Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ilaria Restelli"'
Autor:
Ilaria Restelli, Letizia Tarantini, Valentina Bollati, Luisella Vigna, Simona Iodice, Benedetta Albetti, Laura Cantone, Matteo Bonzini, Angela Cecilia Pesatori
Publikováno v:
Environmental Research
Background Overweight and obesity are becoming more widespread with alarming projections for the coming years. Obesity may increase susceptibility to the adverse effects of PM exposure, exacerbating the effects on cardiovascular diseases and altering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed310278eb8e0c87e6ee8b0d20a81353
https://doi.org/10.1016/j.envres.2016.11.002
https://doi.org/10.1016/j.envres.2016.11.002
Autor:
Carlo Lovati, Claudio Mariani, Francesca Prato, Diego Albani, Elio Scarpini, Ugo Lucca, Mauro Tettamanti, Daniela Galimberti, Pier Luigi Quadri, Gianluigi Forloni, Ilaria Restelli
Publikováno v:
Journal of Alzheimer's Disease. 18:125-130
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by memory loss and often accompanied during its progression by behavioral and psychological symptoms of dementia (BPSD). We decided to evaluate the association between AD-related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c28a7ff96a84a5096cf3997f61b62e39
https://doi.org/10.3233/jad-2009-1129
https://doi.org/10.3233/jad-2009-1129
Autor:
Chiara Fenoglio, Daniela Galimberti, Ilaria Restelli, Francesco Monaco, Cristoforo Comi, Miryam Carecchio, Elio Scarpini, Claudia Cantoni, Milena De Riz, Eliana Venturelli, Francesca Cortini, Ilaria Guidi, Nereo Bresolin
Publikováno v:
Journal of the Neurological Sciences. 287:291-293
Progranulin (GRN) mutations are associated with different clinical phenotypes, including Frontotemporal Lobar Degeneration (FTLD), Corticobasal Degeneration and Alzheimer's disease (AD). In addition, the range of age at onset is very wide and patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a2ab4a542647d1e01b729222b80dc73
https://doi.org/10.1016/j.jns.2009.07.011
https://doi.org/10.1016/j.jns.2009.07.011
Autor:
Eliana Venturelli, Roberta Ghidoni, Filippo Martinelli Boneschi, Chiara Fenoglio, Stefano F. Cappa, Francesca Clerici, Elio Scarpini, Alessandra Marcone, Giuliano Binetti, Innocenzo Rainero, Nereo Bresolin, Ilaria Restelli, Chiara Villa, Claudio Mariani, Daniela Galimberti, Francesca Cortini, Maria Serpente, Salvatore Gallone, Diego Scalabrini, Maria Teresa Giordana, Luisa Benussi
Publikováno v:
Journal of Alzheimer's disease : JAD. 19(1)
Mutations in the progranulin gene (GRN) are responsible for familial FTLD with ubiquitin pathology (FTLD-U). However, there are controversial data regarding the contribution of GRN variability to sporadic FTLD. We carried out an association study in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7662d72cd73121e08e7ab12afe375bc5
https://pubmed.ncbi.nlm.nih.gov/20061636
https://pubmed.ncbi.nlm.nih.gov/20061636
Autor:
Stefano F. Cappa, Luca Perini, Francesca Clerici, Giuliano Binetti, Eliana Venturelli, Elio Scarpini, Alessandra Marcone, Chiara Villa, Daniela Galimberti, Francesca Cortini, Diego Scalabrini, Luisa Benussi, Claudio Mariani, Chiara Fenoglio, Nereo Bresolin, Ilaria Restelli
The distribution of the MCP-1 A-2518G single nucleotide polymorphisms (SNP) was analyzed in a population of 212 patients with frontotemporal lobar degeneration (FTLD) compared with 203 age-matched controls. A significantly decreased allelic frequency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::109da3b9a43723e1e8a3a45a9d67df71
http://hdl.handle.net/10281/281904
http://hdl.handle.net/10281/281904
Autor:
Ilaria Restelli, Stefano F. Cappa, M. T. Giordana, Claudio Mariani, Chiara Villa, Nereo Bresolin, Innocenzo Rainero, Daniela Galimberti, Diego Scalabrini, A. Mandelli, Francesca Clerici, Eliana Venturelli, Salvatore Gallone, Chiara Fenoglio, Roberta Ghidoni, Francesca Cortini, Elio Scarpini, Alessandra Marcone, G. Binetti
Background and aims: Neuronal nitric oxide synthase (NOS)1 C276T polymorphism was shown to increase the risk for frontotemporal lobar degeneration (FTLD). In the brain, both NOS1 and NOS3 (endothelial isoform) have been detected. The distribution of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d616b537354167e0fa8391ffc1fa96a
http://hdl.handle.net/10281/281908
http://hdl.handle.net/10281/281908