Dafna Simon-Brik

14 Kaplan St, 4920235
Petah Tiqwa, M 49202, Israel

Last Updated: 09/26/2026

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Found 12 publications

Disease severity of children with hereditary spherocytosis predicts the clinical course of aplastic crisis.

Disease severity of children with hereditary spherocytosis predicts the clinical course of aplastic crisis.

Journal: European journal of pediatrics

Published: April 22, 2026

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.

Journal: Genes

Published: August 22, 2025

A Variable Clinical Presentation of Hemoglobin City of Hope.

A Variable Clinical Presentation of Hemoglobin City of Hope.

Journal: Clinical genetics

Published: September 27, 2024

Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated Neutropenia.

Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated Neutropenia.

Journal: Pediatric blood & cancer

Published: June 16, 2024

Symptomatic corpus luteum hemorrhage in adolescent females with ITP.

Symptomatic corpus luteum hemorrhage in adolescent females with ITP.

Journal: European journal of pediatrics

Published: February 17, 2024

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.

Journal: European journal of haematology

Published: December 19, 2023

Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.

Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.

Journal: British journal of haematology

Published: August 28, 2023

Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE-related immune thrombocytopenia.

Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE-related immune thrombocytopenia.

Journal: Pediatric blood & cancer

Published: August 22, 2023

Early response markers predict survival after etoposide-based therapy of hemophagocytic lymphohistiocytosis.

Early response markers predict survival after etoposide-based therapy of hemophagocytic lymphohistiocytosis.

Journal: Blood advances

Published: April 24, 2023

DEMOGRAPHIC, CLINICAL AND LABORATORY CHARACTERISTICS OF CHILDREN DIAGNOSED WITH HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH) IN THE SCHNEIDER CHILDREN'S MEDICAL CENTER BETWEEN 2004-2020

DEMOGRAPHIC, CLINICAL AND LABORATORY CHARACTERISTICS OF CHILDREN DIAGNOSED WITH HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH) IN THE SCHNEIDER CHILDREN'S MEDICAL CENTER BETWEEN 2004-2020

Journal: Harefuah

Published: January 30, 2023

Japanese scoring systems to predict resistance to intravenous immunoglobulin in Kawasaki disease were unreliable for Caucasian Israeli children.

Japanese scoring systems to predict resistance to intravenous immunoglobulin in Kawasaki disease were unreliable for Caucasian Israeli children.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: January 12, 2018

High-dose aspirin for Kawasaki disease: outdated myth or effective aid?

High-dose aspirin for Kawasaki disease: outdated myth or effective aid?

Journal: Clinical and experimental rheumatology

Published: July 20, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026