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Weaving Mitochondrial DNA and Y-Chromosome Variation in the Panamanian Genetic Canvas.
Rambaldi Migliore N, Colombo G, Capodiferro MR, Mazzocchi L, Chero Osorio AM, Raveane A, Tribaldos M, Perego UA, Mendizábal T, Montón AG, Lombardo G, Grugni V, Garofalo M, Ferretti L, Cereda C, Gagliardi S, Cooke R, Smith-Guzmán N, Olivieri A, Aram B, Torroni A, Motta J, Semino O, Achilli A. Rambaldi Migliore N, et al. Among authors: gagliardi s. Genes (Basel). 2021 Nov 29;12(12):1921. doi: 10.3390/genes12121921. Genes (Basel). 2021. PMID: 34946870 Free PMC article.
SOD1 mRNA expression in sporadic amyotrophic lateral sclerosis.
Gagliardi S, Cova E, Davin A, Guareschi S, Abel K, Alvisi E, Laforenza U, Ghidoni R, Cashman JR, Ceroni M, Cereda C. Gagliardi S, et al. Neurobiol Dis. 2010 Aug;39(2):198-203. doi: 10.1016/j.nbd.2010.04.008. Epub 2010 Apr 23. Neurobiol Dis. 2010. PMID: 20399857
Legius Syndrome: two novel mutations in the SPRED1 gene.
Bianchi M, Saletti V, Micheli R, Esposito S, Molinaro A, Gagliardi S, Orcesi S, Cereda C. Bianchi M, et al. Among authors: gagliardi s. Hum Genome Var. 2015 Dec 3;2:15051. doi: 10.1038/hgv.2015.51. eCollection 2015. Hum Genome Var. 2015. PMID: 27081556 Free PMC article.
Palmoplantar keratoderma and Charcot-Marie-Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole-exome sequencing.
Gagliardi S, Ricca I, Ferrarini A, Valente M, Grieco GS, Piccolo G, Alfonsi E, Delledonne M, Cereda C. Gagliardi S, et al. Br J Dermatol. 2017 Jul;177(1):284-286. doi: 10.1111/bjd.15066. Epub 2017 Jun 14. Br J Dermatol. 2017. PMID: 27639257 No abstract available.
232 results