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692 results

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Page 1
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.
Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM. Casali C, et al. Among authors: nappi g. Neurology. 2004 Jan 27;62(2):262-8. doi: 10.1212/wnl.62.2.262. Neurology. 2004. PMID: 14745065
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: nappi g. Neurology. 2002 Dec 24;59(12):2002-5. doi: 10.1212/01.wnl.0000036902.21438.98. Neurology. 2002. PMID: 12499504
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: nappi g. Funct Neurol. 2001;16(4 Suppl):63-7. Funct Neurol. 2001. PMID: 11996532 Review. No abstract available.
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: nappi g. Neurology. 2005 Dec 13;65(11):1826-8. doi: 10.1212/01.wnl.0000187072.71931.c0. Neurology. 2005. PMID: 16344534
A novel ATP1A2 mutation in a family with FHM type II.
Pierelli F, Grieco GS, Pauri F, Pirro C, Fiermonte G, Ambrosini A, Costa A, Buzzi MG, Valoppi M, Caltagirone C, Nappi G, Santorelli FM. Pierelli F, et al. Among authors: nappi g. Cephalalgia. 2006 Mar;26(3):324-8. doi: 10.1111/j.1468-2982.2006.01002.x. Cephalalgia. 2006. PMID: 16472340
692 results