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Animals : an Open Access Journal From MDPI|October 27, 2022
Use of GnRH Treatment Based on Pregnancy-Associated Glyco-Proteins (PAGs) Levels as a Strategy for the Maintenance of Pregnancy in Buffalo Cows: A Field StudyCorrado Pacelli, Vittoria Lucia Barile, Emilio Sabia, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|April 26, 2018
Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and ThrombosisAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Acta Haematologica|May 13, 2020
Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413GlnAntonio Girolami, Mariano Paoletti, Silvia Ferrari, et al.
American Journal of Hematology|May 29, 2008
Congenital factor X deficiencies with a defect only or predominantly in the extrinsic or in the intrinsic system: a critical evaluationAntonio Girolami, Pamela Scarparo, Raffaella Scandellari, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 16, 2018
Cardiovascular diseases in congenital prekallikrein deficiency: comparison with other chance-associated morbiditiesAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Expert Review of Hematology|November 25, 2010
Congenital prekallikrein deficiencyAntonio Girolami, Pamela Scarparo, Nicole Candeo, et al.
Gene|July 25, 2025
Genes involved in lipid, carbohydrate and protein metabolic processes located in QTL regions affecting pork meat flavorPaola Di Gregorio, Giulia Grassi, Anna Maria Perna, et al.
Hematology (Amsterdam, Netherlands)|November 23, 2017
A structure-function analysis in patients with prekallikrein deficiencyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A new mutation (Arg251Trp) in the Ca2+ binding site of factor X protease domain appears to be responsible for the defect in the extrinsic pathway activation of factor X PaduaAntonio Girolami, Fabrizio Vianello, Laura Cabrio, et al.
Blood Cells, Molecules & Diseases|March 19, 2019
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term studyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.
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