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American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
The Pediatric Infectious Disease Journal|November 16, 2017
Response of Symptomatic Persistent Chronic Disseminated Candidiasis to Corticosteroid Therapy in Immunosuppressed Pediatric Patients: Case Study and Review of the LiteratureVered Shkalim-Zemer, Itzhak Levi, Salvador Fischer, et al.
Human Molecular Genetics|September 25, 2018
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)Aaron Seo, Suleyman Gulsuner, Sarah Pierce, et al.
British Journal of Haematology|October 20, 2010
A randomized phase II trial of Arginine Butyrate with standard local therapy in refractory sickle cell leg ulcersLillian McMahon, Hannah Tamary, Melissa Askin, et al.
Journal of Pediatric Hematology/Oncology|June 4, 2016
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic AnalysisOrna Steinberg-Shemer, Siobán Keel, Orly Dgany, et al.
European Journal of Haematology|February 5, 2017
Molecular diagnosis of α-thalassemia in a multiethnic populationOded Gilad, Orna Steinberg Shemer, Orly Dgany, et al.
Clinical Genetics|December 19, 2024
A Variable Clinical Presentation of Hemoglobin City of HopeDafna Brik Simon, Dvora Filon, Vardiella Meiner, et al.
Pediatric Blood & Cancer|November 7, 2024
Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated NeutropeniaLital Oz-Alcalay, Orna Steinberg-Shemer, Eyal Elron, et al.
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