| Humoral and cellular response following vaccination with the BNT162b2 mRNA COVID-19 vaccine in patients affected by primary immunodeficiencies D Amodio, A Ruggiero, M Sgrulletti, C Pighi, N Cotugno, C Medri, ... Frontiers in immunology 12, 727850, 2021 | 85 | 2021 |
| Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease M Sharma, D Leung, M Momenilandi, LCW Jones, L Pacillo, AE James, ... Journal of Experimental Medicine 220 (5), e20221755, 2023 | 49 | 2023 |
| Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency G Milardi, B Di Lorenzo, J Gerosa, F Barzaghi, G Di Matteo, M Omrani, ... European Journal of Immunology 52 (7), 1171-1189, 2022 | 14 | 2022 |
| Case report: EBV chronic infection and lymphoproliferation in four APDS patients: the challenge of proper characterization, therapy, and follow-up B Rivalta, D Amodio, C Milito, M Chiriaco, S Di Cesare, C Giancotta, ... Frontiers in Pediatrics 9, 703853, 2021 | 14 | 2021 |
| Activated phosphoinositide 3-kinase δ syndrome: update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity ME Maccari, M Wolkewitz, C Schwab, T Lorenzini, JW Leiding, N Aladjdi, ... Journal of Allergy and Clinical Immunology 152 (4), 984-996. e10, 2023 | 11 | 2023 |
| Urogenital abnormalities in adenosine deaminase deficiency R Pajno, L Pacillo, S Recupero, MP Cicalese, F Ferrua, F Barzaghi, ... Journal of clinical immunology 40, 610-618, 2020 | 8 | 2020 |
| Long term longitudinal follow-up of an AD-HIES cohort: the impact of early diagnosis and enrollment to IPINet centers on the natural history of Job’s syndrome M Carrabba, RM Dellepiane, M Cortesi, LA Baselli, A Soresina, E Cirillo, ... Allergy, Asthma & Clinical Immunology 19 (1), 32, 2023 | 5 | 2023 |
| Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait? M Chiriaco, GM Ursu, D Amodio, N Cotugno, S Volpi, F Berardinelli, ... Frontiers in Immunology 13, 919237, 2022 | 5 | 2022 |
| Clinical, immunological, and molecular variability of rag deficiency: a retrospective analysis of 22 rag patients C Cifaldi, B Rivalta, D Amodio, A Mattia, L Pacillo, S Di Cesare, ... Journal of Clinical Immunology, 1-16, 2021 | 5 | 2021 |
| In Search for the Missing Link in APECED-like Conditions: Analysis of the AIRE Gene in a Series of 48 Patients A Fierabracci, E Belcastro, E Carbone, O Pagliarosi, A Palma, L Pacillo, ... Journal of Clinical Medicine 11 (11), 3242, 2022 | 4 | 2022 |
| Immune tolerance breakdown in inborn errors of immunity: paving the way to novel therapeutic approaches G Giardino, R Romano, V Lougaris, R Castagnoli, F Cillo, L Leonardi, ... Clinical Immunology 251, 109302, 2023 | 3 | 2023 |
| Tailored treatments in inborn errors of immunity associated with atopy (IEIs-A) with skin involvement C Giancotta, N Colantoni, L Pacillo, V Santilli, D Amodio, EC Manno, ... Frontiers in Pediatrics 11, 1129249, 2023 | 3 | 2023 |
| Targeted treatment of autoimmune cytopenias in primary immunodeficiencies L Pacillo, G Giardino, D Amodio, C Giancotta, B Rivalta, GA Rotulo, ... Frontiers in Immunology 13, 911385, 2022 | 3 | 2022 |
| SARS‐CoV‐2 infection and treatment in a cohort of patients with inborn errors of immunity F Conti, L Pacillo, D Amodio, B Rivalta, M Moratti, C Campoli, D Zama, ... Pediatric Allergy and Immunology 33 (8), 2022 | 3 | 2022 |
| Case report: Successful treatment with monoclonal antibodies in one APDS patient with prolonged SARS-CoV-2 infection not responsive to previous lines of treatment B Rivalta, D Amodio, C Giancotta, V Santilli, L Pacillo, P Zangari, ... Frontiers in Immunology 13, 891274, 2022 | 3 | 2022 |
| Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report B Di Lorenzo, L Pacillo, G Milardi, T Jofra, S Di Cesare, J Gerosa, ... Frontiers in Immunology 13, 952715, 2022 | 2 | 2022 |
| Natural history of Ras-associated autoimmune leukoproliferative disorder: A 20-year follow-up of a NRAS-mutated patient excluding a malignant progression B Rivalta, E Attardi, C Cifaldi, V Rosti, L Pacillo, H Hajrullaj, S Di Cesare, ... British journal of haematology 204 (1), e6-e10, 2024 | 1 | 2024 |
| Case report: Neonatal-onset inflammatory bowel disease due to novel compound heterozygous mutations in DUOX2 A Finocchi, L Pacillo, M Chiriaco, G Di Matteo, P Francalanci, G Angelino, ... Frontiers in Genetics 14, 1276697, 2023 | 1 | 2023 |
| Risk of thyroid neoplasms in patients with 22q11. 2 deletion and DiGeorge-like syndromes: an insight for follow-up WM Sarli, S Ricci, L Lodi, F Cavone, L Pacillo, C Giancotta, G Ubertini, ... Frontiers in Endocrinology 14, 1209577, 2023 | 1 | 2023 |
| Clinical Features and Outcomes in STING-Associated Vasculopathy with Onset in Infancy (SAVI) S Torreggiani, S Alehashemi, J Mitchell, GS Adeva, B Lin, J Wade, ... ARTHRITIS & RHEUMATOLOGY 72, 2020 | 1 | 2020 |
