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International Journal of Molecular Sciences|July 29, 2023
Four Decades of Carrier Detection and Prenatal Diagnosis in Hemophilia A: Historical Overview, State of the Art and Future DirectionsRima Dardik, Szymon Janczar, Shadan Lalezari, et al.Blood|February 15, 2003
Prevalence, causes, and characterization of factor XI inhibitors in patients with inherited factor XI deficiencyOphira Salomon, Ariella Zivelin, Tami Livnat, et al.Transfusion|June 8, 2012
Compound heterozygosity of HLA-DRB3*01:01 and HLA-DRB4*01:01 as a potential predictor of fetal neonatal alloimmune thrombocytopeniaRon Loewenthal, Nurit Rosenberg, Rivka Kalt, et al.Blood Cells, Molecules & Diseases|December 19, 2020
The potential role of emicizumab prophylaxis in severe von Willebrand diseaseAssaf A Barg, Einat Avishai, Ivan Budnik, et al.Journal of the American Heart Association|January 15, 2013
Leptin locally synthesized in carotid atherosclerotic plaques could be associated with lesion instability and cerebral emboliJacob Schneiderman, Katrin Schaefer, Frank D Kolodgie, et al.Pediatric Blood & Cancer|October 23, 2025
Emicizumab in Previously Untreated Patients and Minimally Treated Patients With Hemophilia A: A Comparative Study Between Two International CohortsSarina Levy-Mendelovich, Tlalit Barhod, Ivan Budnik, et al.Pediatric Blood & Cancer|November 17, 2023
Bleeding phenotype and hemostatic evaluation by thrombin generation in children with Noonan syndrome: A prospective studyAssaf A Barg, Yonatan Yeshayahu, Einat Avishai, et al.Journal of Thrombosis and Haemostasis : JTH|November 20, 2025
Endothelial protein C receptor-mediated endogenous and therapeutic transport of activated protein C across the blood-retina barrier protects the retinaTami Livnat, Ivan Budnik, Yael Nisgav, et al.Pediatric Blood & Cancer|December 27, 2021
Pediatric severe factor XI deficiency: A multicenter studyAssaf Arie Barg, Sarina Levy-Mendelovich, Ivan Budnik, et al.Pageof 6