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Two X‐linked agammaglobulinemia patients develop pneumonia as COVID‐19 manifestation but recover

Pediatric allergy and immunology, 2020-07, Vol.31 (5), p.565-569

2020

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STAT mutations as program switchers: turning primary immunodeficiencies into autoimmune diseases

Journal of leukocyte biology, 2017-01, Vol.101 (1), p.29-38

2017

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Alternative Approach to Varicella Zoster Virus Prevention in a Child with Lymphopenia

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1681-1682

2021

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How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome

Blood, 2017-12, Vol.130 (23), p.2491-2498

2017

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Heightened Circulating Interferon-Inducible Chemokines, and Activated Pro-Cytolytic Th1-Cell Phenotype Features Covid-19 Aggravation in the Second Week of Illness

Frontiers in immunology, 2020-10, Vol.11, p.580987-580987

2020

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Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders

Current opinion in pediatrics, 2017-12, Vol.29 (6), p.711-717

2017

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The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)

Journal of clinical immunology, 2020-10, Vol.40 (7), p.1026-1037

2020

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Plasmacytoid Dendritic Cells Depletion and Elevation of IFN-γ Dependent Chemokines CXCL9 and CXCL10 in Children With Multisystem Inflammatory Syndrome

Frontiers in immunology, 2021-03, Vol.12, p.654587-654587

2021

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S180: RESULTS OF A PHASE 3 TRIAL OF AN ORAL CXCR4 ANTAGONIST, MAVORIXAFOR, FOR TREATMENT OF PATIENTS WITH WHIM SYNDROME

HemaSphere, 2023-08, Vol.7 (S3), p.e684700a-n/a

2023

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SARS-CoV-2 infection in cystic fibrosis: A multicentre prospective study with a control group, Italy, February-July 2020

PloS one, 2021-05, Vol.16 (5), p.e0251527-e0251527

2021

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Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1–mutated common variable immunodeficiency disease

Journal of allergy and clinical immunology, 2017-01, Vol.139 (1), p.349-352.e1

2017

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Successful Hematopoietic Stem Cell Transplantation in a Patient with Complete IFN-γ Receptor 2 Deficiency: a Case Report and Literature Review

Journal of clinical immunology, 2020-11, Vol.40 (8), p.1191-1195

2020

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Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations

Journal of allergy and clinical immunology, 2017-08, Vol.140 (2), p.553-564.e4

2017

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Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency

Journal of clinical immunology, 2017-10, Vol.37 (7), p.701-706

2017

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Bruton tyrosine kinase mediates TLR9 -dependent human dendritic cell activation

Journal of allergy and clinical immunology, 2014-06, Vol.133 (6), p.1644-1650.e4

2014

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Pathogenesis of Autoimmune Cytopenias in Inborn Errors of Immunity Revealing Novel Therapeutic Targets

Frontiers in immunology, 2022-04, Vol.13, p.846660-846660

2022

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Activin A as a mediator of NK-dendritic cell functional interactions

The Journal of immunology (1950), 2014-02, Vol.192 (3), p.1241-1248

2014

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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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Multisystem autoimmune disease caused by increased STAT3 phosphorylation and dysregulated gene expression

Haematologica (Roma), 2019-07, Vol.104 (7), p.e322-e325

2019

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Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation

Stem cell research, 2024-02, Vol.74, p.103293-103293, Article 103293

2024

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Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing

Frontiers in immunology, 2016-11, Vol.7, p.466-466

2016

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MicroRNA dysregulation in ataxia telangiectasia

Frontiers in immunology, 2024-08, Vol.15, p.1444130

2024

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Incidence of acute respiratory infections in preschool children in an outpatient setting before and during Covid-19 pandemic in Lombardy Region, Italy

Italian journal of pediatrics, 2022-02, Vol.48 (1), p.18-18, Article 18

2022

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Hermansky-Pudlak syndrome type II and lethal hemophagocytic lymphohistiocytosis: Case description and review of the literature

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-09, Vol.7 (7), p.2476-2478.e5

2019

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Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations

Journal of clinical immunology, 2022-02, Vol.42 (2), p.365-374

2022

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Two X‐linked agammaglobulinemia patients develop pneumonia as COVID‐19 manifestation but recover

STAT mutations as program switchers: turning primary immunodeficiencies into autoimmune diseases

Alternative Approach to Varicella Zoster Virus Prevention in a Child with Lymphopenia

How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome

Heightened Circulating Interferon-Inducible Chemokines, and Activated Pro-Cytolytic Th1-Cell Phenotype Features Covid-19 Aggravation in the Second Week of Illness

Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders

The Italian Registry for Primary Immunodeficiencies (Italian Primary Immunodeficiency Network; IPINet): Twenty Years of Experience (1999–2019)

Plasmacytoid Dendritic Cells Depletion and Elevation of IFN-γ Dependent Chemokines CXCL9 and CXCL10 in Children With Multisystem Inflammatory Syndrome

S180: RESULTS OF A PHASE 3 TRIAL OF AN ORAL CXCR4 ANTAGONIST, MAVORIXAFOR, FOR TREATMENT OF PATIENTS WITH WHIM SYNDROME

SARS-CoV-2 infection in cystic fibrosis: A multicentre prospective study with a control group, Italy, February-July 2020

Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1–mutated common variable immunodeficiency disease

Successful Hematopoietic Stem Cell Transplantation in a Patient with Complete IFN-γ Receptor 2 Deficiency: a Case Report and Literature Review

Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations

Long-Term Survival After Hematopoietic Stem Cell Transplantation for Complete STAT1 Deficiency

Bruton tyrosine kinase mediates TLR9 -dependent human dendritic cell activation

Pathogenesis of Autoimmune Cytopenias in Inborn Errors of Immunity Revealing Novel Therapeutic Targets

Activin A as a mediator of NK-dendritic cell functional interactions

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

Multisystem autoimmune disease caused by increased STAT3 phosphorylation and dysregulated gene expression

Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing

MicroRNA dysregulation in ataxia telangiectasia

Incidence of acute respiratory infections in preschool children in an outpatient setting before and during Covid-19 pandemic in Lombardy Region, Italy

Hermansky-Pudlak syndrome type II and lethal hemophagocytic lymphohistiocytosis: Case description and review of the literature

Immunological Evaluation of Patients Affected with Jacobsen Syndrome Reveals Profound Not Age-Related Lymphocyte Alterations

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