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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: grieco gs. Neurology. 2005 Dec 13;65(11):1826-8. doi: 10.1212/01.wnl.0000187072.71931.c0. Neurology. 2005. PMID: 16344534
The wolframin His611Arg polymorphism influences medication overuse headache.
Di Lorenzo C, Sances G, Di Lorenzo G, Rengo C, Ghiotto N, Guaschino E, Perrotta A, Santorelli FM, Grieco GS, Troisi A, Siracusano A, Pierelli F, Nappi G, Casali C. Di Lorenzo C, et al. Among authors: grieco gs. Neurosci Lett. 2007 Sep 13;424(3):179-84. doi: 10.1016/j.neulet.2007.07.037. Epub 2007 Aug 6. Neurosci Lett. 2007. PMID: 17719176
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: grieco gs. Cephalalgia. 2006 Mar;26(3):324-8. doi: 10.1111/j.1468-2982.2006.01002.x. Cephalalgia. 2006. PMID: 16472340
Pharmacogenomics of episodic migraine: time has come for a step forward.
Viana M, Terrazzino S, Genazzani AA, Grieco GS, Cargnin S, Santorelli FM, Pierelli F, Tassorelli C, Nappi G, Di Lorenzo C. Viana M, et al. Among authors: grieco gs. Pharmacogenomics. 2014 Mar;15(4):541-9. doi: 10.2217/pgs.14.20. Pharmacogenomics. 2014. PMID: 24624920 Review.
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: grieco gs. Funct Neurol. 2001;16(4 Suppl):63-7. Funct Neurol. 2001. PMID: 11996532 Review. No abstract available.
48 results