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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: bugiani o. 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.
Neuropathology of Gerstmann-Sträussler-Scheinker disease.
Bugiani O, Giaccone G, Piccardo P, Morbin M, Tagliavini F, Ghetti B. Bugiani O, et al. Microsc Res Tech. 2000 Jul 1;50(1):10-5. doi: 10.1002/1097-0029(20000701)50:1<10::AID-JEMT3>3.0.CO;2-6. Microsc Res Tech. 2000. PMID: 10871543 Review.
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. Arch Neurol. 2010 Aug;67(8):987-95. doi: 10.1001/archneurol.2010.178. Arch Neurol. 2010. PMID: 20697050
Neuronal ceroid lipofuscinosis: detection of atypical forms.
Nardocci N, Morbin M, Bugiani M, Lamantea E, Bugiani O. Nardocci N, et al. Among authors: bugiani m, bugiani o. Neurol Sci. 2000;21(3 Suppl):S57-61. doi: 10.1007/s100720070041. Neurol Sci. 2000. PMID: 11073229
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: bugiani o. 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.
195 results