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Page 1
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease.
Dotta L, Scomodon O, Padoan R, Timpano S, Plebani A, Soresina A, Lougaris V, Concolino D, Nicoletti A, Giardino G, Licari A, Marseglia G, Pignata C, Tamassia N, Facchetti F, Vairo D, Badolato R. Dotta L, et al. Among authors: facchetti f. Clin Immunol. 2016 Mar;164:1-9. doi: 10.1016/j.clim.2015.12.010. Epub 2015 Dec 28. Clin Immunol. 2016. PMID: 26732859
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease.
Dotta L, Scomodon O, Padoan R, Timpano S, Plebani A, Soresina A, Lougaris V, Concolino D, Nicoletti A, Giardino G, Licari A, Marseglia G, Pignata C, Tamassia N, Facchetti F, Vairo D, Badolato R. Dotta L, et al. Among authors: facchetti f. Data Brief. 2016 Feb 23;7:311-5. doi: 10.1016/j.dib.2016.02.040. eCollection 2016 Jun. Data Brief. 2016. PMID: 26981552 Free PMC article.
Paediatric MAS/HLH caused by a novel monoallelic activating mutation in p110δ.
Lougaris V, Baronio M, Castagna A, Tessarin G, Rossi S, Gazzurelli L, Benvenuto A, Moratto D, Chiarini M, Cattalini M, Facchetti M, Palumbo L, Giliani S, Girelli MF, Badolato R, Bondioni MP, Facchetti F, Meini A, Plebani A. Lougaris V, et al. Among authors: facchetti m, facchetti f. Clin Immunol. 2020 Oct;219:108543. doi: 10.1016/j.clim.2020.108543. Epub 2020 Jul 16. Clin Immunol. 2020. PMID: 32681977
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype.
Lougaris V, Faletra F, Lanzi G, Vozzi D, Marcuzzi A, Valencic E, Piscianz E, Bianco A, Girardelli M, Baronio M, Loganes C, Fasth A, Salvini F, Trizzino A, Moratto D, Facchetti F, Giliani S, Plebani A, Tommasini A. Lougaris V, et al. Among authors: facchetti f. Clin Immunol. 2015 Jul;159(1):33-6. doi: 10.1016/j.clim.2015.04.014. Epub 2015 May 1. Clin Immunol. 2015. PMID: 25939554 No abstract available.
Defect of regulatory T cells in patients with Omenn syndrome.
Cassani B, Poliani PL, Moratto D, Sobacchi C, Marrella V, Imperatori L, Vairo D, Plebani A, Giliani S, Vezzoni P, Facchetti F, Porta F, Notarangelo LD, Villa A, Badolato R. Cassani B, et al. Among authors: facchetti f. J Allergy Clin Immunol. 2010 Jan;125(1):209-16. doi: 10.1016/j.jaci.2009.10.023. J Allergy Clin Immunol. 2010. PMID: 20109747
Acral lympho-histiocytic dermatitis in X-linked agammaglobulinemia: a case report showing clonal CD8(+) T cells with indolent clinical behaviour.
Gualdi G, Lorenzi L, Arisi M, Maffeis M, Soresina A, Marocolo D, Plebani A, Calzavara-Pinton PG, Facchetti F. Gualdi G, et al. Among authors: facchetti f. J Eur Acad Dermatol Venereol. 2016 Mar;30(3):461-3. doi: 10.1111/jdv.12839. Epub 2014 Nov 11. J Eur Acad Dermatol Venereol. 2016. PMID: 25388899 No abstract available.
Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis.
Galli J, Gavazzi F, De Simone M, Giliani S, Garau J, Valente M, Vairo D, Cattalini M, Mortilla M, Andreoli L, Badolato R, Bianchi M, Carabellese N, Cereda C, Ferraro R, Facchetti F, Fredi M, Gualdi G, Lorenzi L, Meini A, Orcesi S, Tincani A, Zanola A, Rice G, Fazzi E; AGS study group. Galli J, et al. Among authors: facchetti f. Medicine (Baltimore). 2018 Dec;97(52):e13893. doi: 10.1097/MD.0000000000013893. Medicine (Baltimore). 2018. PMID: 30593198 Free PMC article.
Type I interferon-dependent gene MxA in perinatal HIV-infected patients under antiretroviral therapy as marker for therapy failure and blood plasmacytoid dendritic cells depletion.
Badolato R, Ghidini C, Facchetti F, Serana F, Sottini A, Chiarini M, Spinelli E, Lonardi S, Plebani A, Caimi L, Imberti L. Badolato R, et al. Among authors: facchetti f. J Transl Med. 2008 Sep 9;6:49. doi: 10.1186/1479-5876-6-49. J Transl Med. 2008. PMID: 18782441 Free PMC article.
468 results