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Page 1
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: pierelli f. Pharmacogenomics. 2014 Mar;15(4):541-9. doi: 10.2217/pgs.14.20. Pharmacogenomics. 2014. PMID: 24624920 Review.
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.
Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM. Grieco GS, et al. Among authors: pierelli f. Neurology. 2004 Jan 13;62(1):103-6. doi: 10.1212/01.wnl.0000104491.66816.77. Neurology. 2004. PMID: 14718707
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: pierelli f. 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. Cephalalgia. 2006 Mar;26(3):324-8. doi: 10.1111/j.1468-2982.2006.01002.x. Cephalalgia. 2006. PMID: 16472340
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.
Criscuolo C, Chessa L, Di Giandomenico S, Mancini P, Saccà F, Grieco GS, Piane M, Barbieri F, De Michele G, Banfi S, Pierelli F, Rizzuto N, Santorelli FM, Gallosti L, Filla A, Casali C. Criscuolo C, et al. Among authors: pierelli f. Neurology. 2006 Apr 25;66(8):1207-10. doi: 10.1212/01.wnl.0000208402.10512.4a. Neurology. 2006. PMID: 16636238
327 results