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Familial frontotemporal dementia associated with the novel MAPT mutation T427M.
Giaccone G, Rossi G, Farina L, Marcon G, Di Fede G, Catania M, Morbin M, Sacco L, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: di fede g. J Neurol. 2005 Dec;252(12):1543-5. doi: 10.1007/s00415-005-0879-8. Epub 2005 Jun 6. J Neurol. 2005. PMID: 15940384 No abstract available.
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
Capobianco R, Casalone C, Suardi S, Mangieri M, Miccolo C, Limido L, Catania M, Rossi G, Di Fede G, Giaccone G, Bruzzone MG, Minati L, Corona C, Acutis P, Gelmetti D, Lombardi G, Groschup MH, Buschmann A, Zanusso G, Monaco S, Caramelli M, Tagliavini F. Capobianco R, et al. Among authors: di fede g. PLoS Pathog. 2007 Mar;3(3):e31. doi: 10.1371/journal.ppat.0030031. PLoS Pathog. 2007. PMID: 17352534 Free PMC article.
Atypical tauopathy with massive involvement of the white matter.
Giaccone G, Marcon G, Mangieri M, Morbin M, Rossi G, Fetoni V, Patriarca C, Catania M, Di Fede G, Tagliavini F, Merlin M. Giaccone G, et al. Among authors: di fede g. Neuropathol Appl Neurobiol. 2008 Aug;34(4):468-72. doi: 10.1111/j.1365-2990.2007.00927.x. Epub 2008 Jan 15. Neuropathol Appl Neurobiol. 2008. PMID: 18208485 No abstract available.
A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis.
Di Fede G, Catania M, Morbin M, Rossi G, Suardi S, Mazzoleni G, Merlin M, Giovagnoli AR, Prioni S, Erbetta A, Falcone C, Gobbi M, Colombo L, Bastone A, Beeg M, Manzoni C, Francescucci B, Spagnoli A, Cantù L, Del Favero E, Levy E, Salmona M, Tagliavini F. Di Fede G, et al. Science. 2009 Mar 13;323(5920):1473-7. doi: 10.1126/science.1168979. Science. 2009. PMID: 19286555 Free PMC article.
Good gene, bad gene: new APP variant may be both.
Di Fede G, Catania M, Morbin M, Giaccone G, Moro ML, Ghidoni R, Colombo L, Messa M, Cagnotto A, Romeo M, Stravalaci M, Diomede L, Gobbi M, Salmona M, Tagliavini F. Di Fede G, et al. Prog Neurobiol. 2012 Dec;99(3):281-92. doi: 10.1016/j.pneurobio.2012.06.004. Epub 2012 Jun 19. Prog Neurobiol. 2012. PMID: 22727994 Review.
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38.
Moro ML, Giaccone G, Lombardi R, Indaco A, Uggetti A, Morbin M, Saccucci S, Di Fede G, Catania M, Walsh DM, Demarchi A, Rozemuller A, Bogdanovic N, Bugiani O, Ghetti B, Tagliavini F. Moro ML, et al. Among authors: di fede g. Acta Neuropathol. 2012 Dec;124(6):809-21. doi: 10.1007/s00401-012-1061-x. Epub 2012 Nov 13. Acta Neuropathol. 2012. PMID: 23143229
234 results