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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 4, 2008
Correlation of vascular endothelial growth factor with the severity of thalassemia intermediaDavid Shitrit, Hannah Tamary, Ariel Koren, et al.Journal of Pediatric Surgery|April 19, 2011
Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature reviewOfer Schiller, Shifra Ash, Tommy Schonfeld, et al.Journal of Pediatric Hematology/Oncology|December 20, 2012
Anemia associated with acute infection in children: an animal modelAmi Ballin, Aeed Hussein, Hananya Vaknine, et al.American Journal of Hematology|January 9, 2008
Response to hydroxyurea therapy in beta-thalassemiaAriel Koren, Carina Levin, Orly Dgany, et al.Prenatal Diagnosis|January 6, 2010
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropeniaMira Malcov, Adi Reches, Dalit Ben-Yosef, et al.Acta Haematologica|January 22, 2011
E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type IIAchiya Amir, Orly Dgany, Tanya Krasnov, et al.Pediatric Hematology and Oncology|June 19, 2004
Central venous line thrombosis in children and young adults with thalassemia majorYaron Finkelstein, Isaac Yaniv, Michael Berant, et al.The Hematology Journal : the Official Journal of the European Haematology Association|May 17, 2003
Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 geneAlexis Proust, Lydie Da Costa, Patricia Rince, et al.BMC Molecular and Cell Biology|April 16, 2020
Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I diseaseGrace Swickley, Yehoshua Bloch, Lidor Malka, et al.Journal of Pediatric Hematology/Oncology|December 14, 2006
Prolonged course of familial hemophagocytic lymphohistiocytosisOrna Steinberg, Joanne Yacobovich, Orly Dgany, et al.Pageof 13