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Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degeneration.
Gallone S, Giordana MT, Scarpini E, Rainero I, Rubino E, Fenoglio P, Galimberti D, Grifoni S, Venturelli E, Acutis PL, Peletto S, Maniaci MG, Ferrero P, Zotta M, Pinessi L. Gallone S, et al. Among authors: pinessi l. Dement Geriatr Cogn Disord. 2009;28(3):239-43. doi: 10.1159/000241876. Epub 2009 Sep 25. Dement Geriatr Cogn Disord. 2009. PMID: 19786775
Association between major mood disorders and the hypocretin receptor 1 gene.
Rainero I, Ostacoli L, Rubino E, Gallone S, Picci LR, Fenoglio P, Negro E, Rosso C, De Martino P, De Marchi M, Furlan PM, Pinessi L. Rainero I, et al. Among authors: pinessi l. J Affect Disord. 2011 May;130(3):487-91. doi: 10.1016/j.jad.2010.10.033. Epub 2010 Nov 10. J Affect Disord. 2011. PMID: 21071097 Free article.
Is HCRTR2 a genetic risk factor for Alzheimer's disease?
Gallone S, Boschi S, Rubino E, De Martino P, Scarpini E, Galimberti D, Fenoglio C, Acutis PL, Maniaci MG, Pinessi L, Rainero I. Gallone S, et al. Among authors: pinessi l. Dement Geriatr Cogn Disord. 2014;38(3-4):245-53. doi: 10.1159/000359964. Epub 2014 Jun 25. Dement Geriatr Cogn Disord. 2014. PMID: 24969517
Apolipoprotein E gene polymorphisms in patients with migraine.
Rainero I, Grimaldi LM, Salani G, Valfrè W, Savi L, Rivoiro C, Gentile S, Pinessi L. Rainero I, et al. Among authors: pinessi l. Neurosci Lett. 2002 Jan 11;317(2):111-3. doi: 10.1016/s0304-3940(01)02432-6. Neurosci Lett. 2002. PMID: 11755252
186 results