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408 results

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Page 1
FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration.
Cantoni C, Fenoglio C, Cortini F, Venturelli E, Villa C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Franceschi M, Cappa S, Binetti G, Mariani C, Rainero I, Giordana MT, Bresolin N, Scarpini E, Galimberti D. Cantoni C, et al. Among authors: ghidoni r. J Alzheimers Dis. 2010;19(4):1317-22. doi: 10.3233/JAD-2010-1328. J Alzheimers Dis. 2010. PMID: 20061612
Alzheimer disease-associated cystatin C variant undergoes impaired secretion.
Benussi L, Ghidoni R, Steinhoff T, Alberici A, Villa A, Mazzoli F, Nicosia F, Barbiero L, Broglio L, Feudatari E, Signorini S, Finckh U, Nitsch RM, Binetti G. Benussi L, et al. Among authors: ghidoni r. Neurobiol Dis. 2003 Jun;13(1):15-21. doi: 10.1016/s0969-9961(03)00012-3. Neurobiol Dis. 2003. PMID: 12758063
Frontotemporal dementia: impact of P301L tau mutation on a healthy carrier.
Alberici A, Gobbo C, Panzacchi A, Nicosia F, Ghidoni R, Benussi L, Hock C, Papassotiropoulos A, Liberini P, Growdon JH, Frisoni GB, Villa A, Zanetti O, Cappa S, Fazio F, Binetti G. Alberici A, et al. Among authors: ghidoni r. J Neurol Neurosurg Psychiatry. 2004 Nov;75(11):1607-10. doi: 10.1136/jnnp.2003.021295. J Neurol Neurosurg Psychiatry. 2004. PMID: 15489396 Free PMC article.
Reduction of Ca2+ stores and capacitative Ca2+ entry is associated with the familial Alzheimer's disease presenilin-2 T122R mutation and anticipates the onset of dementia.
Giacomello M, Barbiero L, Zatti G, Squitti R, Binetti G, Pozzan T, Fasolato C, Ghidoni R, Pizzo P. Giacomello M, et al. Among authors: ghidoni r. Neurobiol Dis. 2005 Apr;18(3):638-48. doi: 10.1016/j.nbd.2004.10.016. Neurobiol Dis. 2005. PMID: 15755689
In contrast to the majority of FAD-linked PS1 mutations, which cause an overload of intracellular Ca2+ pools, the FAD-linked PS2 mutation M239I reduces Ca2+ release from intracellular stores [Zatti, G., Ghidoni, R., Barbiero, L., Binetti, G., Pozzan, T., Fasolato, C …
In contrast to the majority of FAD-linked PS1 mutations, which cause an overload of intracellular Ca2+ pools, the FAD-linked PS2 mutation M2 …
408 results