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Mostrati risultati da 1 a 20 di 109
Titolo Data di pubblicazione Autore(i) File
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 2006 Elena Cellini;Andrea Tedde;Silvia Bagnoli;Benedetta Nacmias;Silvia Piacentini;Valentina Bessi;Laura Bracco;Sandro Sorbi
Hypometabolism exceeds atrophy in presymptomatic early-onset familial Alzheimer's disease 2006 MOSCONI L.; SORBI S.; DE LEON M.J.; LI Y.; NACMIAS B.; MYOUNG P.S.; TSUI W.; GINESTRONI A.; BESSI V.; FAYYAZZ M.; CAFFARRA P.; PUPI A.
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 2007 Nacmias B; Bagnoli S; Tedde A; Cellini E; Bessi V; Guarnieri B; Ortensi L; Piacentini S; Bracco L; Sorbi S
Pattern and progression of cognitive decline in Alzheimer's disease:role of premorbid intelligence and ApoE genotype 2007 Bracco L; Piccini C; Baccini M; Bessi V; Biancucci F; Nacmias B; Bagnoli S; Sorbi S.
Correlati Neurali del Deficit Mnesico: Studio VBM e DTI in soggetti affetti da Disturbo Soggettivo di Memoria, Mild Cognitive Impairment e Malattia di Alzheimer 2010 V.Bessi
Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease 2010 Tedde A; Bagnoli S; Piaceri I; Lucenteforte E; Bessi V; Bracco L; Mugelli A; Sorbi S; Nacmias B.
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. 2010 Nacmias B; Tedde A; Bagnoli S; Lucenteforte E; Cellini E; Piaceri I; Guarnieri BM; Bessi V; Bracco L; Sorbi S.
Semantic dementia associated with mutation V363I in the tau gene. 2010 Bessi V.; Bagnoli S.; Nacmias B.; Tedde A.; Sorbi S.; Bracco L.
Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI). 2011 Marini S; Bagnoli S; Bessi V; Tedde A; Bracco L; Sorbi S; Nacmias B.
A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene 2012 Sandro Marini; Giulia Lucidi; Andrea Tedde; Valentina Bessi;Benedetta Nacmias
Suitability of neuropsychological tests in patients with vascular dementia (VaD). 2012 Bagnoli S; Failli Y; Piaceri I; Rinnoci V; Bessi V; Tedde A; Nacmias B; Sorbi S.
Regional analysis of the magnetization transfer ratio of the brain in mild Alzheimer disease and amnestic mild cognitive impairment 2013 Mascalchi, M; Ginestroni, A; Bessi, V; Toschi, N; Padiglioni, S; Ciulli, S; Tessa, C; Giannelli, M; Bracco, L; Diciotti, S
A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats 2013 van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P
Tomm40 polymorphisms in Italian Alzheimer’s disease and frontotemporal dementia patients 2013 Silvia Bagnoli;Irene Piaceri;Andrea Tedde;Valentina Bessi;Laura Bracco;Sandro Sorbi;Benedetta Nacmias
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 2013 Daniela Galimberti;Chiara Fenoglio;Maria Serpente;Chiara Villa;Rossana Bonsi;Andrea Arighi;Giorgio G. Fumagalli;Roberto Del Bo;Amalia C. Bruni;Maria Anfossi;Alessandra Clodomiro;Chiara Cupidi;Benedetta Nacmias;Sandro Sorbi;Irene Piaceri;Silvia Bagnoli;Valentina Bessi;Alessandra Marcone;Chiara Cerami;Stefano F. Cappa;Massimo Filippi;Federica Agosta;Giuseppe Magnani;Giancarlo Comi;Massimo Franceschi;Innocenzo Rainero;Maria Teresa Giordana;Elisa Rubino;Patrizia Ferrero;Ekaterina Rogaeva;Zhengrui Xi;Annamaria Confaloni;Paola Piscopo;Giuseppe Bruno;Giuseppina Talarico;Annachiara Cagnin;Francesca Clerici;Bernardo Dell’Osso;Giacomo P. Comi;A. Carlo Altamura;Claudio Mariani;Elio Scarpini
Do Cholinesterase Inhibitors Act Primarily on Attention Deficit? A Naturalistic Study in Alzheimer's Disease Patients 2014 Bracco, Laura; Bessi, Valentina; Padiglioni, Sonia; Marini, Sandro; Pepeu, Giancarlo
Mutation analysis of patients with neurodegenerative disorders using NeuroX array 2015 Mahdi Ghani;Anthony E. Lang;Lorne Zinman;Benedetta Nacmias;Sandro Sorbi;Valentina Bessi;Andrea Tedde;Maria Carmela Tartaglia;Ezequiel I. Surace;Christine Sato;Danielle Moreno;Zhengrui Xi;Rachel Hung;Mike A. Nalls;Andrew Singleton;Peter St George-Hyslop;Ekaterina Rogaeva
Low MT ratio in hippocampus of amnestic MCI patients who will progress to AD 2016 Mascalchi, Mario; Bessi, Valentina; Ginestroni, Andrea; Toschi, Nicola; Ciulli, Stefano; Padiglioni, Sonia; Bracco, Laura; Diciotti, Stefano
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease 2017 de Roeck, Arne; van Den Bossche, Tobi; van der Zee, Julie; Verheijen, Jan; de Coster, Wouter; van Dongen, Jasper; Dillen, Lubina; Baradaran-Heravi, Yalda; Heeman, Bavo; Sanchez-Valle, Raquel; Lladó, Albert; Nacmias, Benedetta; Sorbi, Sandro; Gelpi, Ellen; Grau-Rivera, Oriol; Gómez-Tortosa, Estrella; Pastor, Pau; Ortega-Cubero, Sara; Pastor, Maria A.; Graff, Caroline; Thonberg, Håkan; Benussi, Luisa; Ghidoni, Roberta; Binetti, Giuliano; de Mendonça, Alexandre; Martins, Madalena; Borroni, Barbara; Padovani, Alessandro; Almeida, Maria Rosário; Santana, Isabel; Diehl-Schmid, Janine; Alexopoulos, Panagiotis; Clarimon, Jordi; Lleó, Alberto; Fortea, Juan; Tsolaki, Magda; Koutroumani, Maria; Matěj, Radoslav; Rohan, Zdenek; de Deyn, Peter; Engelborghs, Sebastiaan; Cras, Patrick; van Broeckhoven, Christine; Sleegers, Kristel; Bessi, Valentina; Bagnoli, Silvia; Do Couto, Frederico Simões; Verdelho, Ana; Fratiglioni, Laura; Padovani, Alessandro; Rohan, Zdenek; Razquin, Cristina; Lorenzo, Elena; Iglesias, Elena; Seijo-Martínez, Manuel; Rene, Ramon; Gascon, Jordi; Campdelacreu, Jaume; Blesa, Rafael
Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation 2018 Bessi, Valentina*; Piaceri, Irene; Padiglioni, Sonia; Bagnoli, Silvia; Berti, Valentina; Sorbi, Sandro; Nacmias, Benedetta
Mostrati risultati da 1 a 20 di 109
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