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Incomplete penetrance in familial Alzheimer's disease with PSEN1 Ala260Gly mutation.
Published in:
Neurological Sciences, 2020, v. 41, n. 8, p. 2263, doi. 10.1007/s10072-020-04421-6
By:
- Piaceri, I.;
- Chiari, A.;
- Galli, C.;
- Bagnoli, S.;
- Ferrari, C.;
- Saavedra, S. Trujillo;
- Molinari, M. A.;
- Vinceti, G.;
- Sorbi, S.;
- Nacmias, B.
Publication type:
Article
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy.
Published in:
Neurological Sciences, 2015, v. 36, n. 5, p. 751, doi. 10.1007/s10072-014-2033-9
By:
- Borroni, B.;
- Turrone, R.;
- Galimberti, D.;
- Nacmias, B.;
- Alberici, A.;
- Benussi, A.;
- Caffarra, P.;
- Caltagirone, C.;
- Cappa, S.;
- Frisoni, G.;
- Ghidoni, R.;
- Marra, C.;
- Padovani, A.;
- Rainero, I.;
- Scarpini, E.;
- Silani, V.;
- Sorbi, S.;
- Tagliavini, F.;
- Tremolizzo, L.;
- Bruni, A.
Publication type:
Article
An APOE Haplotype Associated with Decreased 4 Expression Increases the Risk of Late Onset Alzheimer's Disease.
Published in:
2011
By:
- Lescai F;
- Chiamenti AM;
- Codemo A;
- Pirazzini C;
- D'Agostino G;
- Ruaro C;
- Ghidoni R;
- Benussi L;
- Galimberti D;
- Esposito F;
- Marchegiani F;
- Cardelli M;
- Olivieri F;
- Nacmias B;
- Sorbi S;
- Tagliavini F;
- Albani D;
- Boneschi FM;
- Binetti G;
- Santoro A
Publication type:
Journal Article
SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.
Published in:
2008
By:
- Cozza A;
- Melissari E;
- Iacopetti P;
- Mariotti V;
- Tedde A;
- Nacmias B;
- Conte A;
- Sorbi S;
- Pellegrini S;
- Cozza, Arianna;
- Melissari, Erika;
- Iacopetti, Paola;
- Mariotti, Veronica;
- Tedde, Andrea;
- Nacmias, Benedetta;
- Conte, Angela;
- Sorbi, Sandro;
- Pellegrini, Silvia
Publication type:
journal article
Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.
Published in:
Clinical Genetics, 2012, v. 82, n. 1, p. 83, doi. 10.1111/j.1399-0004.2011.01726.x
By:
- Piaceri, I;
- Del Mastio, M;
- Tedde, A;
- Bagnoli, S;
- Latorraca, S;
- Massaro, F;
- Paganini, M;
- Corrado, A;
- Sorbi, S;
- Nacmias, B
Publication type:
Article
EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia.
Published in:
European Journal of Neurology, 2012, v. 19, n. 9, p. 1159, doi. 10.1111/j.1468-1331.2012.03784.x
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.
Publication type:
Article
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer’s disease.
Published in:
European Journal of Neurology, 2008, v. 15, n. 2, p. 173, doi. 10.1111/j.1468-1331.2007.02021.x
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, Carlo
Publication type:
Article
Are premorbid personality traits linked to the risk of Alzheimer's Disease? A case series of subjects with familial mutation.
Published in:
2000
By:
- Balestrieri, M.;
- Nacmias, B.;
- Sorbi, S.;
- Marcon, G.
Publication type:
journal article
Alzheimer's Disease and Apolipoprotein E in Italya.
Published in:
Annals of the New York Academy of Sciences, 1996, v. 777, n. 1, p. 260, doi. 10.1111/j.1749-6632.1996.tb34429.x
By:
- SORBI, S.;
- NACMIAS, B.;
- FORLEO, P.;
- PIACENTINI, S.;
- AMADUCCI, L.
Publication type:
Article
Fat mass and obesity-associated gene (fto) as a susceptibility factor and moderator of the expression of psychopathological traits of eating disorders.
Published in:
European Psychiatry, 2020, v. 63, p. S125
By:
- Rossi, E.;
- Cassioli, E.;
- Castellini, G.;
- Franzago, M.;
- Bagnoli, S.;
- Lelli, L.;
- Balsamo, M.;
- Mancini, M.;
- Nacmias, B.;
- Ricca, V.;
- Sorbi, S.;
- Antonucci, I.;
- Stuppia, L.;
- Stanghellini, G.
Publication type:
Article
P02-64 Glucocorticoid receptor gene polymorphisms in Italian patients with anorexia and bulimia nervosa
Published in:
2009
By:
- Nacmias, B.;
- Cellini, E.;
- Ricca, V.;
- Castellini, G.;
- Tedde, A.;
- Bagnoli, S.;
- Sorbi, S.
Publication type:
Abstract
Absence of APP717 mutation in Italian FAD families.
Published in:
1992
By:
- Sorbi, S.;
- Tesco, G.;
- Nacmias, B.;
- Mortilla, M.;
- Forleo, P.;
- Latorraca, S.;
- Piersanti, P.;
- Piacentini, S.;
- Amasucci, L.
Publication type:
Letter
Early structural changes in individuals at risk of familial Alzheimer’s disease: a volumetry and magnetization transfer MR imaging study.
Published in:
Journal of Neurology, 2009, v. 256, n. 6, p. 925, doi. 10.1007/s00415-009-5044-3
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.
Publication type:
Article
Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and apoe genotype.
Published in:
2007
By:
- Bracco L;
- Piccini C;
- Baccini M;
- Bessi V;
- Biancucci F;
- Nacmias B;
- Bagnoli S;
- Sorbi S
Publication type:
Journal Article
Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits.
Published in:
2005
By:
- Bracco L;
- Piccini C;
- Moretti M;
- Mascalchi M;
- Sforza A;
- Nacmias B;
- Cellini E;
- Bagnoli S;
- Sorbi S
Publication type:
Journal Article
Alzheimer’s Disease: Role of Size and Location of White Matter Changes in Determining Cognitive Deficits.
Published in:
Dementia & Geriatric Cognitive Disorders, 2005, v. 20, n. 6, p. 358, doi. 10.1159/000088562
By:
- Bracco, L.;
- Piccini, C.;
- Moretti, M. Moretti;
- Mascalchi, M.;
- Sforza, A.;
- Nacmias, B.;
- Cellini, E.;
- Bagnoli, S.;
- Sorbi, S.
Publication type:
Article
Effects of donepezil, galantamine and rivastigmine in 938 Italian patients with Alzheimer's disease: a prospective, observational study.
Published in:
2010
By:
- Santoro A;
- Siviero P;
- Minicuci N;
- Bellavista E;
- Mishto M;
- Olivieri F;
- Marchegiani F;
- Chiamenti AM;
- Benussi L;
- Ghidoni R;
- Nacmias B;
- Bagnoli S;
- Ginestroni A;
- Scarpino O;
- Feraco E;
- Gianni W;
- Cruciani G;
- Paganelli R;
- Di Iorio A;
- Scognamiglio M
Publication type:
journal article
Long-term use of pharmacological treatment in Alzheimer's disease: a retrospective cohort study in real-world clinical practice.
Published in:
European Journal of Clinical Pharmacology, 2022, v. 78, n. 7, p. 1155, doi. 10.1007/s00228-022-03325-y
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
Publication type:
Article
The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death.
Published in:
Cell Death & Differentiation, 2004, v. 11, n. 9, p. 962, doi. 10.1038/sj.cdd.4401415
By:
- Bonafé, M.;
- Salvioli, S.;
- Barbi, C.;
- Trapassi, C.;
- Tocco, F.;
- Storci, C.;
- 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.
Publication type:
Article
ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis.
Published in:
Acta Neurologica Scandinavica, 2009, v. 120, n. 6, p. 439, doi. 10.1111/j.1600-0404.2009.01278.x
By:
- Portaccio, E.;
- Zipoli, V.;
- Goretti, B.;
- Hakiki, B.;
- Nacmias, B.;
- Siracusa, G.;
- Sorbi, S.;
- Amato, M. P.
Publication type:
Article
PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment: a 10‐year follow‐up study.
Published in:
European Journal of Neurology, 2021, v. 28, n. 1, p. 56, doi. 10.1111/ene.14518
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.
Publication type:
Article
Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer's disease: an 11‐year follow‐up study.
Published in:
European Journal of Neurology, 2020, v. 27, n. 5, p. 894, doi. 10.1111/ene.14167
By:
- Mazzeo, S.;
- Padiglioni, S.;
- Bagnoli, S.;
- Carraro, M.;
- Piaceri, I.;
- Bracco, L.;
- Nacmias, B.;
- Sorbi, S.;
- Bessi, V.
Publication type:
Article
In Vitro Response to Fusarium Elicitor and Toxic Substances in Crosses between Resistant and Susceptible Carnation Cultivars.
Published in:
Plant Breeding, 1987, v. 98, n. 4, p. 346, doi. 10.1111/j.1439-0523.1987.tb01141.x
By:
- Buiatti, M.;
- Marcheschi, G.;
- Venturo, R.;
- Bettini, P.;
- Bogani, P.;
- Morpurgo, R.;
- Nacmias, B.;
- Pellegrini, M. G.
Publication type:
Article
The 5-HT[sub2A] --1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres.
Published in:
Molecular Psychiatry, 2002, v. 7, n. 1, p. 90
By:
- Gorwood, P.;
- Ades, J.;
- Bellodi, L.;
- Cellini, E.;
- Collier, D.A.;
- Di Bella, D.;
- Di Bernardo, M.;
- Estivill, X.;
- Fernandez-Aranda, F.;
- Gratacos, M.;
- Hebebrand, J.;
- Hinney, A.;
- Hu, X.;
- Karwautz, A.;
- Kipman, A.;
- Mouren-Simeoni, M.-C.;
- Nacmias, B.;
- Ribases, M.;
- Remschmidt, H.
Publication type:
Article
EFNS-ENS nuorodos apie ligų, susijusių su demencija, diagnostiką ir gydymą.
Published in:
Neurologijos Seminarai, 2013, v. 17, n. 4, p. 309
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.;
- ren, J. D. War;
- Scheltens, P.
Publication type:
Article
HLA A2 allele is associated with age at onset of Alzheimer's disease.
Published in:
1999
By:
- Ballerini, Clara;
- Nacmias, Benedetta;
- Rombolà, Giovanni;
- Marcon, Gabriella;
- Massacesi, Luca;
- Sorbi, Sandro;
- Ballerini, C;
- Nacmias, B;
- Rombolà, G;
- Marcon, G;
- Massacesi, L;
- Sorbi, S
Publication type:
journal article
Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease.
Published in:
1996
By:
- Nacmias, B;
- Tedde, A;
- Latorraca, S;
- Piacentini, S;
- Bracco, L;
- Amaducci, L;
- Guarnieri, B M;
- Petruzzi, C;
- Ortenzi, L;
- Sorbi, S
Publication type:
journal article
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease.
Published in:
1995
By:
- Sorbi, Sandro;
- Nacmias, Benedetta;
- Forleo, Paolo;
- Piacentini, Silvia;
- Latorraca, Stefania;
- Amaducci, Luigi;
- Sorbi, S;
- Nacmias, B;
- Forleo, P;
- Piacentini, S;
- Latorraca, S;
- Amaducci, L
Publication type:
journal article
Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 7, p. 985, doi. 10.1093/hmg/5.7.985
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.
Publication type:
Article
PARKINSON'S DISEASE AND OSTEOPOROSIS.
Published in:
2010
By:
- Raglione, L. M.;
- Sorbi, S.;
- Nacmias, B.
Publication type:
Abstract

Found: 30

Incomplete penetrance in familial Alzheimer's disease with PSEN1 Ala260Gly mutation.

Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy.

An APOE Haplotype Associated with Decreased 4 Expression Increases the Risk of Late Onset Alzheimer's Disease.

SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population.

Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.

EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia.

Codon 129 polymorphism of prion protein gene in sporadic Alzheimer’s disease.

Are premorbid personality traits linked to the risk of Alzheimer's Disease? A case series of subjects with familial mutation.

Alzheimer's Disease and Apolipoprotein E in Italya.

Fat mass and obesity-associated gene (fto) as a susceptibility factor and moderator of the expression of psychopathological traits of eating disorders.

P02-64 Glucocorticoid receptor gene polymorphisms in Italian patients with anorexia and bulimia nervosa

Absence of APP<sub>717</sub> mutation in Italian FAD families.

Early structural changes in individuals at risk of familial Alzheimer’s disease: a volumetry and magnetization transfer MR imaging study.

Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and apoe genotype.

Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits.

Alzheimer’s Disease: Role of Size and Location of White Matter Changes in Determining Cognitive Deficits.

Effects of donepezil, galantamine and rivastigmine in 938 Italian patients with Alzheimer's disease: a prospective, observational study.

Long-term use of pharmacological treatment in Alzheimer's disease: a retrospective cohort study in real-world clinical practice.

The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death.

ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis.

PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment: a 10‐year follow‐up study.

Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer's disease: an 11‐year follow‐up study.

<em>In Vitro</em> Response to <em>Fusarium</em> Elicitor and Toxic Substances in Crosses between Resistant and Susceptible Carnation Cultivars.

The 5-HT[sub2A] --1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres.

EFNS-ENS nuorodos apie ligų, susijusių su demencija, diagnostiką ir gydymą.

HLA A2 allele is associated with age at onset of Alzheimer's disease.

Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease.

Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease.

Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant.

PARKINSON'S DISEASE AND OSTEOPOROSIS.