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Page 1
Working the endless puzzle of hereditary autoinflammatory disorders.
Caso F, Cantarini L, Lucherini OM, Sfriso P, Fioretti M, Costa L, Vitale A, Atteno M, Galeazzi M, Muscari I, Magnotti F, Frediani B, Punzi L, Rigante D. Caso F, et al. Among authors: magnotti f. Mod Rheumatol. 2014 May;24(3):381-9. doi: 10.3109/14397595.2013.843755. Epub 2013 Oct 18. Mod Rheumatol. 2014. PMID: 24251993 Review.
The labyrinth of autoinflammatory disorders: a snapshot on the activity of a third-level center in Italy.
Cantarini L, Vitale A, Lucherini OM, De Clemente C, Caso F, Costa L, Emmi G, Silvestri E, Magnotti F, Maggio MC, Prinzi E, Lopalco G, Frediani B, Cimaz R, Galeazzi M, Rigante D. Cantarini L, et al. Among authors: magnotti f. Clin Rheumatol. 2015 Jan;34(1):17-28. doi: 10.1007/s10067-014-2721-0. Epub 2014 Jun 24. Clin Rheumatol. 2015. PMID: 24953660 Review.
Weekly oral alendronate in mevalonate kinase deficiency.
Cantarini L, Vitale A, Magnotti F, Lucherini OM, Caso F, Frediani B, Galeazzi M, Rigante D. Cantarini L, et al. Among authors: magnotti f. Orphanet J Rare Dis. 2013 Dec 20;8:196. doi: 10.1186/1750-1172-8-196. Orphanet J Rare Dis. 2013. PMID: 24360083 Free PMC article.
Differential impact of high and low penetrance TNFRSF1A gene mutations on conventional and regulatory CD4+ T cell functions in TNFR1-associated periodic syndrome.
Pucino V, Lucherini OM, Perna F, Obici L, Merlini G, Cattalini M, La Torre F, Maggio MC, Lepore MT, Magnotti F, Galgani M, Galeazzi M, Marone G, De Rosa V, Talarico R, Cantarini L, Matarese G. Pucino V, et al. Among authors: magnotti f. J Leukoc Biol. 2016 May;99(5):761-9. doi: 10.1189/jlb.3A0915-399R. Epub 2015 Nov 23. J Leukoc Biol. 2016. PMID: 26598380
Immunometabolic biomarkers of inflammation in Behçet's disease: relationship with epidemiological profile, disease activity and therapeutic regimens.
Cantarini L, Pucino V, Vitale A, Talarico R, Lucherini OM, Magnotti F, De Rosa V, Galgani M, Alviggi C, Marone G, Galeazzi M, Matarese G. Cantarini L, et al. Among authors: magnotti f. Clin Exp Immunol. 2016 May;184(2):197-207. doi: 10.1111/cei.12768. Epub 2016 Feb 24. Clin Exp Immunol. 2016. PMID: 26756979 Free PMC article.
Familial Mediterranean fever mutations are hypermorphic mutations that specifically decrease the activation threshold of the Pyrin inflammasome.
Jamilloux Y, Lefeuvre L, Magnotti F, Martin A, Benezech S, Allatif O, Penel-Page M, Hentgen V, Sève P, Gerfaud-Valentin M, Duquesne A, Desjonquères M, Laurent A, Rémy-Piccolo V, Cimaz R, Cantarini L, Bourdonnay E, Walzer T, Py BF, Belot A, Henry T. Jamilloux Y, et al. Among authors: magnotti f. Rheumatology (Oxford). 2018 Jan 1;57(1):100-111. doi: 10.1093/rheumatology/kex373. Rheumatology (Oxford). 2018. PMID: 29040788
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