Arnon Broides

Beersheba, D, Israel

Last Updated: 09/26/2026

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Found 48 publications

Comprehensive Profiling of T- and B-Cell Receptor Repertoires Demonstrates Impaired Developmental and Activation of Adaptive Immunity in DOCK8 Deficiency.

Comprehensive Profiling of T- and B-Cell Receptor Repertoires Demonstrates Impaired Developmental and Activation of Adaptive Immunity in DOCK8 Deficiency.

Journal: Journal of clinical immunology

Published: July 01, 2025

Respiratory Manifestations in Pediatric Patients With Interleukin 6 Receptor Deficiency.

Respiratory Manifestations in Pediatric Patients With Interleukin 6 Receptor Deficiency.

Journal: Pediatric pulmonology

Published: March 12, 2025

One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them.

One hundred thirty-four germ line PU.1 variants and the agammaglobulinemic patients carrying them.

Journal: Blood

Published: September 09, 2024

Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohort.

Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohort.

Journal: Blood

Published: November 27, 2023

Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signaling.

Loss of function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signaling.

Journal: Blood

Published: April 05, 2023

SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma.

SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma.

Journal: Journal of clinical immunology

Published: October 02, 2022

Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.

Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.

Journal: Journal of clinical immunology

Published: June 27, 2022

Hyper IgM in tricho-hepato-enteric syndrome due to TTC37 mutation.

Hyper IgM in tricho-hepato-enteric syndrome due to TTC37 mutation.

Journal: Immunologic research

Published: March 30, 2022

Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in Israel.

Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in Israel.

Journal: The journal of allergy and clinical immunology. In practice

Published: December 09, 2021

B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemia.

B cell repertoire in patients with a novel BTK mutation: expanding the spectrum of atypical X-linked agammaglobulinemia.

Journal: Immunologic research

Published: October 25, 2021

Phenotypic variability in patients with unique double homozygous mutations causing variant ataxia telangiectasia.

Phenotypic variability in patients with unique double homozygous mutations causing variant ataxia telangiectasia.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: December 23, 2020

Trough Concentrations of Specific Antibodies in Primary Immunodeficiency Patients Receiving Intravenous Immunoglobulin Replacement Therapy.

Trough Concentrations of Specific Antibodies in Primary Immunodeficiency Patients Receiving Intravenous Immunoglobulin Replacement Therapy.

Journal: Journal of clinical medicine

Published: November 26, 2020

Showing 1-12 of 48

Last Updated: 09/26/2026