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  The key to fibrinolysis and thrombolysis

  Roger Lijnen, Désiré Collen

  09-09-2025

  https://doi.org/10.4081/btvb.2025.368

  235

  PDF: 57

  HTML: 36
• 

  Impaired platelet function in Hermansky-Pudlak syndrome associated with novel mutations in HPS3, HPS6 and HPS8 genes

  Lisa Pieri, Silvia Linari, Francesca Salvianti, Monica Attanasio, Giancarlo Castaman

  27-11-2024

  https://doi.org/10.4081/btvb.2024.150

  814

  PDF: 212
• 

  A case of acquired factor XIII deficiency secondary to plasmablastic lymphoma

  Vincenzo Sammartano, Adele Santoni, Elisabetta Zappone, Paola Calzoni, Daniela Fineschi, Eleonora Franceschini, Federico Caroni, Anna Sicuranza, Monica Bocchia, Luca Puccetti

  09-03-2023

  https://doi.org/10.4081/btvb.2023.53

  764

  PDF: 372
• 

  Recent advances in classic heparin-induced thrombocytopenia (HIT), autoimmune HIT, spontaneous HIT, and vaccine-induced immune thrombotic thrombocytopenia

  Bianca Clerici, Mariangela Scavone, Gian Marco Podda

  20-06-2024

  https://doi.org/10.4081/btvb.2024.127

  2073

  PDF: 556
• 

  Allopurinol-induced acquired von Willebrand syndrome

  Juan Eirís, Marina Suárez-Terrón, Pablo Granados, David Martínez-Campuzano, Ana Rosa Cid, Saturnino Haya, Santiago Bonanad

  25-10-2023

  https://doi.org/10.4081/btvb.2023.88

  1671

  PDF: 210
• 

  The intriguing association between cancer and congenital bleeding disorders

  Ezio Zanon

  16-12-2024

  https://doi.org/10.4081/btvb.2024.146

  256

  PDF: 77
• 

  Safety of COVID-19 mRNA vaccination in patients with history of acquired hemophilia A: a case series

  Luca Puccetti, Vincenzo Sammartano, Federico Caroni, Margherita Malchiodi, Paola Calzoni, Eleonora Franceschini, Lucrezia Galasso, Monica Bocchia

  17-10-2022

  https://doi.org/10.4081/btvb.2022.40

  2466

  PDF: 263
• 

  ReDIP, the Italian network for the diagnosis of congenital platelet function disorders

  Marco Cattaneo, Claudia Ghali, Mariangela Scavone

  22-04-2024

  https://doi.org/10.4081/btvb.2024.134

  406

  PDF: 138
• 

  The evolution of hemostasis genetics: from monogenic disorders to complex traits. A historical perspective

  Augusto Di Castelnuovo

  01-07-2025

  https://doi.org/10.4081/btvb.2025.184

  835

  PDF: 141
• 

  Addressing some challenges of congenital fibrinogen disorders in 2023 and beyond

  Cristina Santoro, Alessandro Casini

  03-08-2023

  https://doi.org/10.4081/btvb.2023.75

  1219

  PDF: 313

• CS07 | Endothelial dysfunction and impaired angiogenesis in Hermansky-Pudlak syndrome (HPS) type 1: studies with endothelial colony forming cells F. Tondi¹, G. Purgatorio¹, C. Sgromo², E. Giglio¹, E. Petito¹, E. Falcinelli¹, G. Guglielmini¹, A. Follenzi², P. Gresele¹, L. Bury^1*, C. Olgasi^3* | ^*Shared senior authorship; ¹Department of Medicine and Surgery, Section of Internal and Cardiovascular Medicine, University of Perugia; ²Department of Health Sciences, School of Medicine, University of Piemonte Orientale, Novara; ³Department of Translational Medicine, School of Medicine, University of Piemonte Orientale, Novara, Italy

  16-09-2025

  https://doi.org/10.4081/btvb.2025.204

  50
• 

  Comments on “Safe and effective anticoagulation use: case studies in anticoagulation stewardship”

  Marco Marietta, Giancarlo Castaman

  01-07-2025

  https://doi.org/10.4081/btvb.2025.180

  1255

  PDF: 406
• 

  The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art

  Giovanni Di Minno, Gaia Spadarella, Ilenia Lorenza Calcaterra, Giancarlo Castaman, Paolo Simioni, Raimondo De Cristofaro, Cristina Santoro, Flora Peyvandi, Matteo Di Minno

  04-09-2024

  https://doi.org/10.4081/btvb.2024.144

  1021

  PDF: 221

  SUPPLEMENTARY MATERIAL: 103
• 

  Gene transfer in hemophilia B: a big step forward

  Giancarlo Castaman

  17-05-2023

  https://doi.org/10.4081/btvb.2023.70

  941

  PDF: 333
• 

  Thrombosis and hemostasis at the University of Padua: a reappraisal on the occasion of its 800th year of history

  Paolo Simioni, Vittorio Pengo, Paolo Prandoni

  07-11-2022

  https://doi.org/10.4081/btvb.2022.52

  2123

  PDF: 250