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• CO35 | Bleeding phenotype characterization in patients with congenital bleeding disorders: a multigenic approach using next generation sequencing to identify coagulation-modulating variants C. Simion, L. Gianesello, C. Bulato, A. Benetti, E. Campello, A. Giannella, G. Ceolotto, E. Zanon, L. Spiezia, P. Simioni | Department of Medicine – DIMED, University of Padua, Italy

  22-10-2025

  https://doi.org/10.4081/btvb.2025.242

  503

  PDF: 6
• 

  The key to fibrinolysis and thrombolysis

  Roger Lijnen, Désiré Collen

  09-09-2025

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

  1633

  PDF: 498

  HTML: 240

• CO40 | The co-inheritance of two ITGB3 variants exerting additive detrimental effects on platelets leads to variant Glanzmann thrombasthenia N. Arndt¹, E. Falcinelli¹, A. Zamora-Cánovas², A. Sánchez Fuentes², A. Marín-Quilez², I. Tano¹, M.D.M. Nieto-Hernández³, J.M. Bastida⁴, J. Rivera², P. Gresele¹, L. Bury¹ | ¹Department of Medicine and Surgery, Section of Internal and Cardiovascular Medicine, University of Perugia, Italy; ²Servicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB-Pascual Parrilla, ISCIII-CIBERER, Murcia, Spain; ³Servicio de Hematología, Hospital Universitario de Jaen, Spain; ⁴Departamento de Hematología, Complejo Asistencial Universitario de Salamanca “CAUSA”, Instituto de Investigación Biomédica de Salamanca “IBSAL”, Centro de Investigación del Cáncer, IBMCC-CSIC, Universidad de Salamanca “USAL”, Salamanca, Spain

  22-10-2025

  https://doi.org/10.4081/btvb.2025.247

  568

  PDF: 2

• CO13 | Genetic background in hypercholesterolemic patients framing cardiovascular risk A. Kura¹, E. Sticchi², G. Barbieri¹, R. Orsi¹, S. Suraci¹, G.M. Scaturro³, E. Lotti⁴, F. Crudele⁴, M. Berteotti², A.M. Gori², R. Marcucci², B. Giusti² | ¹Department of Experimental and Clinical Medicine, Firenze; ²Department of Experimental and Clinical Medicine, Atherothrombotic Diseases Center, Careggi Hospital, Firenze; ³Meyer Children’s Hospital IRCCS, Firenze; ⁴Atherothrombotic Diseases Center, Careggi Hospital, Firenze, Italy

  22-10-2025

  https://doi.org/10.4081/btvb.2025.217

  658

  PDF: 5

• CO26 | Relationship between SMAD3 variants and non-aortic cardiovascular features L. Squillantini, E. Sticchi, P. Cantini, S. Suraci, A. Rogolino, F. Gensini, S. Nistri, G. Pepe, A.M. Gori, M. Berteotti, R. Marcucci, B. Giusti | Università degli Studi di Firenze, Dipartimento di Medicina Sperimentale e Clinica, Firenze, Italy

  22-10-2025

  https://doi.org/10.4081/btvb.2025.232

  557

  PDF: 1

• CS06 | Patient specific iPSCs-derived sinusoidal endothelial cells for phenotypic correction of haemophilia A A. Benetti¹, C.M. Radu¹, C. Samà¹, M. Trevisan², C. Simion¹, E. Campello¹, P. Simioni¹ | ¹Department of Medicine - DIMED, Padua University Hospital; ²Department of Molecular Medicine, University of Padua, Italy

  22-10-2025

  https://doi.org/10.4081/btvb.2025.203

  688

  PDF: 3
• 

  Pharmacokinetics of extended half-life albumin-fused factor IX and heterogeneous F9 variants in hemophilia B: a retrospective cohort study

  Barbara Lunghi, Massimo Morfini, Silvia Linari, Dario Balestra, Alessio Branchini, Lisa Pieri, Donata Belvini, Laura Banov, Cristina Santoro, Giancarlo Castaman, Francesco Bernardi

  02-03-2026

  https://doi.org/10.4081/btvb.2026.413

  379

  PDF: 120

  Supplementary: 87
• 

  Expanding the genetic landscape of hereditary thrombophilia: classical defects, novel variants, and genomic perspectives. A narrative review

  Chiara Simion, Elena Campello, Walter Ageno, Paolo Simioni

  28-08-2026

  https://doi.org/10.4081/btvb.2026.427

  268

  PDF: 58

  SUPPLEMENTARY FILES: 31
• 

  Whole exome sequencing in a family with thromboangiitis obliterans

  Barbara Lunghi, Dario Balestra, Nicole Ziliotto, Giulia Pavani, Matteo Bovolenta, Patrizia Della Valle, Mirko Pinotti, Giovanna Marchetti, Armando D'Angelo, Francesco Bernardi

  28-08-2026

  https://doi.org/10.4081/btvb.2026.367

  236

  PDF: 38

  SUPPLEMENTARY FILES: 25
• 

  Impact of CYP2C19 loss-of-function variants on outcomes in atrial fibrillation patients undergoing percutaneous coronary intervention: rationale and study design of the WOEST-3 genetic substudy

  Simona Chiusolo, Ashley Verburg, Carmela Morizzo, Ron H.N. Van Schaik, Maja Matic, Marieke J.H. Coenen, Michael Maeng, Jurrien ten Berg, Raffaele De Caterina

  28-08-2026

  https://doi.org/10.4081/btvb.2026.421

  294

  PDF: 32

  APPENDIX: 22
• 

  PO61 | RISK FACTORS FOR INTRACRANIAL HEMORRHAGE: AN UMBRELLA REVIEW TO INFORM MACHINE LEARNING PREDICTION MODELS IN GLIOMA PATIENTS RECEIVING ANTICOAGULATION T.A. Adeyemo, S. Greenley, F. Ware, W. Jones, A. Maraveyas, F. Haque | ¹Centre of Excellence for Data Science, Artificial Intelligence and Modelling DAIM, Faculty of Science and Engineering, University of Hull, UK; ²Hull York Medical School, Hull, UK; ³Academic Library Services, University of Hull, UK; ⁴NHS Humber Health Partnership, Hull, UK

  ICTHIC 2026

  16-04-2026

  https://doi.org/10.4081/btvb.2026.552

  423

  PDF: 100
• 

  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

  1536

  PDF: 330
• 

  Diagnostic and management practices for inherited fibrinogen disorders: a nationwide survey of Italian Hemophilia Treatment Centers

  Renato Marino, Silvia Linari, Marzia Leotta, Antonio Coppola, Chiara Biasoli, Maria Elisa Mancuso, Flora Peyvandi, Cristina Santoro, Ezio Zanon, Rita Carlotta Santoro

  02-12-2025

  https://doi.org/10.4081/btvb.2025.372

  824

  PDF: 102

  HTML: 108

  Supplementary: 64

  Appendix: 70

• PO61 | ACTN1-related thrombocytopenia and severe hyperhomocysteinemia: a case report A. Pozzi, G. Rosati, M. Padrini, S. Laurenti, G. Ferrari, R.M. Medici, C. Barale, I. Russo, A. Morotti | University of Turin, San Luigi Hospital, Orbassano (TO), Italy

  22-10-2025

  https://doi.org/10.4081/btvb.2025.330

  531

  PDF: 3

• PO51 | Thrombocythemia associated with a non-canonical JAK2 mutation: a case report G. Rosati, A. Pozzi, M. Padrini, S. Laurenti, G. Ferrari, R.M. Medici, C. Barale, I. Russo, A. Morotti | University of Turin, AUO San Luigi Gonzaga, Orbassano (TO), Italy

  22-10-2025

  https://doi.org/10.4081/btvb.2025.320

  709

  PDF: 2
• 

  The subtle red line between combating and resolving inflammation in the cardiovascular disease, a “silent sniper”

  Ciarán Kennedy, Luke J. Conroy, Braden Millar, Monica de Gaetano

  30-06-2025

  https://doi.org/10.4081/btvb.2025.187

  1566

  PDF: 425

• PO03 | Enlarged platelets with reduced GP IB/IX can indicate disorders other than Bernard-Soulier syndrome C. Zaninetti¹, A. Marín-Quilez², S. Semenowitsch¹, A. Sánchez-Fuentes², A. Zamora-Cánovas², P. Gómez-González², E. Birgitte Leinøe³, N. Fernández-Mosteirin⁴, T. Murciano^5,6, C. Freyer¹, T. Thiele¹, J. Rivera^2,7, A. Greinacher¹ | ¹Universitätsmedizin Greifswald, Institut Für Transfusionsmedizin, Greifswald, Germany; ²Universidad De Murcia, Servicio De Hematología, Hospital Universitario Morales Meseguer, Centro Regional De Hemodonacion, Imib-Pascual Parrilla, Ciberer-U765, Murcia, Spain; ³Rigshospitalet University Hospital, Department of Haematology and Department of Genomic Medicine, Copenhagen, Denmark; ⁴Hospital Universitario Miguel Servet, Servicio De Hematología, Zaragoza, Spain; ⁵Hospital Universitario Vall D’Hebron, Servicio De Oncología y Hematología Pediatricas; ⁶Vall D’Hebron Institut De Recerca, Barcelona, Spain; ⁷Grupo Español De Alteraciones Plaquetarias Congénitas, Murcia, Spain

  22-10-2025

  https://doi.org/10.4081/btvb.2025.265

  534

  PDF: 2