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The Journal of Allergy and Clinical Immunology|July 6, 2014
A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiencyHassan Abolhassani, Ning Wang, Asghar Aghamohammadi, et al.Immunological Reviews|December 20, 2018
RAG gene defects at the verge of immunodeficiency and immune dysregulationAnna Villa, Luigi D NotarangeloActa Bio-Medica : Atenei Parmensis|November 11, 2011
Severe combined immunodeficiency (SCID): from molecular basis to clinical managementIvonne Sponzilli, Luigi D NotarangeloJournal of Leukocyte Biology|December 18, 2008
Leukocyte trafficking in primary immunodeficienciesLuigi D Notarangelo, Raffaele BadolatoThe Journal of Experimental Medicine|November 19, 2008
Out of breath: GM-CSFRalpha mutations disrupt surfactant homeostasisLuigi D Notarangelo, Itai PessachThe Journal of Allergy and Clinical Immunology|November 11, 2008
Is it necessary to identify molecular defects in primary immunodeficiency disease?Luigi D Notarangelo, Ricardo SorensenInternational Immunopharmacology|April 29, 2006
Therapeutic targeting of pattern-recognition receptorsNima RezaeiImmunity|November 9, 2022
Interferons in Down syndrome: When more is lessLuigi D Notarangelo, Marita BosticardoNature Reviews. Immunology|October 26, 2007
Immunological and genetic bases of new primary immunodeficienciesLászló Maródi, Luigi D NotarangeloSeminars in Immunology|March 2, 2023
Human thymus in health and disease: Recent advances in diagnosis and biologyMarita Bosticardo, Luigi D NotarangeloPageof 155