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Blood|August 13, 2010
Different molecular behavior of CD40 mutants causing hyper-IgM syndromeGaetana Lanzi, Simona Ferrari, Mauno Vihinen, et al.
The Journal of Allergy and Clinical Immunology|March 8, 2011
A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP bindingMichel J Massaad, Narayanaswamy Ramesh, Severine Le Bras, et al.
Stem Cell Research|September 20, 2019
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Crohn's diseaseGaetana Lanzi, Stefania Masneri, Rosalba Monica Ferraro, et al.
Gels (Basel, Switzerland)|April 25, 2025
Three-Dimensional-Bioprinted Embedded-Based Cerebral Organoids: An Alternative Approach for Mini-Brain In Vitro Modeling Beyond Conventional Generation MethodsRosalba Monica Ferraro, Paola Serena Ginestra, Miriam Seiti, et al.
Frontiers in Pediatrics|November 15, 2021
Case Report: The JAK-Inhibitor Ruxolitinib Use in Aicardi-Goutieres Syndrome Due to ADAR1 MutationMarco Cattalini, Jessica Galli, Fiammetta Zunica, et al.
Frontiers in Immunology|July 18, 2020
Transient Decrease of Circulating and Tissular Dendritic Cells in Patients With Mycobacterial Disease and With Partial Dominant IFNγR1 DeficiencyLaura Dotta, Donatella Vairo, Mauro Giacomelli, et al.
Le Infezioni in Medicina|March 19, 2019
Pseudomonas aeruginosa severe skin infection in a toddler with X-linked agammaglobulinemia due to a novel BTK mutationNiccoló Riccardi, Gioacchino Andrea Rotulo, Federica Favilli, et al.
The Journal of Pediatrics|February 24, 2006
Omenn syndrome in an infant with IL7RA gene mutationSilvia Giliani, Carmen Bonfim, Genevieve de Saint Basile, et al.
Blood|March 6, 2002
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopeniaLucia D Notarangelo, Cinzia Mazza, Silvia Giliani, et al.
Blood|July 21, 2011
Severe impairment of IFN-γ and IFN-α responses in cells of a patient with a novel STAT1 splicing mutationDonatella Vairo, Laura Tassone, Giovanna Tabellini, et al.
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