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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.
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.
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
Case Report: Interindividual variability and possible role of heterozygous variants in a family with deficiency of adenosine deaminase 2: are all heterozygous born equals?
Pulvirenti F, Cinicola BL, Ferrari S, Guadagnolo D, Sculco E, Capponi M, Loffredo L, Sciannamea M, Insalaco A, Quinti I, De Benedetti F, Zicari AM. Pulvirenti F, et al. Among authors: ferrari s. Front Immunol. 2023 May 3;14:1156689. doi: 10.3389/fimmu.2023.1156689. eCollection 2023. Front Immunol. 2023. PMID: 37207212 Free PMC article.
2,566 results