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Frontotemporal Dementia due to the Novel GRN Arg161GlyfsX36 Mutation.
Gazzina S, Archetti S, Alberici A, Bonomi E, Cosseddu M, Di Lorenzo D, Padovani A, Borroni B. Gazzina S, et al. Among authors: di lorenzo d. J Alzheimers Dis. 2017;57(4):1185-1189. doi: 10.3233/JAD-170066. J Alzheimers Dis. 2017. PMID: 28304311
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: di luca m, di lorenzo d. Neurogenetics. 2008 Jul;9(3):197-205. doi: 10.1007/s10048-008-0127-3. Epub 2008 Apr 8. Neurogenetics. 2008. PMID: 18392865
A PCR-based protocol to accurately size C9orf72 intermediate-length alleles.
Biasiotto G, Archetti S, Di Lorenzo D, Merola F, Paiardi G, Borroni B, Alberici A, Padovani A, Filosto M, Bonvicini C, Caimi L, Zanella I. Biasiotto G, et al. Among authors: di lorenzo d. Mol Cell Probes. 2017 Apr;32:60-64. doi: 10.1016/j.mcp.2016.10.008. Epub 2016 Oct 17. Mol Cell Probes. 2017. PMID: 27765650
Iron and Neurodegeneration: Is Ferritinophagy the Link?
Biasiotto G, Di Lorenzo D, Archetti S, Zanella I. Biasiotto G, et al. Among authors: di lorenzo d. Mol Neurobiol. 2016 Oct;53(8):5542-74. doi: 10.1007/s12035-015-9473-y. Epub 2015 Oct 14. Mol Neurobiol. 2016. PMID: 26468157 Review.
Oxidative stress and cardiovascular disease in dialyzed patients.
Usberti M, Gerardi GM, Gazzotti RM, Benedini S, Archetti S, Sugherini L, Valentini M, Tira P, Bufano G, Albertini A, Di Lorenzo D. Usberti M, et al. Among authors: di lorenzo d. Nephron. 2002 May;91(1):25-33. doi: 10.1159/000057601. Nephron. 2002. PMID: 12021516 Clinical Trial.
89 results