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SARS-CoV-2-Induced Kawasaki-Like Hyperinflammatory Syndrome: A Novel COVID Phenotype in Children

Pediatrics (Evanston), 2020-08, Vol.146 (2), p.1

2020

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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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Defining Kawasaki disease and pediatric inflammatory multisystem syndrome-temporally associated to SARS-CoV-2 infection during SARS-CoV-2 epidemic in Italy: results from a national, multicenter survey

Pediatric rheumatology online journal, 2021-03, Vol.19 (1), p.29-29, Article 29

2021

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A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP

The Journal of experimental medicine, 2012-01, Vol.209 (1), p.29-34

2012

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Whole-exome sequencing identifies tetratricopeptide repeat domain 7A ( TTC7A ) mutations for combined immunodeficiency with intestinal atresias

Journal of allergy and clinical immunology, 2013-09, Vol.132 (3), p.656-664.e17

2013

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NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential

Clinical immunology (Orlando, Fla.), 2020-01, Vol.210, p.108309-108309, Article 108309

2020

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Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

Frontiers in immunology, 2019-04, Vol.10, p.316-316

2019

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Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

Journal of clinical immunology, 2020-08, Vol.40 (6), p.851-860

2020

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Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome

The Journal of pediatrics, 2014-06, Vol.164 (6), p.1475-1480.e2

2014

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Mulibrey nanism and immunological complications: a comprehensive case report and literature review

Frontiers in immunology, 2023-12, Vol.14, p.1303251-1303251

2023

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Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy in Two Siblings: Same Mutations but Very Different Phenotypes

Genes, 2021-01, Vol.12 (2), p.169

2021

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Premature Senescence and Increased Oxidative Stress in the Thymus of Down Syndrome Patients

Frontiers in immunology, 2021-06, Vol.12, p.669893-669893

2021

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Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network

Frontiers in immunology, 2019-08, Vol.10, p.1908-1908

2019

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Clinical Features at Onset and Genetic Characterization of Pediatric and Adult Patients with TNF-α Receptor—Associated Periodic Syndrome (TRAPS): A Series of 80 Cases from the AIDA Network

Mediators of inflammation, 2020, Vol.2020, p.1-12

2020

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Circulating Follicular Helper and Follicular Regulatory T Cells Are Severely Compromised in Human CD40 Deficiency: A Case Report

Frontiers in immunology, 2018-08, Vol.9, p.1761-1761

2018

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MIS-C Treatment: Is IVIG Always Necessary?

Frontiers in pediatrics, 2021-11, Vol.9, p.753123-753123

2021

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Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome

Allergy, asthma, and clinical immunology, 2023-04, Vol.19 (1), p.32-32, Article 32

2023

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Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot

Journal of genetics, 2021-04, Vol.100 (1), Article 5

2021

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Familial segregation of group B streptococcal infection in a consanguineous kindred

International journal of infectious diseases, 2016-10, Vol.51 (C), p.22-24

2016

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Prevalence of familial autoimmune diseases in juvenile idiopathic arthritis: results from the international Pharmachild registry

Pediatric rheumatology online journal, 2022-11, Vol.20 (1), p.103-103, Article 103

2022

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B-cell development and functions and therapeutic options in adenosine deaminase–deficient patients

Journal of allergy and clinical immunology, 2014-03, Vol.133 (3), p.799-806.e10

2014

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Outcomes of MIS-C patients treated with anakinra: a retrospective multicenter national study

Frontiers in pediatrics, 2023-08, Vol.11, p.1137051-1137051

2023

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Discordance between Clinical and Ultrasound Examinations in Juvenile Idiopathic Arthritis: An Experimental Approach

Children (Basel), 2022-03, Vol.9 (3), p.333

2022

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Corrigendum: MIS-C Treatment: Is IVIG Always Necessary?

Frontiers in pediatrics, 2022-02, Vol.9, p.826518-826518

2022

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SARS-CoV-2-Induced Kawasaki-Like Hyperinflammatory Syndrome: A Novel COVID Phenotype in Children

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

Defining Kawasaki disease and pediatric inflammatory multisystem syndrome-temporally associated to SARS-CoV-2 infection during SARS-CoV-2 epidemic in Italy: results from a national, multicenter survey

A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP

Whole-exome sequencing identifies tetratricopeptide repeat domain 7A ( TTC7A ) mutations for combined immunodeficiency with intestinal atresias

NFKB2 regulates human Tfh and Tfr pool formation and germinal center potential

Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome

Mulibrey nanism and immunological complications: a comprehensive case report and literature review

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy in Two Siblings: Same Mutations but Very Different Phenotypes

Premature Senescence and Increased Oxidative Stress in the Thymus of Down Syndrome Patients

Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network

Clinical Features at Onset and Genetic Characterization of Pediatric and Adult Patients with TNF-α Receptor—Associated Periodic Syndrome (TRAPS): A Series of 80 Cases from the AIDA Network

Circulating Follicular Helper and Follicular Regulatory T Cells Are Severely Compromised in Human CD40 Deficiency: A Case Report

MIS-C Treatment: Is IVIG Always Necessary?

Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job's syndrome

Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot

Role of Colchicine Treatment in Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS): Real-Life Data from the AIDA Network

Familial segregation of group B streptococcal infection in a consanguineous kindred

Prevalence of familial autoimmune diseases in juvenile idiopathic arthritis: results from the international Pharmachild registry

B-cell development and functions and therapeutic options in adenosine deaminase–deficient patients

Outcomes of MIS-C patients treated with anakinra: a retrospective multicenter national study

Discordance between Clinical and Ultrasound Examinations in Juvenile Idiopathic Arthritis: An Experimental Approach

Corrigendum: MIS-C Treatment: Is IVIG Always Necessary?

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