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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.
Pediatric Blood & Cancer|March 4, 2020
Essential thrombocythemia A retrospective case seriesAssaf Arie Barg, Amos Toren, Hannah Tamary, et al.
European Journal of Pediatrics|April 11, 2024
Symptomatic corpus luteum hemorrhage in adolescent females with ITPAlexander Yelak, Anat From, Oded Gilad, et al.
International Journal of Clinical Oncology|June 19, 2021
Delayed diagnosis and treatment of children with cancer during the COVID-19 pandemicMichal Dvori, Sarah Elitzur, Assaf Barg, et al.
European Journal of Pediatrics|July 6, 2026
Disease severity of children with hereditary spherocytosis predicts the clinical course of aplastic crisisShiri Rubin, Shira Devora Ben Ami, Ohad Atia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 10, 2018
A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorderNaama Orenstein, Hadassa Goldberg-Stern, Rachel Straussberg, et al.
British Journal of Haematology|November 20, 2023
Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2Orna Steinberg-Shemer, Joanne Yacobovich, Sharon Noy-Lotan, et al.
Pediatric Blood & Cancer|December 27, 2021
Pediatric severe factor XI deficiency: A multicenter studyAssaf Arie Barg, Sarina Levy-Mendelovich, Ivan Budnik, et al.
Pediatric Blood & Cancer|May 21, 2021
Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcomeAsaf D Yanir, Aviva Krauss, Jerry Stein, et al.
Genes|November 27, 2025
A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor PrognosisDafna Brik Simon, Yarden Greental Ness, Orly Dgany, et al.
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