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Candidate gene analysis of semaphorins in patients with Alzheimer's disease.
Published in:
2010
By:
- Villa C;
- Venturelli E;
- Fenoglio C;
- De Riz M;
- Scalabrini D;
- Cortini F;
- Serpente M;
- Cantoni C;
- Bresolin N;
- Scarpini E;
- Galimberti D;
- Villa, Chiara;
- Venturelli, Eliana;
- Fenoglio, Chiara;
- De Riz, Milena;
- Scalabrini, Diego;
- Cortini, Francesca;
- Serpente, Maria;
- Cantoni, Claudia;
- Bresolin, Nereo
Publication type:
journal article
Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred.
Published in:
2011
By:
- Pietroboni AM;
- Fumagalli GG;
- Ghezzi L;
- Fenoglio C;
- Cortini F;
- Serpente M;
- Cantoni C;
- Rotondo E;
- Corti P;
- Carecchio M;
- Bassi M;
- Bresolin N;
- Galbiati D;
- Galimberti D;
- Scarpini E
Publication type:
Journal Article
Cerebrospinal fluid biomarkers in progranulin mutations carriers.
Published in:
2011
By:
- Carecchio M;
- Fenoglio C;
- Cortini F;
- Comi C;
- Benussi L;
- Ghidoni R;
- Borroni B;
- De Riz M;
- Serpente M;
- Cantoni C;
- Franceschi M;
- Albertini V;
- Monaco F;
- Rainero I;
- Binetti G;
- Padovani A;
- Bresolin N;
- Scarpini E;
- Galimberti D
Publication type:
Journal Article
Role of OLR1 and Its Regulating hsa-miR369-3p in Alzheimer's Disease: Genetics and Expression Analysis.
Published in:
2011
By:
- Serpente M;
- Fenoglio C;
- Villa C;
- Cortini F;
- Cantoni C;
- Ridolfi E;
- Clerici F;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Boneschi FM;
- Gallone S;
- Cappa S;
- Binetti G;
- Franceschi M;
- Rainero I;
- Giordana MT;
- Mariani C;
- Bresolin N;
- Scarpini E
Publication type:
Journal Article
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
Published in:
2011
By:
- Villa C;
- Ghezzi L;
- Pietroboni AM;
- Fenoglio C;
- Cortini F;
- Serpente M;
- Cantoni C;
- Ridolfi E;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Jacini F;
- Arighi A;
- Fumagalli GG;
- Mandelli A;
- Binetti G;
- Cappa S;
- Bresolin N;
- Scarpini E;
- Galimberti D
Publication type:
journal article
BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease.
Published in:
2011
By:
- Venturelli E;
- Villa C;
- Fenoglio C;
- Clerici F;
- Marcone A;
- Benussi L;
- Ghidoni R;
- Gallone S;
- Cortini F;
- Serpente M;
- Cantoni C;
- Fumagalli G;
- Ridolfi E;
- Cappa S;
- Binetti G;
- Franceschi M;
- Rainero I;
- Giordana MT;
- Mariani C;
- Bresolin N
Publication type:
Journal Article
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort.
Published in:
European Journal of Neurology, 2010, v. 17, n. 5, p. 740, doi. 10.1111/j.1468-1331.2009.02925.x
By:
- Martinelli-Boneschi, F.;
- Esposito, F.;
- Scalabrini, D.;
- Fenoglio, C.;
- Rodegher, M. E.;
- Brambilla, P.;
- Colombo, B.;
- Ghezzi, A.;
- Capra, R.;
- Collimedaglia, L.;
- Coniglio, G.;
- De Riz, M.;
- Serpente, M.;
- Cantoni, C.;
- Scarpini, E.;
- Martinelli, V.;
- Galimberti, D.;
- Comi, G.
Publication type:
Article
DCUN1D1 is a risk factor for frontotemporal lobar degeneration.
Published in:
European Journal of Neurology, 2009, v. 16, n. 7, p. 870, doi. 10.1111/j.1468-1331.2009.02611.x
By:
- Villa, C.;
- Venturelli, E.;
- Fenoglio, C.;
- Clerici, F.;
- Marcone, A.;
- Benussi, L.;
- Gallone, S.;
- Scalabrini, D.;
- Cortini, F.;
- Serpente, M.;
- Martinelli Boneschi, F.;
- Cappa, S.;
- Binetti, G.;
- Mariani, C.;
- Rainero, I.;
- Giordana, M. T.;
- Bresolin, N.;
- Scarpini, E.;
- Galimberti, D.
Publication type:
Article
Investigating Epigenetic and Neuroimaging Profiles in Bipolar Disorder and Behavioral Variant Frontotemporal Dementia: An integrated epigenetic-neuroimaging approach.
Published in:
2024
By:
- Delvecchio, G.;
- Serpente, M.;
- Di Consoli, L.;
- Rotondo, E.;
- Borraci, V.;
- Scola, E.;
- Triuzi, F. M.;
- Castellani, M.;
- Arighi, A.;
- Scarpini, E.;
- Galimberti, D.;
- Brambilla, P.
Publication type:
Abstract
Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect.
Published in:
GeroScience, 2023, v. 45, n. 3, p. 1557, doi. 10.1007/s11357-023-00746-0
By:
- Visconte, C.;
- Golia, M.T.;
- Fenoglio, C.;
- Serpente, M.;
- Gabrielli, M.;
- Arcaro, M.;
- Sorrentino, F.;
- Busnelli, M.;
- Arighi, A.;
- Fumagalli, G.;
- Rotondo, E.;
- Rossi, P.;
- Arosio, B.;
- Scarpini, E.;
- Verderio, C.;
- Galimberti, D.
Publication type:
Article
Late‐onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation.
Published in:
European Journal of Neurology, 2020, v. 27, n. 12, p. 2630, doi. 10.1111/ene.14506
By:
- Scarioni, M.;
- Arighi, A.;
- Fenoglio, C.;
- Sorrentino, F.;
- Serpente, M.;
- Rotondo, E.;
- Mercurio, M.;
- Marotta, G.;
- Dijkstra, A. A.;
- Pijnenburg, Y. A. L.;
- Scarpini, E.;
- Galimberti, D.
Publication type:
Article

Found: 11