Federica Melazzini

7PUBLICATIONS
13CO-AUTHORS
HaematologyGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Cardiovascular medicine and haematology not elsewhere classified
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Publications (7)

|Oct 08, 2024
Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis.

Laureano J Kamiya, Serena Barozzi, Federica Isidori

|Jan 05, 2021
Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy.

Federica Melazzini, Marta Colaneri, Federica Fumoso

|Nov 08, 2020
Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy.

Federica Melazzini, Marta Colaneri, Federica Fumoso

|Oct 24, 2018
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia.

Michela Faleschini, Federica Melazzini, Caterina Marconi

|Jun 09, 2017
Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias.

F Melazzini, C Zaninetti, C L Balduini

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