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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1984 1
1989 2
1993 1
1994 1
1997 1
1998 1
1999 1
2000 2
2003 2
2005 1
2006 1
2008 2
2009 1
2011 1
2012 1
2014 3
2015 1
2016 2
2018 4
2019 3
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2022 1
2023 1
2024 0

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34 results

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Page 1
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.
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. Among authors: specchia fg. 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.
Evolution of hypogammaglobulinemia in premature and full-term infants.
Ricci G, Piccinno V, Giannetti A, Miniaci A, Specchia F, Masi M. Ricci G, et al. Among authors: specchia f. Int J Immunopathol Pharmacol. 2011 Jul-Sep;24(3):721-6. doi: 10.1177/039463201102400318. Int J Immunopathol Pharmacol. 2011. PMID: 21978704 Free article.
Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
Cancrini C, Puliafito P, Digilio MC, Soresina A, Martino S, Rondelli R, Consolini R, Ruga EM, Cardinale F, Finocchi A, Romiti ML, Martire B, Bacchetta R, Albano V, Carotti A, Specchia F, Montin D, Cirillo E, Cocchi G, Trizzino A, Bossi G, Milanesi O, Azzari C, Corsello G, Pignata C, Aiuti A, Pietrogrande MC, Marino B, Ugazio AG, Plebani A, Rossi P; Italian Network for Primary Immunodeficiencies. Cancrini C, et al. Among authors: specchia f. J Pediatr. 2014 Jun;164(6):1475-80.e2. doi: 10.1016/j.jpeds.2014.01.056. Epub 2014 Mar 20. J Pediatr. 2014. PMID: 24657119
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
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.
34 results