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The Journal of Allergy and Clinical Immunology|April 21, 2020
Cutaneous barrier leakage and gut inflammation drive skin disease in Omenn syndromeRosita Rigoni, Elena Fontana, Kerry Dobbs, et al.
Frontiers in Immunology|June 20, 2019
Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary ImmunodeficienciesCristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Science Translational Medicine|February 7, 2024
Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiencyMaria Carmina Castiello, Chiara Brandas, Samuele Ferrari, et al.
Frontiers in Immunology|April 30, 2019
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary ImmunodeficienciesCristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Science (New York, N.Y.)|July 13, 2013
Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndromeAlessandro Aiuti, Luca Biasco, Samantha Scaramuzza, et al.
The Lancet. Haematology|April 15, 2019
Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical studyFrancesca Ferrua, Maria Pia Cicalese, Stefania Galimberti, et al.
Blood|September 27, 2018
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiencyImmacolata Brigida, Matteo Zoccolillo, Maria Pia Cicalese, et al.
The Journal of Experimental Medicine|May 2, 2025
Immunopathological and microbial signatures of inflammatory bowel disease in partial RAG deficiencyRiccardo Castagnoli, Francesca Pala, Poorani Subramanian, et al.
Science Immunology|January 10, 2025
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signatureMarita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, et al.
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