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Page 1
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: facchetti f. 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.
AIRE deficiency in thymus of 2 patients with Omenn syndrome.
Cavadini P, Vermi W, Facchetti F, Fontana S, Nagafuchi S, Mazzolari E, Sediva A, Marrella V, Villa A, Fischer A, Notarangelo LD, Badolato R. Cavadini P, et al. Among authors: facchetti f. J Clin Invest. 2005 Mar;115(3):728-32. doi: 10.1172/JCI23087. J Clin Invest. 2005. PMID: 15696198 Free PMC article.
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
Innate immunity defects in Hermansky-Pudlak type 2 syndrome.
Fontana S, Parolini S, Vermi W, Booth S, Gallo F, Donini M, Benassi M, Gentili F, Ferrari D, Notarangelo LD, Cavadini P, Marcenaro E, Dusi S, Cassatella M, Facchetti F, Griffiths GM, Moretta A, Notarangelo LD, Badolato R. Fontana S, et al. Among authors: facchetti f. Blood. 2006 Jun 15;107(12):4857-64. doi: 10.1182/blood-2005-11-4398. Epub 2006 Feb 28. Blood. 2006. PMID: 16507770 Free article.
G-CSF treatment of severe congenital neutropenia reverses neutropenia but does not correct the underlying functional deficiency of the neutrophil in defending against microorganisms.
Donini M, Fontana S, Savoldi G, Vermi W, Tassone L, Gentili F, Zenaro E, Ferrari D, Notarangelo LD, Porta F, Facchetti F, Notarangelo LD, Dusi S, Badolato R. Donini M, et al. Among authors: facchetti f. Blood. 2007 Jun 1;109(11):4716-23. doi: 10.1182/blood-2006-09-045427. Epub 2007 Feb 20. Blood. 2007. PMID: 17311988 Free article.
A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome.
Marrella V, Poliani PL, Casati A, Rucci F, Frascoli L, Gougeon ML, Lemercier B, Bosticardo M, Ravanini M, Battaglia M, Roncarolo MG, Cavazzana-Calvo M, Facchetti F, Notarangelo LD, Vezzoni P, Grassi F, Villa A. Marrella V, et al. Among authors: facchetti f. J Clin Invest. 2007 May;117(5):1260-9. doi: 10.1172/JCI30928. J Clin Invest. 2007. PMID: 17476358 Free PMC article.
468 results