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Minor Clinical Impact of COVID-19 Pandemic on Patients With Primary Immunodeficiency in Israel

Frontiers in immunology, 2021-01, Vol.11, p.614086-614086

2021

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First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and Insights

Frontiers in immunology, 2017-11, Vol.8, p.1448-1448

2017

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

Immunologic research, 2022-04, Vol.70 (2), p.216-223

2022

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A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia

Immunologic research, 2021-02, Vol.69 (1), p.100-106

2021

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Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With IL7RA Mutation

Frontiers in immunology, 2019-07, Vol.10, p.1672-1672

2019

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Thymic function in MHC class II–deficient patients

Journal of allergy and clinical immunology, 2013-03, Vol.131 (3), p.831-839

2013

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The Contribution of Smoking and Exposure to Tobacco Smoke to Streptococcus pneumoniae and Haemophilus influenzae Carriage in Children and Their Mothers

Clinical infectious diseases, 2006-04, Vol.42 (7), p.897-903

2006

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Relative Importance of Nasopharyngeal versus Oropharyngeal Sampling for Isolation of Streptococcus pneumoniae and Haemophilus influenzae from Healthy and Sick Individuals Varies with Age

Journal of Clinical Microbiology, 2004-10, Vol.42 (10), p.4604-4609

2004

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Beta lactam allergy in children from two ethnically different populations

Pediatrics international, 2010-02, Vol.52 (1), p.126-128

2010

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Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency

Clinical immunology (Orlando, Fla.), 2020-04, Vol.213, p.108366-108366, Article 108366

2020

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A database for immunodeficiency due to mutations in Nuclear Factor kappa B pathway genes

LymphoSign journal, 2016-11, Article lymphosign-2016-0009

Broides, Arnon

2016

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124 Neutropenia in X-linked agammaglobulinemia patients, is possibly the most common presenting sign

Clinical immunology (Orlando, Fla.), 2024-05, Vol.262, p.110066, Article 110066

2024

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

Journal of clinical immunology, 2023-02, Vol.43 (2), p.350-357

2023

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Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study

Journal of allergy and clinical immunology, 2018-03, Vol.141 (3), p.1036-1049.e5

2018

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Different manifestations of milk allergy in populations residing in the same geographic area

Pediatrics international, 2009-02, Vol.51 (1), p.162-163

2009

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Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiency

Journal of allergy and clinical immunology, 2020-03, Vol.145 (3), p.1011-1015.e6

2020

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

Immunologic research, 2022-12, Vol.70 (6), p.775-780

2022

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

Blood, 2023-11, Vol.142 (20), p.1740-1751

2023

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108 PU.1-associated inborn errors of immunity: new mutations, phenotypes, and inheritance patterns

Clinical immunology (Orlando, Fla.), 2024-05, Vol.262, p.110050, Article 110050

2024

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

Blood, 2024-09, Vol.144 (12), p.1300-1313

2024

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

European journal of paediatric neurology, 2021-05, Vol.32, p.36-39

2021

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Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients

American journal of hematology, 2017-01, Vol.92 (1), p.28-36

2017

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SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma

Journal of clinical immunology, 2023-04, Vol.43 (3), p.625-635

2023

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B-Type Natriuretic Peptide and Cardiovascular Function in Young Children With Obstructive Sleep Apnea

Chest, 2010-09, Vol.138 (3), p.528-535

2010

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Subclinical intestinal inflammation in chronic granulomatous disease patients

Immunologic research, 2016-02, Vol.64 (1), p.155-159

2016

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Minor Clinical Impact of COVID-19 Pandemic on Patients With Primary Immunodeficiency in Israel

First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and Insights

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

A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia

Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With IL7RA Mutation

Thymic function in MHC class II–deficient patients

The Contribution of Smoking and Exposure to Tobacco Smoke to Streptococcus pneumoniae and Haemophilus influenzae Carriage in Children and Their Mothers

Relative Importance of Nasopharyngeal versus Oropharyngeal Sampling for Isolation of Streptococcus pneumoniae and Haemophilus influenzae from Healthy and Sick Individuals Varies with Age

Beta lactam allergy in children from two ethnically different populations

Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency

A database for immunodeficiency due to mutations in Nuclear Factor kappa B pathway genes

124 Neutropenia in X-linked agammaglobulinemia patients, is possibly the most common presenting sign

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

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study

Different manifestations of milk allergy in populations residing in the same geographic area

Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiency

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

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

108 PU.1-associated inborn errors of immunity: new mutations, phenotypes, and inheritance patterns

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

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

Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients

SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma

B-Type Natriuretic Peptide and Cardiovascular Function in Young Children With Obstructive Sleep Apnea

Subclinical intestinal inflammation in chronic granulomatous disease patients

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