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Page 1
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study.
Dellepiane RM, Dell'Era L, Beilis LV, Pavesi P, Raimondi M, Soresina A, Lougaris V, Carrabba M, Martire B, Martino S, Russo G, Patuzzo G, Pignata C, Spadaro G, Gallizzi R, Duse M, Specchia FG, Moschese V, Marseglia GL, Pietrogrande MC, Bedogni G, Agostoni C. Dellepiane RM, et al. J Clin Immunol. 2015 Oct;35(7):595-7. doi: 10.1007/s10875-015-0195-8. Epub 2015 Sep 18. J Clin Immunol. 2015. PMID: 26384979 No abstract available.
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome.
Lougaris V, Facchini E, Baronio M, Lorenzini T, Moratto D, Specchia F, Plebani A. Lougaris V, et al. Among authors: specchia f. Clin Immunol. 2016 Dec;173:181-183. doi: 10.1016/j.clim.2016.10.019. Epub 2016 Nov 5. Clin Immunol. 2016. PMID: 27825976 No abstract available.
Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind study.
Cirillo E, Del Giudice E, Micheli R, Cappellari AM, Soresina A, Dellepiane RM, Pietrogrande MC, Dell'Era L, Specchia F, Pession A, Plebani A, Pignata C. Cirillo E, et al. Among authors: specchia f. Eur J Neurol. 2018 Jun;25(6):833-840. doi: 10.1111/ene.13606. Epub 2018 Mar 26. Eur J Neurol. 2018. PMID: 29489040
Follow-up and outcome of symptomatic partial or absolute IgA deficiency in children.
Moschese V, Chini L, Graziani S, Sgrulletti M, Gallo V, Di Matteo G, Ferrari S, Di Cesare S, Cirillo E, Pession A, Pignata C, Specchia F. Moschese V, et al. Among authors: specchia f. Eur J Pediatr. 2019 Jan;178(1):51-60. doi: 10.1007/s00431-018-3248-1. Epub 2018 Sep 29. Eur J Pediatr. 2019. PMID: 30269248
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network.
Cirillo E, Cancrini C, Azzari C, Martino S, Martire B, Pession A, Tommasini A, Naviglio S, Finocchi A, Consolini R, Pierani P, D'Alba I, Putti MC, Marzollo A, Giardino G, Prencipe R, Esposito F, Grasso F, Scarselli A, Di Matteo G, Attardi E, Ricci S, Montin D, Specchia F, Barzaghi F, Cicalese MP, Quaremba G, Lougaris V, Giliani S, Locatelli F, Rossi P, Aiuti A, Badolato R, Plebani A, Pignata C. Cirillo E, et al. Among authors: specchia f. Front Immunol. 2019 Aug 13;10:1908. doi: 10.3389/fimmu.2019.01908. eCollection 2019. Front Immunol. 2019. PMID: 31456805 Free PMC article.
Follicular helper T cell signature of replicative exhaustion, apoptosis, and senescence in common variable immunodeficiency.
Milardi G, Di Lorenzo B, Gerosa J, Barzaghi F, Di Matteo G, Omrani M, Jofra T, Merelli I, Barcella M, Filippini M, Conti A, Ferrua F, Pozzo Giuffrida F, Dionisio F, Rovere-Querini P, Marktel S, Assanelli A, Piemontese S, Brigida I, Zoccolillo M, Cirillo E, Giardino G, Danieli MG, Specchia F, Pacillo L, Di Cesare S, Giancotta C, Romano F, Matarese A, Chetta AA, Trimarchi M, Laurenzi A, De Pellegrin M, Darin S, Montin D, Marinoni M, Dellepiane RM, Sordi V, Lougaris V, Vacca A, Melzi R, Nano R, Azzari C, Bongiovanni L, Pignata C, Cancrini C, Plebani A, Piemonti L, Petrovas C, Di Micco R, Ponzoni M, Aiuti A, Cicalese MP, Fousteri G. Milardi G, et al. Among authors: specchia f. Eur J Immunol. 2022 Jul;52(7):1171-1189. doi: 10.1002/eji.202149480. Epub 2022 May 29. Eur J Immunol. 2022. PMID: 35562849 Free PMC article.
Autosomal-dominant hyper-IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: Evidence from the Italian cohort of 61 patients with elevated IgE.
Lorenzini T, Giacomelli M, Scomodon O, Cortesi M, Rivellini V, Dotta L, Soresina A, Dellepiane RM, Carrabba M, Cossu F, Cancrini C, Specchia F, Giardino G, Pignata C, Plebani A, Pietrogrande MC, Badolato R; IPINET (Italian Network for Primary Immunodeficiencies). Lorenzini T, et al. Among authors: specchia f. J Allergy Clin Immunol Pract. 2019 Jul-Aug;7(6):2072-2075.e4. doi: 10.1016/j.jaip.2019.02.012. Epub 2019 Feb 20. J Allergy Clin Immunol Pract. 2019. PMID: 30797078 No abstract available.
36 results