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Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy.
Rubino E, Zhang M, Mongini T, Boschi S, Vercelli L, Vacca A, Govone F, Gai A, Giordana MT, Grinberg M, Rogaeva E, Rainero I. Rubino E, et al. Among authors: giordana mt. Neurobiol Aging. 2018 Jun;66:181.e1-181.e2. doi: 10.1016/j.neurobiolaging.2018.02.007. Epub 2018 Feb 14. Neurobiol Aging. 2018. PMID: 29519717 Free article.
Response to a letter to the editor.
Rubino E, Zhang M, Mongini T, Boschi S, Vercelli L, Vacca A, Govone F, Gai A, Giordana MT, Grinberg M, Rogaeva E, Rainero I. Rubino E, et al. Among authors: giordana mt. Neurobiol Aging. 2019 Jun;78:195-196. doi: 10.1016/j.neurobiolaging.2019.02.015. Epub 2019 Mar 1. Neurobiol Aging. 2019. PMID: 31027854 No abstract available.
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. Neurology. 2012 Oct 9;79(15):1556-62. doi: 10.1212/WNL.0b013e31826e25df. Epub 2012 Sep 12. Neurology. 2012. PMID: 22972638 Free PMC article.
Late onset bipolar disorder and frontotemporal dementia with mutation in progranulin gene: a case report.
Rubino E, Vacca A, Gallone S, Govone F, Zucca M, Gai A, Ferrero P, Fenoglio P, Giordana MT, Rainero I. Rubino E, et al. Among authors: giordana mt. Amyotroph Lateral Scler Frontotemporal Degener. 2017 Nov;18(7-8):624-626. doi: 10.1080/21678421.2017.1339716. Epub 2017 Jun 30. Amyotroph Lateral Scler Frontotemporal Degener. 2017. PMID: 28664756 Free article.
High Risk of Suicide in Behavioral Variant Frontotemporal Dementia.
Zucca M, Rubino E, Vacca A, Govone F, Gai A, De Martino P, Boschi S, Gentile S, Giordana MT, Rainero I. Zucca M, et al. Among authors: giordana mt. Am J Alzheimers Dis Other Demen. 2019 Jun;34(4):265-271. doi: 10.1177/1533317518817609. Epub 2018 Dec 17. Am J Alzheimers Dis Other Demen. 2019. PMID: 30558441 Free PMC article.
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: giordana mt. Dement Geriatr Cogn Disord. 2009;28(3):239-43. doi: 10.1159/000241876. Epub 2009 Sep 25. Dement Geriatr Cogn Disord. 2009. PMID: 19786775
Metacognitive impairment in patients with episodic and chronic migraine.
Zucca M, Rubino E, Vacca A, De Martino P, Roveta F, Govone F, Gai A, Caglio M, Gentile S, Giordana MT, Rainero I. Zucca M, et al. Among authors: giordana mt. J Clin Neurosci. 2020 Feb;72:119-123. doi: 10.1016/j.jocn.2019.12.048. Epub 2020 Jan 3. J Clin Neurosci. 2020. PMID: 31911106
Subclinical hypothyroidism is associated with migraine: A case-control study.
Rubino E, Rainero I, Garino F, Vicentini C, Govone F, Vacca A, Gai A, Gentile S, Govone G, Ragazzoni F, Pinessi L, Giordana MT, Limone P. Rubino E, et al. Among authors: giordana mt. Cephalalgia. 2019 Jan;39(1):15-20. doi: 10.1177/0333102418769917. Epub 2018 Apr 22. Cephalalgia. 2019. PMID: 29682977
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.
Galimberti D, Fenoglio C, Serpente M, Villa C, Bonsi R, Arighi A, Fumagalli GG, Del Bo R, Bruni AC, Anfossi M, Clodomiro A, Cupidi C, Nacmias B, Sorbi S, Piaceri I, Bagnoli S, Bessi V, Marcone A, Cerami C, Cappa SF, Filippi M, Agosta F, Magnani G, Comi G, Franceschi M, Rainero I, Giordana MT, Rubino E, Ferrero P, Rogaeva E, Xi Z, Confaloni A, Piscopo P, Bruno G, Talarico G, Cagnin A, Clerici F, Dell'Osso B, Comi GP, Altamura AC, Mariani C, Scarpini E. Galimberti D, et al. Among authors: giordana mt. Biol Psychiatry. 2013 Sep 1;74(5):384-91. doi: 10.1016/j.biopsych.2013.01.031. Epub 2013 Mar 7. Biol Psychiatry. 2013. PMID: 23473366 Free article.
177 results