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Page 1
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: fenoglio p. Dement Geriatr Cogn Disord. 2009;28(3):239-43. doi: 10.1159/000241876. Epub 2009 Sep 25. Dement Geriatr Cogn Disord. 2009. PMID: 19786775
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Rubino E, Rainero I, Chiò A, Rogaeva E, Galimberti D, Fenoglio P, Grinberg Y, Isaia G, Calvo A, Gentile S, Bruni AC, St George-Hyslop PH, Scarpini E, Gallone S, Pinessi L; TODEM Study Group. Rubino E, et al. Among authors: fenoglio p. Neurology. 2012 Oct 9;79(15):1556-62. doi: 10.1212/WNL.0b013e31826e25df. Epub 2012 Sep 12. Neurology. 2012. PMID: 22972638 Free PMC article.
Tumor necrosis factor-alpha gene and cerebral aneurysms.
Fontanella M, Rainero I, Gallone S, Rubino E, Fenoglio P, Valfrè W, Garbossa D, Carlino C, Ducati A, Pinessi L. Fontanella M, et al. Among authors: fenoglio p. Neurosurgery. 2007 Apr;60(4):668-72; discussion 672-3. doi: 10.1227/01.NEU.0000255417.93678.49. Neurosurgery. 2007. PMID: 17415203
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: fenoglio p. 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.
KCNK18 (TRESK) genetic variants in Italian patients with migraine.
Rainero I, Rubino E, Gallone S, Zavarise P, Carli D, Boschi S, Fenoglio P, Savi L, Gentile S, Benna P, Pinessi L, Dalla Volta G. Rainero I, et al. Among authors: fenoglio p. Headache. 2014 Oct;54(9):1515-22. doi: 10.1111/head.12439. Headache. 2014. PMID: 25324165
20 results