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Archives of Disease in Childhood. Fetal and Neonatal Edition|March 8, 2002
Deposition of whole blood platelets on extracellular matrix under flow conditions in preterm infantsN Linder, B Shenkman, E Levin, et al.Journal of Thrombosis and Haemostasis : JTH|April 16, 2015
Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small-platelet thrombocytopeniaC Levin, A Koren, E Pretorius, et al.Journal of Thrombosis and Haemostasis : JTH|December 20, 2005
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombastheniaN Rosenberg, H Hauschner, H Peretz, et al.Cerebrovascular Diseases (Basel, Switzerland)|February 29, 2008
Aspirin responsiveness in acute brain ischaemia: association with stroke severity and clinical outcomeY Schwammenthal, R Tsabari, B Shenkman, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|August 14, 1999
Plasma glutathione peroxidase deficiency and platelet insensitivity to nitric oxide in children with familial strokeG Kenet, J Freedman, B Shenkman, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 15, 2018
In vitro characterization of MOD-5014, a novel long-acting carboxy-terminal peptide (CTP)-modified activated FVIIA Bar-Ilan, T Livnat, M Hoffmann, et al.Pageof 5