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Novel exon 1 progranulin gene variant in Alzheimer's disease.
Cortini F, Fenoglio C, Guidi I, Venturelli E, Pomati S, Marcone A, Scalabrini D, Villa C, Clerici F, Dalla Valle E, Mariani C, Cappa S, Bresolin N, Scarpini E, Galimberti D. Cortini F, et al. Among authors: marcone a. Eur J Neurol. 2008 Oct;15(10):1111-7. doi: 10.1111/j.1468-1331.2008.02266.x. Epub 2008 Aug 26. Eur J Neurol. 2008. PMID: 18752597
Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease.
Anchisi D, Borroni B, Franceschi M, Kerrouche N, Kalbe E, Beuthien-Beumann B, Cappa S, Lenz O, Ludecke S, Marcone A, Mielke R, Ortelli P, Padovani A, Pelati O, Pupi A, Scarpini E, Weisenbach S, Herholz K, Salmon E, Holthoff V, Sorbi S, Fazio F, Perani D. Anchisi D, et al. Among authors: marcone a. Arch Neurol. 2005 Nov;62(11):1728-33. doi: 10.1001/archneur.62.11.1728. Arch Neurol. 2005. PMID: 16286547
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Ghidoni R, Cortini F, Scalabrini D, Gallone S, Rainero I, Mandelli A, Restelli I, Binetti G, Cappa S, Mariani C, Giordana MT, Bresolin N, Scarpini E, Galimberti D. Venturelli E, et al. Among authors: marcone a. Eur J Neurol. 2009 Jan;16(1):37-42. doi: 10.1111/j.1468-1331.2008.02335.x. Eur J Neurol. 2009. PMID: 19087148
91 results