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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: govone f. 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: govone f. 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: govone f. 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: govone f. 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.
Genetic variants in the NOTCH4 gene influence the clinical features of migraine.
Rubino E, Fenoglio P, Gallone S, Govone F, Vacca A, De Martino P, Giobbe ML, Boschi S, Pinessi L, Gentile S, Rainero I. Rubino E, et al. Among authors: govone f. J Headache Pain. 2013 Mar 26;14(1):28. doi: 10.1186/1129-2377-14-28. J Headache Pain. 2013. PMID: 23566281 Free PMC article.
33 results