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Ophthalmology|January 9, 2004
Nonarteritic anterior ischemic optic neuropathy is associated with a specific platelet polymorphism located on the glycoprotein Ibalpha geneOphira Salomon, Nurit Rosenberg, David M Steinberg, et al.
Pediatric Blood & Cancer|August 23, 2022
Application of a clinical decision rule and laboratory assays in pediatrics: Adult heparin-induced thrombocytopeniaOmri Cohen, Kfir Lange, Ivan Budnik, et al.
Pediatric Blood & Cancer|May 26, 2017
Quantification of specific T and B cells immunological markers in children with chronic and transient ITPSarina Levy-Mendelovich, Atar Lev, Shraga Aviner, 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.
American Journal of Obstetrics and Gynecology|December 14, 2004
The common prothrombotic factors in nulliparous women do not compromise blood flow in the feto-maternal circulation and are not associated with preeclampsia or intrauterine growth restrictionOphira Salomon, Uri Seligsohn, David M Steinberg, et al.
Human Mutation|February 8, 2006
Molecular diversity of Glanzmann thrombasthenia in southern India: new insights into mRNA splicing and structure-function correlations of alphaIIbbeta3 integrin (ITGA2B, ITGB3)Hava Peretz, Nurit Rosenberg, Meytal Landau, et al.
European Journal of Haematology|June 30, 2018
SMYD1 is the underlying gene for the AnWj-negative blood group phenotypeVered Yahalom, Nir Pillar, Yingying Zhao, et al.
Frontiers in Neurology|January 9, 2019
A Novel Compound Targeting Protease Receptor 1 Activators for the Treatment of GlioblastomaEfrat Shavit-Stein, Ehud Sheinberg, Valery Golderman, et al.
Human Mutation|June 18, 2014
Spectrum of the mutations in Bernard-Soulier syndromeAnna Savoia, Shinji Kunishima, Daniela De Rocco, et al.
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