Noa Shorer-Mandel
Haifa, HA, Israel
Last Updated: 09/26/2026
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Found 10 publications
Antiphospholipid Syndrome in Identical Pediatric Twins.
Journal: The Journal of rheumatology
Published: April 01, 2026
Antiphospholipid Syndrome in Identical Pediatric Twins.
Journal: The Journal of rheumatology
Published: April 01, 2026
A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.
Journal: Genes
Published: August 22, 2025
Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.
Journal: European journal of haematology
Published: December 19, 2023
PERIOPERATIVE MANAGEMENT OF AN ADOLESCENT GIRL WITH SEVERE FACTOR XI DEFICIENCY AND INHIBITORS
Journal: Harefuah
Published: January 30, 2023
Cerebral Sinovenous Thrombosis in Infants and Children: A Practical Approach to Management.
Journal: Seminars in pediatric neurology
Published: June 28, 2022
Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series.
Journal: Pediatric blood & cancer
Published: January 31, 2022
Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.
Journal: Haematologica
Published: September 30, 2021
Pediatric severe factor XI deficiency: A multicenter study.
Journal: Pediatric blood & cancer
Published: September 29, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026