Samin Mohsenian
Milan, Italy
Last Updated: 09/26/2026
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Found 10 publications
The thrombotic paradox in congenital fibrinogen deficiencies: from pathophysiology to practice.
Journal: Research and practice in thrombosis and haemostasis
Published: May 03, 2025
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
Rare inherited coagulation disorders: no longer orphan and neglected.
Journal: Research and practice in thrombosis and haemostasis
Published: March 20, 2024
Exploring nonreplacement therapies' impact on hemophilia and other rare bleeding disorders.
Journal: Research and practice in thrombosis and haemostasis
Published: January 10, 2024
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Journal: Blood advances
Published: November 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
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.
Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis
Published: April 04, 2021
Rare inherited coagulation disorders and thrombosis.
Journal: Haematologica
Published: September 10, 2020
Showing 1-10 of 10
Last Updated: 09/26/2026