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Vascular Remodeling in Moyamoya Angiopathy: From Peripheral Blood Mononuclear Cells to Endothelial Cells.
Tinelli F, Nava S, Arioli F, Bedini G, Scelzo E, Lisini D, Faragò G, Gioppo A, Ciceri EF, Acerbi F, Ferroli P, Vetrano IG, Esposito S, Saletti V, Pantaleoni C, Zibordi F, Nardocci N, Zedde ML, Pezzini A, Di Lazzaro V, Capone F, Dell'Acqua ML, Vajkoczy P, Tournier-Lasserve E, Parati EA, Bersano A, Gatti L. Tinelli F, et al. Among authors: saletti v. Int J Mol Sci. 2020 Aug 11;21(16):5763. doi: 10.3390/ijms21165763. Int J Mol Sci. 2020. PMID: 32796702 Free PMC article.
Neurological pictures in paediatric Chiari I malformation.
Saletti V, Esposito S, Frittoli M, Valentini LG, Chiapparini L, Bulgheroni S, Riva D. Saletti V, et al. Neurol Sci. 2011 Dec;32 Suppl 3:S295-8. doi: 10.1007/s10072-011-0744-8. Neurol Sci. 2011. PMID: 21983864
126 novel mutations in Italian patients with neurofibromatosis type 1.
Bianchessi D, Morosini S, Saletti V, Ibba MC, Natacci F, Esposito S, Cesaretti C, Riva D, Finocchiaro G, Eoli M. Bianchessi D, et al. Among authors: saletti v. Mol Genet Genomic Med. 2015 Jul 7;3(6):513-25. doi: 10.1002/mgg3.161. eCollection 2015 Nov. Mol Genet Genomic Med. 2015. PMID: 26740943 Free PMC article.
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: saletti v. 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.
A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations.
Esposito S, Carecchio M, Tonduti D, Saletti V, Panteghini C, Chiapparini L, Zorzi G, Pantaleoni C, Garavaglia B, Krainc D, Lubbe SJ, Nardocci N, Mencacci NE. Esposito S, et al. Among authors: saletti v. Mov Disord. 2017 Nov;32(11):1646-1647. doi: 10.1002/mds.27175. Epub 2017 Sep 26. Mov Disord. 2017. PMID: 28949041 No abstract available.
77 results