Marzia Menegatti
Milan, Italy
Last Updated: 09/26/2026
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Found 45 publications
Gynecologic and obstetric complications in women with congenital fibrinogen disorders: insights from the Prospective Rare Bleeding Disorders Database.
Journal: Research and practice in thrombosis and haemostasis
Published: March 18, 2025
The genetic spectrum of rare bleeding disorders.
Journal: Journal of thrombosis and haemostasis : JTH
Published: February 21, 2025
Clinical, Laboratory Aspects and Management of Factor X Deficiency.
Journal: Seminars in thrombosis and hemostasis
Published: August 29, 2024
Rare inherited coagulation disorders: no longer orphan and neglected.
Journal: Research and practice in thrombosis and haemostasis
Published: March 20, 2024
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Journal: Blood advances
Published: November 15, 2023
Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for ultra-rare inherited bleeding disorders.
Journal: Expert review of hematology
Published: March 15, 2023
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficiencies.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: December 16, 2022
Safety and effectiveness of recombinant factor XIII-A2 in congenital factor XIII deficiency: Real-world evidence.
Journal: Research and practice in thrombosis and haemostasis
Published: May 25, 2021
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family.
Journal: Haematologica
Published: April 09, 2021
Management of rare acquired bleeding disorders.
Journal: Hematology. American Society of Hematology. Education Program
Published: December 07, 2019
Last Updated: 09/26/2026