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Page 1
Correction to: Sporadic Fatal Insomnia presenting with agrypnia excitata and rapidly progressive dementia: a case report.
Cannizzaro M, Pieri V, Curti DG, Gueye M, Rugarli G, Napoli G, Cardamone R, Falini A, Perani D, Zucconi M, Casoni F, Giaccone G, Moda F, Di Fede G, Magnani G, Caso F, Filippi M. Cannizzaro M, et al. Among authors: di fede g. J Neurol. 2023 Jul;270(7):3674. doi: 10.1007/s00415-023-11675-5. J Neurol. 2023. PMID: 36976330 No abstract available.
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.
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc.
Puoti G, Giaccone G, Mangieri M, Limido L, Fociani P, Zerbi P, Suardi S, Rossi G, Iussich S, Capobianco R, Di Fede G, Marcon G, Cotrufo R, Filippini G, Bugiani O, Tagliavini F. Puoti G, et al. Among authors: di fede g. J Neuropathol Exp Neurol. 2005 Oct;64(10):902-9. doi: 10.1097/01.jnen.0000183346.19447.55. J Neuropathol Exp Neurol. 2005. PMID: 16215462
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: di fede g. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82. doi: 10.1136/jnnp.2007.115444. J Neurol Neurosurg Psychiatry. 2007. PMID: 18024694 Free PMC article.
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.
Bugiani O, Giaccone G, Rossi G, Mangieri M, Capobianco R, Morbin M, Mazzoleni G, Cupidi C, Marcon G, Giovagnoli A, Bizzi A, Di Fede G, Puoti G, Carella F, Salmaggi A, Romorini A, Patruno GM, Magoni M, Padovani A, Tagliavini F. Bugiani O, et al. Among authors: di fede g. Arch Neurol. 2010 Aug;67(8):987-95. doi: 10.1001/archneurol.2010.178. Arch Neurol. 2010. PMID: 20697050
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. Among authors: di fede g. BMJ Case Rep. 2009;2009:bcr09.2008.0945. doi: 10.1136/bcr.09.2008.0945. Epub 2009 Feb 2. BMJ Case Rep. 2009. PMID: 21686549 Free PMC article.
238 results