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Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
Ambrosini A, D'Onofrio M, Grieco GS, Di Mambro A, Montagna G, Fortini D, Nicoletti F, Nappi G, Sances G, Schoenen J, Buzzi MG, Santorelli FM, Pierelli F. Ambrosini A, et al. Among authors: fortini d, d onofrio m. Neurology. 2005 Dec 13;65(11):1826-8. doi: 10.1212/01.wnl.0000187072.71931.c0. Neurology. 2005. PMID: 16344534
Heterogeneity in migraine: many genes for many phenotypes?
Martini B, Grieco GS, Fortini D, Costa A, Nappi G, Santorelli FM. Martini B, et al. Among authors: fortini d. Funct Neurol. 2001;16(4 Suppl):63-7. Funct Neurol. 2001. PMID: 11996532 Review. No abstract available.
SPG3A: An additional family carrying a new atlastin mutation.
Tessa A, Casali C, Damiano M, Bruno C, Fortini D, Patrono C, Cricchi F, Valoppi M, Nappi G, Amabile GA, Bertini E, Santorelli FM. Tessa A, et al. Among authors: fortini d. Neurology. 2002 Dec 24;59(12):2002-5. doi: 10.1212/01.wnl.0000036902.21438.98. Neurology. 2002. PMID: 12499504
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family.
Casali C, Fabrizi GM, Santorelli FM, Colazza G, Villanova M, Dotti MT, Cavallaro T, Cardaioli E, Battisti C, Manneschi L, DiGennaro GC, Fortini D, Spadaro M, Morocutti C, Federico A. Casali C, et al. Among authors: fortini d. Neurology. 1999 Mar 23;52(5):1103-4. doi: 10.1212/wnl.52.5.1103. Neurology. 1999. PMID: 10102446 No abstract available.
83 results