cardiovasc Hematol Disord Drug Targets· February 2017

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Thrombotic risk correlates with mutational status in true essential thrombocythemia.
Irene Bertozzi, Edoardo Peroni, Giacomo Coltro, Giulia Bogoni, Elisabetta Cosi

Eur J Clin Invest· August 2016

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Pulmonary embolism in congenital bleeding disorders: intriguing discrepancies among different clotting factors deficiencies.
Antonio Girolami, Elisabetta Cosi, Valentina Tasinato, Edoardo Peroni, Bruno Girolami

Blood Coagul Fibrinolysis· July 2016

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Idiopathic erythrocytosis: a study of a large cohort with a long follow-up.
Maria Luigia Randi, Irene Bertozzi, Elisabetta Cosi, Claudia Santarossa, Edoardo Peroni

Ann Hematol· January 2016

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Impact of mutational status on pregnancy outcome in patients with essential thrombocytemia.
Elisa Rumi, Irene Bertozzi, Ilaria C Casetti, Elisa Roncoroni, Chiara Cavalloni, Edoardo Peroni

Haematologica· November 2015

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Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported cases.
Antonio Girolami, Silvia Ferrari, Luisa Sambado, Edoardo Peroni, Elisabetta Cosi

Clin Appl Thromb Hemost· May 2015

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Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort.
Maria L Randi, Giulia Geranio, Irene Bertozzi, Concetta Micalizzi, Ugo Ramenghi, Edoardo Peroni

Br J Haematol· May 2015

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Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature.
Antonio Girolami, Valentina Tasinato, Luisa Sambado, Edoardo Peroni, Allesandra Casonato

Blood Coagul Fibrinolysis· January 2015

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The old and the new in prekallikrein deficiency: historical context and a family from Argentina with PK deficiency due to a new mutation (Arg541Gln) in exon 14 associated with a common polymorphysm (Asn124Ser) in exon 5.
Antonio Girolami, Josè Vidal, Marcela Sabagh, Nora Gervan, Maria Parody, Edoardo Peroni

Semin Thromb Hemost· July 2014

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A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15.
Antonio Girolami, Luisa Sambado, Edoardo Peroni, Liliana Santarossa, Anna M Lombardi

Blood Coagul Fibrinolysis· March 2014

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Effect of busulfan on JAK2V617F allele burden.
Maria Luigia Randi, Claudia Santarossa, Edoardo Peroni, Elisabetta Cosi, Elena Duner

Haematologica· March 2014

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Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiency.
Antonio Girolami, Giulia Berti de Marinis, Irene Bertozzi, Edoardo Peroni, Valentina Tasinato

Eur J Haematol· August 2013

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