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The Journal of Allergy and Clinical Immunology. in Practice|March 30, 2019
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion SyndromeDavide Montin, Agostina Marolda, Francesco Licciardi, et al.
Frontiers in Medicine|July 26, 2021
Biotechnological Agents for Patients With Tumor Necrosis Factor Receptor Associated Periodic Syndrome-Therapeutic Outcome and Predictors of Response: Real-Life Data From the AIDA NetworkAntonio Vitale, Laura Obici, Marco Cattalini, et al.
Rheumatology (Oxford, England)|August 30, 2023
Early anakinra treatment improves cardiac outcome of multisystem inflammatory syndrome in children, regardless of disease severityAndrea Taddio, Sara Della Paolera, Luisa Abbagnato, et al.
Rheumatology (Oxford, England)|August 3, 2021
Canakinumab in systemic juvenile idiopathic arthritis: real-world data from a retrospective Italian cohortArianna De Matteis, Claudia Bracaglia, Denise Pires Marafon, et al.
The Journal of Allergy and Clinical Immunology|August 23, 2020
Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunityEmilia Cirillo, Giuliana Giardino, Silvia Ricci, et al.
Science Immunology|June 19, 2021
Heterozygous <i>OAS1</i> gain-of-function variants cause an autoinflammatory immunodeficiencyThomas Magg, Tsubasa Okano, Lars M Koenig, et al.
Frontiers in Immunology|August 29, 2019
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency NetworkEmilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
Eclinicalmedicine|March 11, 2026
Predictive value for intravenous immunoglobulin resistance of Kobayashi and Kawanet scores in 722 children with Kawasaki disease across diverse ethnic backgrounds (KIWI study): an international cohort studyMaria Vincenza Mastrolia, Vignesh Pandiarajan, Marco Cattalini, et al.
The Journal of Allergy and Clinical Immunology|July 9, 2013
Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresiasRui Chen, Silvia Giliani, Gaetana Lanzi, et al.
Mediators of Inflammation|August 25, 2020
Clinical Features at Onset and Genetic Characterization of Pediatric and Adult Patients with TNF-<i>α</i> Receptor-Associated Periodic Syndrome (TRAPS): A Series of 80 Cases from the AIDA NetworkCarla Gaggiano, Antonio Vitale, Laura Obici, et al.
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