Mimosa Mortarino

Milan, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 9 publications

Preimplantation Genetic Testing for Families at Risk of Haemophilia: Ten-Year Single-Centre Experience.

Preimplantation Genetic Testing for Families at Risk of Haemophilia: Ten-Year Single-Centre Experience.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: January 27, 2026

Gender equity in hemophilia: need for healthcare, familial, and societal advocacy.

Gender equity in hemophilia: need for healthcare, familial, and societal advocacy.

Journal: Frontiers in medicine

Published: November 27, 2023

Knowledge and attitudes toward gene therapy of a cohort of Italian patients with hemophilia.

Knowledge and attitudes toward gene therapy of a cohort of Italian patients with hemophilia.

Journal: Journal of thrombosis and haemostasis : JTH

Published: August 09, 2023

Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor.

Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor.

Journal: International journal of molecular sciences

Published: June 28, 2023

Psychological and cognitive factors involved in decision-making process of haemophilia carriers in reproductive choices.

Psychological and cognitive factors involved in decision-making process of haemophilia carriers in reproductive choices.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: April 16, 2023

X Chromosome inactivation: a modifier of factor VIII and IX plasma levels and bleeding phenotype in Haemophilia carriers.

X Chromosome inactivation: a modifier of factor VIII and IX plasma levels and bleeding phenotype in Haemophilia carriers.

Journal: European journal of human genetics : EJHG

Published: January 14, 2020

Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity.

Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity.

Journal: Haematologica

Published: August 10, 2017

A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect.

A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients: evidence for a founder effect.

Journal: Molecular genetics & genomic medicine

Published: April 27, 2015

Reproductive care in human immunodeficiency virus serodiscordant couples with haemophilia.

Reproductive care in human immunodeficiency virus serodiscordant couples with haemophilia.

Journal: Blood transfusion = Trasfusione del sangue

Published: April 20, 2012

Showing 1-9 of 9

Last Updated: 09/26/2026