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Page 1
Anhidrotic ectodermal dysplasia: a new mutation.
Giancane G, Ferrari S, Carsetti R, Papoff P, Iacobini M, Duse M. Giancane G, et al. Among authors: ferrari s. J Allergy Clin Immunol. 2013 Dec;132(6):1451-3. doi: 10.1016/j.jaci.2013.05.034. Epub 2013 Jul 16. J Allergy Clin Immunol. 2013. PMID: 23870671 No abstract available.
Functional defects of dendritic cells in patients with CD40 deficiency.
Fontana S, Moratto D, Mangal S, De Francesco M, Vermi W, Ferrari S, Facchetti F, Kutukculer N, Fiorini C, Duse M, Das PK, Notarangelo LD, Plebani A, Badolato R. Fontana S, et al. Among authors: ferrari s. Blood. 2003 Dec 1;102(12):4099-106. doi: 10.1182/blood-2003-04-1244. Epub 2003 Jul 31. Blood. 2003. PMID: 12893749 Free article.
Ig beta deficiency in humans.
Lougaris V, Ferrari S, Plebani A. Lougaris V, et al. Among authors: ferrari s. Curr Opin Allergy Clin Immunol. 2008 Dec;8(6):515-9. doi: 10.1097/ACI.0b013e328314b621. Curr Opin Allergy Clin Immunol. 2008. PMID: 18978465 Review.
Rare TACI Mutation in a 3-Year-Old Boy With CVID Phenotype.
Leonardi L, Lorenzetti G, Carsetti R, Ferrari S, Di Felice A, Cinicola B, Duse M. Leonardi L, et al. Among authors: ferrari s. Front Pediatr. 2019 Oct 15;7:418. doi: 10.3389/fped.2019.00418. eCollection 2019. Front Pediatr. 2019. PMID: 31681716 Free PMC article.
Long-term follow-up of 168 patients with X-linked agammaglobulinemia reveals increased morbidity and mortality.
Lougaris V, Soresina A, Baronio M, Montin D, Martino S, Signa S, Volpi S, Zecca M, Marinoni M, Baselli LA, Dellepiane RM, Carrabba M, Fabio G, Putti MC, Cinetto F, Lunardi C, Gazzurelli L, Benvenuto A, Bertolini P, Conti F, Consolini R, Ricci S, Azzari C, Leonardi L, Duse M, Pulvirenti F, Milito C, Quinti I, Cancrini C, Finocchi A, Moschese V, Cirillo E, Crescenzi L, Spadaro G, Marasco C, Vacca A, Cardinale F, Martire B, Trizzino A, Licciardello M, Cossu F, Di Matteo G, Badolato R, Ferrari S, Giliani S, Pession A, Ugazio A, Pignata C, Plebani A. Lougaris V, et al. Among authors: ferrari s. J Allergy Clin Immunol. 2020 Aug;146(2):429-437. doi: 10.1016/j.jaci.2020.03.001. Epub 2020 Mar 10. J Allergy Clin Immunol. 2020. PMID: 32169379
T-Cell Defects Associated to Lack of Spike-Specific Antibodies after BNT162b2 Full Immunization Followed by a Booster Dose in Patients with Common Variable Immune Deficiencies.
Pulvirenti F, Di Cecca S, Sinibaldi M, Piano Mortari E, Terreri S, Albano C, Guercio M, Sculco E, Milito C, Ferrari S, Locatelli F, Quintarelli C, Carsetti R, Quinti I. Pulvirenti F, et al. Among authors: ferrari s. Cells. 2022 Jun 14;11(12):1918. doi: 10.3390/cells11121918. Cells. 2022. PMID: 35741048 Free PMC article.
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for the diagnosis of inborn errors of immunity (IEI).
Giardino G, Di Matteo G, Giliani S, Ferrari S, Lougaris V, Badolato R, Conti F, Romano R, Cicalese MP, Ricci S, Barzaghi F, Marzollo A, Cifaldi C, Montin D, Lodi L, Cirillo E, Martire B, Trizzino A, Sgrulletti M, Moschese V, Comegna M, Castaldo G, Tommasini A, Azzari C, Cancrini C, Aiuti A, Pignata C. Giardino G, et al. Among authors: ferrari s. J Allergy Clin Immunol. 2024 Nov 30:S0091-6749(24)01282-X. doi: 10.1016/j.jaci.2024.11.030. Online ahead of print. J Allergy Clin Immunol. 2024. PMID: 39622296
2,632 results