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Haemophilia : the Official Journal of the World Federation of Hemophilia|February 29, 2020
Evaluation of a fully automated von Willebrand factor assay panel for the diagnosis of von Willebrand diseaseFrancesca Stufano, Luciano Baronciani, Paolo Bucciarelli, et al.
Haematologica|August 18, 2025
Genetic determinants of clinical variability in type 2 von Willebrand disease: bridging genotype and phenotypeOmid Seidizadeh, Alessandro Ciavarella, Luciano Baronciani, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 22, 2022
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patientsMaria Teresa Pagliari, Luciano Baronciani, Chiara Cordiglieri, et al.
Research and Practice in Thrombosis and Haemostasis|December 1, 2025
Deep molecular modeling and mechanistic insights into type 2A von Willebrand disease with von Willebrand factor A2 domain mutationsOmid Seidizadeh, Luca Mollica, Davide Giana, et al.
Research and Practice in Thrombosis and Haemostasis|May 22, 2023
A comparative study in patients with type 2 von Willebrand disease using 4 different platelet-dependent von Willebrand factor assaysPaola Colpani, Luciano Baronciani, Francesca Stufano, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patientsLuciano Baronciani, Giovanna Cozzi, Maria Teresa Canciani, et al.
Journal of Thrombosis and Haemostasis : JTH|September 30, 2020
Increasing levels of von Willebrand factor and factor VIII with age in patients affected by von Willebrand diseaseEugenia Biguzzi, Simona Maria Siboni, Saskia le Cessie, et al.
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