Daniela De Rocco

Trieste, Italy

Last Updated: 09/26/2026

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Found 29 publications

Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene.

Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene.

Journal: British journal of haematology

Published: January 19, 2024

A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly.

A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly.

Journal: International journal of molecular sciences

Published: August 19, 2021

Renin Angiotensin System, COVID-19 and Male Fertility: Any Risk for Conceiving?

Renin Angiotensin System, COVID-19 and Male Fertility: Any Risk for Conceiving?

Journal: Microorganisms

Published: August 06, 2020

MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.

MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.

Journal: Hamostaseologie

Published: July 12, 2018

Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim.

Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim.

Journal: EMBO molecular medicine

Published: December 02, 2017

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.

Journal: Haematologica

Published: July 12, 2017

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

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

Journal: British journal of haematology

Published: May 04, 2017

MYH9 gene mutations associated with bleeding.

MYH9 gene mutations associated with bleeding.

Journal: Platelets

Published: April 04, 2017

Mutations of RUNX1 in families with inherited thrombocytopenia.

Mutations of RUNX1 in families with inherited thrombocytopenia.

Journal: American journal of hematology

Published: February 20, 2017

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

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

Journal: Haematologica

Published: April 06, 2016

Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian Association of Pediatric Hematology-Oncology).

Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian Association of Pediatric Hematology-Oncology).

Journal: American journal of hematology

Published: March 04, 2016

Molecular diagnosis of thrombocytopenia-absent radius syndrome using next-generation sequencing.

Molecular diagnosis of thrombocytopenia-absent radius syndrome using next-generation sequencing.

Journal: International journal of laboratory hematology

Published: February 01, 2016

Showing 1-12 of 29

Last Updated: 09/26/2026