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Disease-related cortical thinning in presymptomatic granulin mutation carriers.
Borrego-Écija S, Sala-Llonch R, van Swieten J, Borroni B, Moreno F, Masellis M, Tartaglia C, Graff C, Galimberti D, Laforce R Jr, Rowe JB, Finger E, Vandenberghe R, Tagliavini F, de Mendonça A, Santana I, Synofzik M, Ducharme S, Levin J, Danek A, Gerhard A, Otto M, Butler C, Frisoni G, Sorbi S, Heller C, Bocchetta M, Cash DM, Convery RS, Moore KM, Rohrer JD, Sanchez-Valle R; Genetic FTD Initiative GENFI. Borrego-Écija S, et al. Among authors: galimberti d. Neuroimage Clin. 2021;29:102540. doi: 10.1016/j.nicl.2020.102540. Epub 2020 Dec 29. Neuroimage Clin. 2021. PMID: 33418170 Free PMC article.
Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series.
Borroni B, Archetti S, Alberici A, Agosti C, Gennarelli M, Bigni B, Bonvicini C, Ferrari M, Bellelli G, Galimberti D, Scarpini E, Di Lorenzo D, Caimi L, Caltagirone C, Di Luca M, Padovani A. Borroni B, et al. Among authors: galimberti d. Neurogenetics. 2008 Jul;9(3):197-205. doi: 10.1007/s10048-008-0127-3. Epub 2008 Apr 8. Neurogenetics. 2008. PMID: 18392865
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
Fenoglio C, Galimberti D, Cortini F, Kauwe JS, Cruchaga C, Venturelli E, Villa C, Serpente M, Scalabrini D, Mayo K, Piccio LM, Clerici F, Albani D, Mariani C, Forloni G, Bresolin N, Goate AM, Scarpini E. Fenoglio C, et al. Among authors: galimberti d. J Alzheimers Dis. 2009;18(3):603-12. doi: 10.3233/JAD-2009-1170. J Alzheimers Dis. 2009. PMID: 19625741 Free PMC article.
The CST3 B haplotype is associated with frontotemporal lobar degeneration.
Benussi L, Ghidoni R, Galimberti D, Boccardi M, Fenoglio C, Scarpini E, Frisoni GB, Binetti G. Benussi L, et al. Among authors: galimberti d. Eur J Neurol. 2010 Jan;17(1):143-6. doi: 10.1111/j.1468-1331.2009.02767.x. Epub 2009 Aug 5. Eur J Neurol. 2010. PMID: 19674067
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease.
Carecchio M, Fenoglio C, De Riz M, Guidi I, Comi C, Cortini F, Venturelli E, Restelli I, Cantoni C, Bresolin N, Monaco F, Scarpini E, Galimberti D. Carecchio M, et al. Among authors: galimberti d. J Neurol Sci. 2009 Dec 15;287(1-2):291-3. doi: 10.1016/j.jns.2009.07.011. Epub 2009 Aug 14. J Neurol Sci. 2009. PMID: 19683260 Free article.
599 results