Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency
Article in Thrombosis Journal (January 2023)
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Homozygous SERPINC1 Mutation in Congenital Antithrombin Deficiency: A Unique First Case of Neonatal Cardiac Thrombosis
Article in Perinatology (January 2023)
The Fight against Cancer by Microgravity: The Multicellular Spheroid as a Metastasis Model
Article in International Journal of Molecular Sciences (March 2022)