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Page 1
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.
Cagliani R, Fumagalli M, Guerini FR, Riva S, Galimberti D, Comi GP, Agliardi C, Scarpini E, Pozzoli U, Forni D, Caputo D, Asselta R, Biasin M, Paraboschi EM, Bresolin N, Clerici M, Sironi M. Cagliani R, et al. Among authors: agliardi c. Hum Genet. 2012 Jan;131(1):87-97. doi: 10.1007/s00439-011-1053-2. Epub 2011 Jul 7. Hum Genet. 2012. PMID: 21735172 Free PMC article.
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy.
D'Alfonso S, Bolognesi E, Guerini FR, Barizzone N, Bocca S, Ferrante D, Castelli L, Bergamaschi L, Agliardi C, Ferrante P, Naldi P, Leone M, Caputo D, Ballerini C, Salvetti M, Galimberti D, Massacesi L, Trojano M, Momigliano-Richiardi P. D'Alfonso S, et al. Among authors: agliardi c. Genes Immun. 2008 Jan;9(1):7-15. doi: 10.1038/sj.gene.6364437. Epub 2007 Oct 11. Genes Immun. 2008. PMID: 17928868
HLA-Cw allele frequencies in northern and southern Italy.
Guerini FR, Fusco C, Mazzi B, Favoino B, Nocera G, Agliardi C, Ceresa D, Valentino M, Mininni D, Zanzottera M, Ferrante P, Lombardi ML. Guerini FR, et al. Among authors: agliardi c. Transpl Immunol. 2008 Jan;18(3):286-9. doi: 10.1016/j.trim.2007.08.003. Epub 2007 Aug 27. Transpl Immunol. 2008. PMID: 18047939
Association study of the HLA-A2 allele in Italian Alzheimer disease patients.
Guerini FR, Calabrese E, Agliardi C, Zanzottera M, Franceschi M, Grimaldi LM, Nemni R, Ferrante P. Guerini FR, et al. Among authors: agliardi c. Neurobiol Aging. 2009 Dec;30(12):2082-3. doi: 10.1016/j.neurobiolaging.2008.02.001. Epub 2008 Mar 21. Neurobiol Aging. 2009. PMID: 18359130
HLA-DRB1 polymorphisms distribution in chronic dysimmune polyneuropathy.
Gironi M, Guerini FR, Beghi E, Antonini G, Martinelli-Boneschi F, Ceresa L, Morino S, Agliardi C, Ferrante P, Nemni R. Gironi M, et al. Among authors: agliardi c. Neuromuscul Disord. 2008 Dec;18(12):967-9. doi: 10.1016/j.nmd.2008.07.008. Epub 2008 Sep 11. Neuromuscul Disord. 2008. PMID: 18789688
73 results