Area of research
Immunology · Genetics
Research interest
Research interests include Medicine, Immunology, Biology, Primary immunodeficiency, Immune system, and Encephalitis.
Autoantibodies neutralizing type I IFNs in 40% of patients with WNV encephalitis in seven new cohorts
Early‐Life Heat Stress Impairs Cognition and Alters Its Covariation With Behaviour in Zebrafish
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease
Report of the Italian Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome in the Target Therapy Era
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation
An Automated Low-Cost Solution for Creating a Multiple-Step Thermal Gradient to Record Daily Fish Thermoregulatory Behavior
Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)
Clinical outcome, incidence, and SARS-CoV-2 infection-fatality rates in Italian patients with inborn errors of immunity
Neonatal Manifestations of Chronic Granulomatous Disease: MAS/HLH and Necrotizing Pneumonia as Unusual Phenotypes and Review of the Literature
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality
Expanding Phenotype of Schimke Immuno-Osseous Dysplasia: Congenital Anomalies of the Kidneys and of the Urinary Tract and Alteration of NK Cells
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
A 23-Year Follow-Up of a Patient with Gain-of-Function IkB-Alpha Mutation and Stable Full Chimerism After Hematopoietic Stem Cell Transplantation
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry
Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
Role of quercetin (a natural herbal compound) in allergy and inflammation.
PubMed 2016cited by 102position: middle
Mycobacterium simiae Infection in Two Unrelated Patients with Different Forms of Inherited IFN-γR2 Deficiency
Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency
Vascular Endothelial Growth Factor (VEGF), Mast Cells and Inflammation
IL-36 Receptor Antagonist with Special Emphasis on IL-38