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Genes|January 28, 2026
Gene Panel Approach to Screen for Hereditary Cerebral Small Vessel Disease: A Proof-of-Concept StudyChiara Ferraro, Silvia Giliani, Alessandro PezziniCurrent Opinion in Allergy and Clinical Immunology|November 4, 2008
Cartilage-hair hypoplasia: molecular basis and heterogeneity of the immunological phenotypeLuigi D Notarangelo, Chaim M Roifman, Silvia GilianiCurrent Opinion in Allergy and Clinical Immunology|November 3, 2005
Cytokine-mediated signalling and early defects in lymphoid developmentSilvia Giliani, Patrizia Mella, Gianfranco Savoldi, et al.Immunologic Research|October 6, 2007
Immunodeficiencies due to defects of class-switch recombinationLuigi D Notarangelo, Gaetana Lanzi, Paola Toniati, et al.Reviews in Clinical and Experimental Hematology|December 25, 2003
Primary immune deficiencies unravel the molecular basis of immune responseLuigi D Notarangelo, Silvia Giliani, Evelina Mazzolari, et al.Journal of Clinical Immunology|July 7, 2011
Severe combined immunodeficiency in Greek children over a 20-year period: rarity of γc-chain deficiency (X-linked) typeAthanasios Michos, Marianna Tzanoudaki, Anna Villa, et al.Frontiers in Pediatrics|October 18, 2018
Heterozygous Mutation in Adenosine Deaminase Gene in a Patient With Severe Lymphopenia Following Corticosteroid Treatment of Autoimmune Hemolytic AnemiaSerena I Tripodi, Paola Corti, Silvia Giliani, et al.Pediatrics|December 10, 2021
Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two SiblingsLara Valeri, Licia Lugli, Lorenzo Iughetti, et al.Materials (Basel, Switzerland)|December 10, 2020
Selective Laser Melting and Electron Beam Melting of Ti6Al4V for Orthopedic Applications: A Comparative Study on the Applied Building DirectionPaola Ginestra, Rosalba Monica Ferraro, Keren Zohar-Hauber, et al.Expert Review of Clinical Immunology|May 19, 2010
The Wiskott-Aldrich syndrome: from genotype-phenotype correlation to treatmentDaniele Moratto, Silvia Giliani, Lucia D Notarangelo, et al.Pageof 10