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Edoardo Peroni

Showing results (11-20 of 18) with videos related to

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International Journal of Molecular Sciences|December 11, 2025
Methodological Assessment of High-Throughput Sequencing Platforms: Illumina vs. MGI in Clinical-Grade <i>CFTR</i> GenotypingMarianna Beggio, Edoardo Peroni, Eliana Greco, et al.
European Journal of Haematology|April 30, 2013
Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiencyAntonio Girolami, Giulia Berti de Marinis, Irene Bertozzi, et al.
European Journal of Clinical Investigation|June 9, 2016
Thrombotic risk correlates with mutational status in true essential thrombocythemiaIrene Bertozzi, Edoardo Peroni, Giacomo Coltro, et al.
Seminars in Thrombosis and Hemostasis|July 31, 2014
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 5Antonio Girolami, Josè Vidal, Marcela Sabagh, et al.
Clinical Chemistry and Laboratory Medicine|September 16, 2018
Preanalytical stability of [-2]proPSA in whole blood stored at room temperature before separation of serum and plasma: implications to Phi determinationRuggero Dittadi, Aline S C Fabricio, Giulia Rainato, et al.
Cancers|January 21, 2022
High ETV6 Levels Support Aggressive B Lymphoma Cell Survival and Predict Poor Outcome in Diffuse Large B-Cell Lymphoma PatientsDario Marino, Marco Pizzi, Iuliia Kotova, et al.
British Journal of Haematology|February 27, 2015
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohortMaria L Randi, Giulia Geranio, Irene Bertozzi, et al.
Haematologica|June 15, 2023
Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosisMarine Delamare, Amandine Le Roy, Mathilde Pacault, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
International Journal of Molecular Sciences|December 11, 2025
Methodological Assessment of High-Throughput Sequencing Platforms: Illumina vs. MGI in Clinical-Grade <i>CFTR</i> GenotypingMarianna Beggio, Edoardo Peroni, Eliana Greco, et al.
European Journal of Haematology|April 30, 2013
Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiencyAntonio Girolami, Giulia Berti de Marinis, Irene Bertozzi, et al.
European Journal of Clinical Investigation|June 9, 2016
Thrombotic risk correlates with mutational status in true essential thrombocythemiaIrene Bertozzi, Edoardo Peroni, Giacomo Coltro, et al.
Seminars in Thrombosis and Hemostasis|July 31, 2014
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 5Antonio Girolami, Josè Vidal, Marcela Sabagh, et al.
Clinical Chemistry and Laboratory Medicine|September 16, 2018
Preanalytical stability of [-2]proPSA in whole blood stored at room temperature before separation of serum and plasma: implications to Phi determinationRuggero Dittadi, Aline S C Fabricio, Giulia Rainato, et al.
Cancers|January 21, 2022
High ETV6 Levels Support Aggressive B Lymphoma Cell Survival and Predict Poor Outcome in Diffuse Large B-Cell Lymphoma PatientsDario Marino, Marco Pizzi, Iuliia Kotova, et al.
British Journal of Haematology|February 27, 2015
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohortMaria L Randi, Giulia Geranio, Irene Bertozzi, et al.
Haematologica|June 15, 2023
Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosisMarine Delamare, Amandine Le Roy, Mathilde Pacault, et al.
Pageof 2