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Next-generation sequencing approach to hyperCKemia: A 2-year cohort study.
Rubegni A, Malandrini A, Dosi C, Astrea G, Baldacci J, Battisti C, Bertocci G, Donati MA, Dotti MT, Federico A, Giannini F, Grosso S, Guerrini R, Lenzi S, Maioli MA, Melani F, Mercuri E, Sacchini M, Salvatore S, Siciliano G, Tolomeo D, Tonin P, Volpi N, Santorelli FM, Cassandrini D. Rubegni A, et al. Among authors: giannini f. Neurol Genet. 2019 Aug 16;5(5):e352. doi: 10.1212/NXG.0000000000000352. eCollection 2019 Oct. Neurol Genet. 2019. PMID: 31517061 Free PMC article.
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients.
Da Pozzo P, Cardaioli E, Rubegni A, Gallus GN, Malandrini A, Rufa A, Battisti C, Carluccio MA, Rocchi R, Giannini F, Bianchi A, Mancuso M, Siciliano G, Dotti MT, Federico A. Da Pozzo P, et al. Among authors: giannini f. Neurol Sci. 2017 Apr;38(4):563-570. doi: 10.1007/s10072-016-2734-3. Epub 2017 Jan 27. Neurol Sci. 2017. PMID: 28130605
Thalidomide-induced neuropathy: a ganglionopathy?
Giannini F, Volpi N, Rossi S, Passero S, Fimiani M, Cerase A. Giannini F, et al. Neurology. 2003 Mar 11;60(5):877-8. doi: 10.1212/01.wnl.0000049462.03800.b1. Neurology. 2003. PMID: 12629253 No abstract available.
Recurrent Miller Fisher syndrome in children.
Grosso S, Verrotti A, Tei M, Cornacchione S, Giannini F, Balestri P. Grosso S, et al. Among authors: giannini f. Pediatr Neurol. 2014 Mar;50(3):269-71. doi: 10.1016/j.pediatrneurol.2013.10.016. Epub 2013 Oct 31. Pediatr Neurol. 2014. PMID: 24321544 Review.
The Italian multicenter experience with edaravone in amyotrophic lateral sclerosis.
Lunetta C, Moglia C, Lizio A, Caponnetto C, Dubbioso R, Giannini F, Matà S, Mazzini L, Sabatelli M, Siciliano G, Simone IL, Sorarù G, Toriello A, Trojsi F, Vedovello M, D'Ovidio F, Filippi M, Calvo A; and EDARAVALS Study Group. Lunetta C, et al. Among authors: giannini f. J Neurol. 2020 Nov;267(11):3258-3267. doi: 10.1007/s00415-020-09993-z. Epub 2020 Jun 17. J Neurol. 2020. PMID: 32556567 Free article.
529 results