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O Bugiani

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Articles 149
Citations 2477
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Recent Articles
1.
Forloni G, Chiesa R, Bugiani O, Salmona M, Tagliavini F
Neuropathol Appl Neurobiol . 2019 Jan; 45(5):430-440. PMID: 30635947
A quarter of a century ago, we proposed an innovative approach to study the pathogenesis of prion disease, one of the most intriguing biomedical problems that remains unresolved. The synthesis...
2.
Bruni A, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, et al.
Neurology . 2010 Feb; 74(10):798-806. PMID: 20164095
Objective: Large kindreds segregating familial Alzheimer disease (FAD) offer the opportunity of studying clinical variability as observed for presenilin 1 (PSEN1) mutations. Two early-onset FAD (EOFAD) Calabrian families with PSEN1...
3.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, et al.
J Neurol Neurosurg Psychiatry . 2007 Nov; 78(12):1379-82. PMID: 18024694
An atypical case of sporadic Creutzfeldt-Jakob disease (CJD) is described in a 78-year-old woman homozygous for methionine at codon 129 of the prion protein (PrP) gene. The neuropathological signature was...
4.
Bugiani O
Neurol Sci . 2007 Nov; 28(5):241-4. PMID: 17972037
Background: Frontotemporal degeneration (FTD) is the most common cause of dementia after Alzheimer's disease. To date, it has been addressed with intensive and intense research. Objective: To report on the...
5.
Franzini A, Marras C, Tringali G, Leone M, Ferroli P, Bussone G, et al.
Acta Neurochir Suppl . 2007 Aug; 97(Pt 2):399-406. PMID: 17691328
Chronic high frequency stimulation (HFS) of the posteromedial hypothalamus (PMH) has been the first direct therapeutic application of functional neuroimaging data in a restorative reversible procedure for the treatment of...
6.
Giaccone G, Mangieri M, Capobianco R, Limido L, Hauw J, Haik S, et al.
Neurobiol Aging . 2007 Jun; 29(12):1864-73. PMID: 17560687
Cerebral accumulation of hyperphosphorylated tau (phospho-tau) occurs in several neurodegenerative conditions including Alzheimer disease. In prion diseases, phospho-tau deposition has been described in a rare genetic form, Gerstmann-Sträussler-Scheinker disease, but...
7.
Baba Y, Baker M, Le Ber I, Brice A, Maeck L, Kohlhase J, et al.
J Neural Transm (Vienna) . 2007 Feb; 114(7):947-50. PMID: 17318302
In 9 patients with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) with a P301S tau mutation, the predominant phenotype was frontotemporal dementia in 3 and parkinsonism in 6....
8.
Bugiani O
Neurol Sci . 2006 May; 27 Suppl 1:S44-6. PMID: 16708184
Dementia is due to lesions destroying a large amount of circuits anatomically connected with, or functionally related to, the associative areas of the cortex and the limbic structures. Dementia is...
9.
Mascalchi M, Gavazzi C, Morbin M, Giaccone G, Arnetoli G, Zappoli R, et al.
AJNR Am J Neuroradiol . 2006 May; 27(5):1037-9. PMID: 16687539
CT and MR imaging showed diffuse changes of the frontal white matter and genu of the corpus callosum with minimal atrophy and no contrast enhancement in a 41-year-old woman with...
10.
Visani E, Agazzi P, Scaioli V, Giaccone G, Binelli S, Canafoglia L, et al.
Clin Neurophysiol . 2005 Mar; 116(4):895-904. PMID: 15792899
Objective: To characterise flash visual evoked potentials (FVEPs) in 20 patients with Creutzfeldt-Jacob disease (CJD), and assess the relationships between spontaneous EEG patterns and the responses to individual stimuli. Methods:...