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Blood Cells, Molecules & Diseases|March 12, 2021
Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patientsNurit Rosenberg, Rima Dardik, Hagit Hauschner, et al.Pediatric Blood & Cancer|April 12, 2011
Steroid therapy may be effective in augmenting hemoglobin levels during hemolytic crises in children with hereditary spherocytosisAmi Ballin, Orit Waisbourd-Zinman, Hitam Saab, 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.European Journal of Haematology|January 19, 2005
Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patientsShlomit Shalitin, Doron Carmi, Naomi Weintrob, et al.European Journal of Haematology|October 26, 2012
High levels of soluble serum hemojuvelin in patients with congenital dyserythropoietic anemia type IHanna Shalev, Galit Perez-Avraham, Joseph Kapelushnik, et al.Blood|October 1, 2008
Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type IHannah Tamary, Hanna Shalev, Galit Perez-Avraham, 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.Journal of Pediatric Hematology/Oncology|September 10, 2002
Congenital dyserythropoietic anemia, type 1, in a polynesian patient: response to interferon alpha2bLaurent Roda, Jérôme Pasche, Alain Fournier, 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.Platelets|January 7, 2017
Evaluating platelet function disorders in children with bleeding tendency - A single center studyOsama Tanous, Orna Steinberg Shemer, Joanne Yacobovich, et al.Pageof 13