1. Acquired FXIII deficiency and AL amyloidosis: A case of a rare association. (December 2020) Authors: Ferretti, A.; Baldacci, E.; Fazio, F.; Abbruzzese, R.; Barone, F.; De Luca, M.L.; Petrucci, M.T.; Chistolini, A.; Mazzucconi, M.G.; Santoro, C. Journal: Transfusion and apheresis science Issue: Volume 59:Number 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bleeding phenotype and correlation with factor XI (FXI) activity in congenital FXI deficiency: results of a retrospective study from a single centre. (27th January 2015) Authors: Santoro, C.; Di Mauro, R.; Baldacci, E.; De Angelis, F.; Abbruzzese, R.; Barone, F.; Bochicchio, R. A.; Ferrara, G.; Guarini, A.; Foà, R.; Mazzucconi, M. G. Journal: Haemophilia Issue: Volume 21:Number 4(2015:Jul.) Page Start: 496 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗