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Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2)

Journal of allergy and clinical immunology, 2020-06, Vol.145 (6), p.1664-1672.e10

2020

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Validation of the psoriasis epidemiology screening tool (PEST) and the new early arthritis for psoriatic patients (EARP) in pediatric population: pilot study

Clinical rheumatology, 2022-04, Vol.41 (4), p.1125-1130

2022

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Colchicine treatment can be discontinued in a selected group of pediatric FMF patients

Pediatric rheumatology online journal, 2023-01, Vol.21 (1), p.2-2, Article 2

2023

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Pediatric Psoriasis with or without Arthritis: Does It Make a Difference?

Journal of clinical medicine, 2023-12, Vol.13 (1), p.242

2023

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Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom

Italian journal of pediatrics, 2022-06, Vol.48 (1), p.84-84, Article 84

2022

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Effect of interleukin-1 antagonist on growth of children with colchicine resistant or intolerant FMF

Pediatric rheumatology online journal, 2023-01, Vol.21 (1), p.4-4, Article 4

2023

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Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature

BMC medical genetics, 2019-03, Vol.20 (1), p.53-53, Article 53

2019

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Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies

Pediatric rheumatology online journal, 2019-07, Vol.17 (1), p.52-52, Article 52

2019

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Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders

Frontiers in genetics, 2023-01, Vol.13, p.1018062-1018062

2023

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Impaired receptor editing and heterozygous RAG2 mutation in a patient with systemic lupus erythematosus and erosive arthritis

Journal of allergy and clinical immunology, 2015-01, Vol.135 (1), p.272-273

2015

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Do geography and ethnicity play a role in juvenile Spondyloarthritis? A multi-center binational retrospective study

Pediatric rheumatology online journal, 2021-01, Vol.19 (1), p.4-8, Article 4

2021

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A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome

Journal of allergy and clinical immunology, 2012-12, Vol.130 (6), p.1414-1416

2012

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Case Series of Myocarditis Following mRNA COVID Vaccine Compared to Pediatric Multisystem Inflammatory Syndrome: Multicenter Retrospective Study

Vaccines (Basel), 2022-07, Vol.10 (8), p.1207

2022

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Psychological tendencies of children with juvenile idiopathic arthritis

Scandinavian journal of psychology, 2022-12, Vol.63 (6), p.624-633

2022

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Poststreptococcal Myalgia and Protracted Febrile Myalgia Syndrome: Similar Yet Different

The Journal of pediatrics, 2022-08, Vol.247, p.163-167.e2

2022

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Small Fiber Neuropathy as a Presenting Symptom of Juvenile Systemic Lupus Erythematosus

The Israel Medical Association journal, 2022-08, Vol.24 (8), p.544-545

2022

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Performance of 2019 EULAR/ACR classification criteria for systemic lupus erythematosus in a paediatric population-a multicentre study

Rheumatology (Oxford, England), 2021-11, Vol.60 (11), p.5142-5148

2021

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Obstacles in Early Diagnosis of Children With Juvenile Idiopathic Arthritis: A Nationwide Israeli Retrospective Study

Journal of rheumatology, 2023-06, Vol.50 (6), p.799

2023

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Clinical significance of E148Q heterozygous variant in paediatric familial Mediterranean fever

Rheumatology (Oxford, England), 2021-11, Vol.60 (11), p.5447-5451

2021

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An “On Demand” canakinumab regimen for treating children with Colchicine-Resistant familial Mediterranean fever – A multicentre study

International immunopharmacology, 2024-05, Vol.132, p.111967-111967, Article 111967

2024

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

Pediatric blood & cancer, 2024-05, Vol.71 (5), p.e30911-e30911

2024

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Small Vessel Vasculitis of the Central Nervous System: A Rare Disease with a Challenging Diagnosis

The Israel Medical Association journal, 2021-10, Vol.23 (10), p.672-673

2021

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Recombination activity of human recombination-activating gene 2 (RAG2) mutations and correlation with clinical phenotype

Journal of allergy and clinical immunology, 2019-02, Vol.143 (2), p.726-735

2019

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Efficacy and Safety of Canakinumab in Patients With Systemic Juvenile Idiopathic Arthritis With and Without Fever at Baseline: Results From an Open‐Label, Active‐Treatment Extension Study

Arthritis & rheumatology (Hoboken, N.J.), 2020-12, Vol.72 (12), p.2147-2158

2020

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IgG Fc glycosylation as an axis of humoral immunity in childhood

Journal of allergy and clinical immunology, 2020-02, Vol.145 (2), p.710-713.e9

2020

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Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2)

Validation of the psoriasis epidemiology screening tool (PEST) and the new early arthritis for psoriatic patients (EARP) in pediatric population: pilot study

Colchicine treatment can be discontinued in a selected group of pediatric FMF patients

Pediatric Psoriasis with or without Arthritis: Does It Make a Difference?

Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom

Effect of interleukin-1 antagonist on growth of children with colchicine resistant or intolerant FMF

Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature

Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies

Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders

Impaired receptor editing and heterozygous RAG2 mutation in a patient with systemic lupus erythematosus and erosive arthritis

Do geography and ethnicity play a role in juvenile Spondyloarthritis? A multi-center binational retrospective study

A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome

Case Series of Myocarditis Following mRNA COVID Vaccine Compared to Pediatric Multisystem Inflammatory Syndrome: Multicenter Retrospective Study

Psychological tendencies of children with juvenile idiopathic arthritis

Poststreptococcal Myalgia and Protracted Febrile Myalgia Syndrome: Similar Yet Different

Small Fiber Neuropathy as a Presenting Symptom of Juvenile Systemic Lupus Erythematosus

Performance of 2019 EULAR/ACR classification criteria for systemic lupus erythematosus in a paediatric population-a multicentre study

Obstacles in Early Diagnosis of Children With Juvenile Idiopathic Arthritis: A Nationwide Israeli Retrospective Study

Clinical significance of E148Q heterozygous variant in paediatric familial Mediterranean fever

An “On Demand” canakinumab regimen for treating children with Colchicine-Resistant familial Mediterranean fever – A multicentre study

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

Small Vessel Vasculitis of the Central Nervous System: A Rare Disease with a Challenging Diagnosis

Recombination activity of human recombination-activating gene 2 (RAG2) mutations and correlation with clinical phenotype

Efficacy and Safety of Canakinumab in Patients With Systemic Juvenile Idiopathic Arthritis With and Without Fever at Baseline: Results From an Open‐Label, Active‐Treatment Extension Study

IgG Fc glycosylation as an axis of humoral immunity in childhood

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