Search Results - "Nacmias, B."

A proof-of-concept study applying machine learning methods to putative risk factors for eating disorders: results from the multi-centre European project on healthy eating by Krug, I, Linardon, J, Greenwood, C, Youssef, G, Treasure, J, Fernandez-Aranda, F, Karwautz, A, Wagner, G, Collier, D, Anderluh, M, Tchanturia, K, Ricca, V, Sorbi, S, Nacmias, B, Bellodi, L, Fuller-Tyszkiewicz, M

“…Despite a wide range of proposed risk factors and theoretical models, prediction of eating disorder (ED) onset remains poor. This study undertook the first…”
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EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia by Sorbi, S., Hort, J., Erkinjuntti, T., Fladby, T., Gainotti, G., Gurvit, H., Nacmias, B., Pasquier, F., Popescu, B. O., Rektorova, I., Religa, D., Rusina, R., Rossor, M., Schmidt, R., Stefanova, E., Warren, J. D., Scheltens, P.

“…Background and objectives The last version of the EFNS dementia guidelines is from 2007. In 2010, the revised guidelines for Alzheimer's disease (AD) were…”
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Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer’s disease: an 11‐year follow‐up study by Mazzeo, S., Padiglioni, S., Bagnoli, S., Carraro, M., Piaceri, I., Bracco, L., Nacmias, B., Sorbi, S., Bessi, V.

“…Background and purpose Subjective cognitive decline (SCD) is a self‐experienced decline in cognitive capacity with normal performance on standardized cognitive…”
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Long-term use of pharmacological treatment in Alzheimer’s disease: a retrospective cohort study in real-world clinical practice by Lombardi, G, Lombardi, N, Bettiol, A, Crescioli, G, Ferrari, C, Lucidi, G, Polito, C, Berti, V, Bessi, V, Bagnoli, S, Nacmias, B, Vannacci, A, Sorbi, S

“…Purpose To assess the impact of long-term use of different drugs commonly prescribed in Alzheimer’s disease (AD) on its clinical course and to identify…”
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PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment: a 10‐year follow‐up study by Bessi, V., Giacomucci, G., Mazzeo, S., Bagnoli, S., Padiglioni, S., Balestrini, J., Tomaiuolo, G., Piaceri, I., Carraro, M., Bracco, L., Sorbi, S., Nacmias, B.

“…Clock genes have been implicated in sleep‐wake cycle alterations and neurodegenerative diseases, but the role of PER2 C111G on cognition and on the risk of…”
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MCI conversion to dementia and the APOE genotype: A prediction study with FDG-PET by MOSCONI, L, PERANI, D, BORRONI, B, FRANCESCHI, M, BRACCO, L, PUPI, A, SORBI, S, HERHOLZ, K, NACMIAS, B, HOLTHOFF, V, SALMON, E, BARON, J.-C, DE CRISTOFARO, M. T. R, PADOVANI, A

“…To investigate whether the combination of fluoro-2-deoxy-d-glucose (FDG) PET measures with the APOE genotype would improve prediction of the conversion from…”
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Incomplete penetrance in familial Alzheimer’s disease with PSEN1 Ala260Gly mutation by Piaceri, I., Chiari, A., Galli, C., Bagnoli, S., Ferrari, C., Saavedra, S. Trujillo, Molinari, M. A., Vinceti, G., Sorbi, S., Nacmias, B.

“…Presenilin1 (PSEN1) gene is the most common known genetic cause of early-onset familial Alzheimer’s disease. We describe an Italian family with the known…”
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Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene by Rogaev, E. I, Sherrington, R, Rogaeva, E. A, Levesque, G, Ikeda, M, Liang, Y, Chi, H, Lin, C, Holman, K, Tsuda, T, Mar, L, Sorbi, S, Nacmias, B, Piacentini, S, Amaducci, L, Chumakov, I, Cohen, D, Lannfelt, L, Fraser, P. E, Rommens, J. M, George-Hyslop, P. H. St

“…We report the cloning of a novel gene (E5-1) encoded on chromosome 1 which has substantial nucleotide and amino-acid sequence similarity to the S182 gene on…”
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Alzheimer's disease: genetic basis and amyloid imaging as endophenotype by Berti, V, Nacmias, B, Bagnoli, S, Sorbi, S

“…To date, all known Alzheimer's disease genes influence amyloid β (Aβ). Imaging of Aβ deposition in the human brain using positron emission tomography (PET)…”
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Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis by Piaceri, I, Del Mastio, M, Tedde, A, Bagnoli, S, Latorraca, S, Massaro, F, Paganini, M, Corrado, A, Sorbi, S, Nacmias, B

“…Piaceri I, Del Mastio M, Tedde A, Bagnoli S, Latorraca S, Massaro F, Paganini M, Corrado A, Sorbi S, Nacmias B. Clinical heterogeneity in Italian patients with…”
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The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death by Bonafé, M, Salvioli, S, Barbi, C, Trapassi, C, Tocco, F, Storci, G, Invidia, L, Vannini, I, Rossi, M, Marzi, E, Mishto, M, Capri, M, Olivieri, F, Antonicelli, R, Memo, M, Uberti, D, Nacmias, B, Sorbi, S, Monti, D, Franceschi, C

“…A common arginine to proline polymorphism is harboured at codon 72 of the human p53 gene. In this investigation, we found that fibroblasts and lymphocytes…”
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Early structural changes in individuals at risk of familial Alzheimer’s disease: a volumetry and magnetization transfer MR imaging study by Ginestroni, A., Battaglini, M., Della Nave, R., Moretti, M., Tessa, C., Giannelli, M., Caffarra, P., Nacmias, B., Bessi, V., Sorbi, S., Bracco, L., De Stefano, N., Mascalchi, M.

“…Presenilin 1 (PS1) mutation carriers provide the opportunity to asses early features of neurodegeneration in familial Alzheimer’s disease (AD). Gray matter…”
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Metabolic interaction between ApoE genotype and onset age in Alzheimer’s disease: implications for brain reserve by Mosconi, L, Herholz, K, Prohovnik, I, Nacmias, B, De Cristofaro, M T R, Fayyaz, M, Bracco, L, Sorbi, S, Pupi, A

“…Background: Clinically apparent Alzheimer’s disease (AD) is thought to result when brain tissue damage exceeds a critical threshold of “brain reserve”, a…”
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Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits by Bracco, L, Piccini, C, Moretti, M, Mascalchi, M, Sforza, A, Nacmias, B, Cellini, E, Bagnoli, S, Sorbi, S

“…This study investigated the contribution that white matter changes (WMCs) make to clinical and cognitive features in Alzheimer's disease (AD), independently of…”
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Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease by CARRIERI, Giuseppina, BONAFE, Massimiliano, FERACO, Emidio, ANDREEV, Kirill F, YASHIN, Anatoli I, FRANCESCHI, Claudio, DE BENEDICTIS, Giovanna, DE LUCA, Maria, ROSE, Giuseppina, VARCASIA, Ottavia, BRUNI, Amalia, MALETTA, Raffaele, NACMIAS, Benedetta, SORBI, Sandro, CORSONELLO, Francesco

“…Allele epsilon4 of the nuclear APOE gene is a leading genetic risk factor for sporadic Alzheimer's disease (AD). Moreover, an allele-specific effect of APOE…”
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Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease by Poleggi, A., Bizzarro, A., Acciarri, A., Antuono, P., Bagnoli, S., Cellini, E., Forno, G. Dal, Giannattasio, C., Lauria, A., Matera, M. G., Nacmias, B., Puopolo, M., Seripa, D., Sorbi, S., Wekstein, D. R., Pocchiari, M., Masullo, C.

“…Codon 129 polymorphism of the prion protein gene represents a major genetic risk factor for Creutzfeldt‐Jakob disease (CJD). Both CJD and Alzheimer’s disease…”
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ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis by Portaccio, E., Zipoli, V., Goretti, B., Hakiki, B., Nacmias, B., Siracusa, G., Sorbi, S., Amato, M. P.

“…Background –  No study has assessed the association between apolipoproteinE (APOE) and multiple sclerosis (MS) forms grouped by also taking into account…”
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Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant by Sherrington, R., Froelich, S., Sorbi, S., Campion, D., Chi, H., Rogaeva, E. A., Levesque, G., Rogaev, E. I., Lin, C., Liang, Y., Ikeda, M., Mar, L., Brice, A., Agid, Y., Percy, M.E., Clerget-Darpoux, F., Piacentini, S., Marcon, G., Nacmias, B., Amaducci, L., Frebourg, T., Lannfelt, L., Rommens, J. M., St George-Hyslop, P. H.

“…Missense mutations in the presenilin 2 (PS-2) gene on chromosome 1 were sought by direct nucleotide sequence analysis of the open reading frame of 60 pedigrees…”
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The 5-HT2A -1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres by GORWOOD, P, ADES, J, HEBEBRAND, J, HINNEY, A, HU, X, KARWAUTZ, A, KIPMAN, A, MOUREN-SIMEONI, M-C, NACMIAS, B, RIBASES, M, REMSCHMIDT, H, RICCA, V, BELLODI, L, ROTELLA, C. M, SORBI, S, TREASURE, J, CELLINI, E, COLLIER, D. A, DI BELLA, D, DI BERNARDO, M, ESTIVILL, X, FERNANDEZ-ARANDA, F, GRATACOS, M

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P02-64 Glucocorticoid receptor gene polymorphisms in Italian patients with anorexia and bulimia nervosa by Nacmias, B, Cellini, E, Ricca, V, Castellini, G, Tedde, A, Bagnoli, S, Sorbi, S

“…The etiopathogenesis of eating disorders (ED) is complex and poorly understood. The hypothalamic-pituitary-adrenal (HPA) axis, involved in the biological…”
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