List of works - Federica Melazzini

5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia

scientific article published on 18 January 2017

A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.

scientific article published on 3 May 2017

ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia

scientific article published on 23 October 2018

Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders

scientific article published on 21 April 2015

Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias

scientific article

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

scientific article published on 6 April 2017

Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

scientific article

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)

scientific article

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia

scientific article

Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy

scientific article published on 05 January 2021

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations

scientific article

Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias?

scientific article published on 16 September 2017

Inherited thrombocytopenias-recent advances in clinical and molecular aspects

scientific article

Letter

scientific article published on 01 June 2016

Massive mediastinal enlargement due to extramedullary haematopoiesis in a patient with MYH9-related thrombocytopenia.

scientific article

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.

scientific article

Mutations of RUNX1 in families with inherited thrombocytopenia.

scientific article

New roles for mean platelet volume measurement in the clinical practice?

scientific article

Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia.

scientific article published on 8 May 2015

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

scientific article

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia.

scientific article

Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study

scientific article

Research at the heart of hematology: thrombocytopenias and platelet function disorders

scientific article published on February 2017

Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim

scientific article

Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy

scientific article published on 08 November 2020

List of works by Federica Melazzini

5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia

A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.

ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia

Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders

Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)

Clinical and pathogenic features of ETV6-related thrombocytopenia with predisposition to acute lymphoblastic leukemia

Correction to: Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy

Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations

Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias?

Inherited thrombocytopenias-recent advances in clinical and molecular aspects

Letter

Massive mediastinal enlargement due to extramedullary haematopoiesis in a patient with MYH9-related thrombocytopenia.

Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.

Mutations of RUNX1 in families with inherited thrombocytopenia.

New roles for mean platelet volume measurement in the clinical practice?

Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia.

Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia.

Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study

Research at the heart of hematology: thrombocytopenias and platelet function disorders

Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim

Venous thromboembolism and COVID-19: a single center experience from an academic tertiary referral hospital of Northern Italy