Sfoglia per Rivista
Body mass index predicts progression of mild cognitive impairment to dementia
2016 I. Cova, F. Clerici, L. Maggiore, S. Pomati, V. Cucumo, R. Ghiretti, D. Galimberti, E. Scarpini, C. Mariani, B. Caracciolo
Cerebrospinal fluid biomarkers in patients carrying thr22fs (g.1977_1980delCACT) mutation in exon 8 of progranulin gene: report of 17 Italian cases
2010 M. Carecchio, C. Fenoglio, L. Benussi, R. Ghidoni, B. Borroni, C. Comi, F. Monaco, G. Binetti, A. Padovani, N. Bresolin, E. Scarpini, D. Galimberti
CHMP5 and BAG1 are protective factors against sporadic Frontotemporal Lobar Degeneration
2010 D. Galimberti, C. Villa, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, S. Cappa, G. Binetti, I. Rainero, N. Bresolin, C. Mariani, E. Scarpini
Comparison of the Alzheimer's disease assessment scale cognitive subscale and the vascular dementia assessment scale in differentiating elderly individuals with different degrees of white matter changes : The Ladis study
2007 R. Ylikoski, H. Jokinen, P. Andersen, O. Salonen, S. Madureira, J. Ferro, F. Barkhof, W. Van Der Flier, R. Schmidt, F. Fazekas, P. Scheltens, G. Waldemar, E. Salvadori, L. Pantoni, D. Inzitari, T. Erkinjuntti
Construct validity of the abbreviated mental test in older medical inpatients
2003 R. Antonelli Incalzi, M. Cesari, C. Pedone, L. Carosella, P.U. Carbonin
Cooperation and networking on white matter disorders: the European Task Force on Age-Related White Matter Changes
1998 T. Erkinjuntti, L. Pantoni, P. Scheltens
Corpus callosum tissue loss and development of motor and global cognitive impairment : the LADIS study
2011 K.S. Frederiksen, E. Garde, A. Skimminge, F. Barkhof, P. Scheltens, E.C.W. Van Straaten, F. Fazekas, H. Baezner, A. Verdelho, J.M. Ferro, T. Erkinjuntti, H. Jokinen, L. Wahlund, J.T. O'Brien, A.M. Basile, L. Pantoni, D. Inzitari, G. Waldemar
Decreased release of the angiogenic peptide vascular endothelial growth factor in alzheimer's disease : Recovering effect with insulin and DHEA sulfate
2005 S.B. Solerte, E. Ferrari, G. Cuzzoni, E. Locatelli, A. Giustina, M. Zamboni, N. Schifino, M. Rondanelli, C. Gazzaruso, M. Fioravanti
Does vascular burden contribute to the progression of mild cognitive impairment to dementia?
2012 F. Clerici, B. Caracciolo, I. Cova, S. Fusari Imperatori, L. Maggiore, D. Galimberti, E. Scarpini, C. Mariani, L. Fratiglioni
Experimental approaches to white matter disease
1998 L. Pantoni
Frequency of the C9ORF72 hexanucleotide repeat expansion in Italian non demented elderly subjects
2012 D. Galimberti, C. Fenoglio, M. Serpente, R. Bonsi, B. Arosio, P. Rossi, C. Villa, S. Cioffi, E. Ridolfi, A. Pietroboni, M. De Riz, F. Jacini, A. Arighi, G. Fumagalli, L. Ghezzi, N. Bresolin, D. Mari, E. Scarpini
Frequency of the chromosome 9 C9ORF72 hexanucleotide repeats in Italian patientswith Frontotemporal Lobar Degeneration
2012 D. Galimberti, C. Fenoglio, M. Serpente, B. Nacmias, S. Sorbi, A. Marcone, S. Cappa, G. Magnani, M. Filippi, F. Agosta, G. Comi, M. Franceschi, I. Rainero, E. Rubino, F. Govone, A. Confaloni, P. Piscopo, G. Bruno, A. Bruni, R. Maletta, A. Cagnin, F. Clerici, C. Mariani, E. Scarpini
GENFI : the GENetic frontotemporal dementia Initiative
2012 F.G. Rohrer J, D. Galimberti, M. Masellis, J. Rowe, B. Borroni, A. Bruni, E. Finger, A. Gerhard, C. Graff, S. Sorbi, J. van Swieten, F. Tagliavini, L. Benussi, G. Binetti, S. Black, T. Chow, R. Colao, E. Dopper, C. Fenoglio, N. Fox, M. Freedman, G. Fumagalli, R. Ghidoni, G. Giaccone, M. Jones, R. Keren, B. Nacmias, S. Ourselin, A. Padovani, M. Pievani, E. Scarpini, D. Tang Wai, M. Tartaglia, J. Warren
GRN Asp22fs mutation is associated with heterogeneous neurodegenerative clinical phenotypes
2010 D. Galimberti, A. Pietroboni, G. Fumagalli, L. Ghezzi, C. Fenoglio, F. Cortini, C. Cantoni, M. Serpente, M.T. Bassi, N. Bresolin, E. Scarpini
hnRNP-A1 rs7967622 is a risk factor for sporadic Frontotemporal Lobar degeneration but not for Alzheimer’s disease
2010 D. Galimberti, E. Venturelli, F. Clerici, R. Ghidoni, S. Gallone, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, N. Bresolin, C. Mariani, E. Scarpini
Is HCRTR2 a genetic risk factor for Alzheimer's disease?
2014 S. Gallone, S. Boschi, E. Rubino, P. De Martino, E. Scarpini, D. Galimberti, C. Fenoglio, P.L. Acutis, M.G. Maniaci, L. Pinessi, I. Rainero
Low cerebrospinal fluid sulfatide predicts progression of white matter lesions : the LADIS study
2012 M. Jonsson, H. Zetterberg, S. Rolstad, A. Edman, A.A. Gouw, M. Bjerke, K. Lind, K. Blennow, L. Pantoni, D. Inzitari, A. Wallin
Neuropsychological predictors of dementia in a three-year follow-up period : data from the ladis study on behalf of the ladis study
2010 S. Madureira, A. Verdelho, C. Moleiro, J.M. Ferro, T. Erkinjuntti, H. Jokinen, L. Pantoni, F. Fazekas, W. Van Der Flier, M. Visser, G. Waldemar, A. Wallin, M. Hennerici, D. Inzitari
On which abilities are category- and letter-fluency grounded? A confirmatory factor analysis of 53 Alzheimer's patients
2013 I. Bizzozero, S. Scotti, F. Clerici, S. Pomati, M. Laiacona, E. Capitani
Polymorphisms in the LOC387715/ARMS2 putative gene and the risk for Alzheimer's disease
2008 L.B. Gatta, M. Vitali, A. Zanola, E. Venturelli, C. Fenoglio, D. Galimberti, E. Scarpini, D. Finazzi
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile