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American Journal of Hematology|January 9, 2008
Response to hydroxyurea therapy in beta-thalassemiaAriel Koren, Carina Levin, Orly Dgany, 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.Journal of Pediatric Hematology/Oncology|December 14, 2006
Prolonged course of familial hemophagocytic lymphohistiocytosisOrna Steinberg, Joanne Yacobovich, Orly Dgany, et al.European Journal of Haematology|December 5, 2012
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemiaHanna Shalev, Daniela Landau, Serge Pissard, et al.Hemoglobin|September 16, 2014
Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli ArabsOded Gilad, Orly Dgany, Sharon Noy-Lotan, et al.American Journal of Hematology|June 30, 2004
Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn tripletsShmuel Arnon, Hannah Tamary, Orly Dgany, et al.Cold Spring Harbor Molecular Case Studies|July 2, 2017
Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemiaOrna Steinberg-Shemer, Jacob C Ulirsch, Sharon Noy-Lotan, et al.Frontiers in Physiology|July 8, 2021
Cdan1 Is Essential for Primitive ErythropoiesisSharon Noy-Lotan, Orly Dgany, Nathaly Marcoux, et al.Journal of Pediatric Hematology/Oncology|December 20, 2007
Congenital amegakaryocytic thrombocytopenia-3 novel c-MPL mutations and their phenotypic correlationsOrna Steinberg, Gil Gilad, Orly Dgany, et al.European Journal of Haematology|April 3, 2004
Molecular characterization of three novel Fanconi anemia mutations in Israeli ArabsHannah Tamary, Orly Dgany, Helen Toledano, et al.Pageof 5