Giovanna Cozzi
Milan, Italy
Last Updated: 09/26/2026
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Found 15 publications
Evaluation of different platelet-dependent von Willebrand factor activity assays to assess the in vivo inhibitory effect of caplacizumab on the von Willebrand factor-platelet interaction.
Journal: Journal of thrombosis and haemostasis : JTH
Published: March 06, 2025
Effect of the Polymorphic Variant p.D1472H on the Platelet-Dependent VWF Activity Assays.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: February 18, 2025
Variant p.Tyr1584Cys: a frequent von Willebrand factor variant in search of von Willebrand disease.
Journal: Research and practice in thrombosis and haemostasis
Published: May 10, 2024
Type 2M/2A von Willebrand disease: a shared phenotype between type 2M and 2A.
Journal: Blood advances
Published: January 10, 2024
Clinical and Laboratory Presentation and Underlying Mechanism in Patients with Low VWF.
Journal: Thrombosis and haemostasis
Published: October 06, 2023
Erratum to 'A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays.' [Research and Practice in Thrombosis and Haemostasis Volume 7, Issue 3, March 2023, 100139].
Journal: Research and practice in thrombosis and haemostasis
Published: August 21, 2023
Reply to "Comment on: A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays".
Journal: Research and practice in thrombosis and haemostasis
Published: July 11, 2023
Genetic determinants of enhanced von Willebrand factor clearance from plasma.
Journal: Journal of thrombosis and haemostasis : JTH
Published: September 27, 2022
A comparative study in patients with type 2 von Willebrand disease using 4 different platelet-dependent von Willebrand factor assays.
Journal: Research and practice in thrombosis and haemostasis
Published: July 08, 2022
Phenotypic and genetic characterizations of the Milan cohort of von Willebrand disease type 2.
Journal: Blood advances
Published: February 02, 2022
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: August 26, 2021
The ADAMTS13-von Willebrand factor axis in COVID-19 patients.
Journal: Journal of thrombosis and haemostasis : JTH
Published: July 14, 2020
Last Updated: 09/26/2026