CORTINI, FRANCESCA
CORTINI, FRANCESCA
Dipartimento di Scienze Cliniche e di Comunità
A Rare Cause of Juvenile Stroke: Extracranial Carotid Artery Aneurysm with Venous Complete Reconstruction of the Carotid Bifurcation
2018 M. Domanin, S. Lanfranconi, S. Romagnoli, L. Runza, F. Cortini, G.P. Comi, L. Gabrielli
PICALM gene methylation in blood of Alzheimer's disease patients is associated with cognitive decline
2018 R. Mercorio, L. Pergoli, D. Galimberti, C. Favero, M. Carugno, E. Dalla Valle, F. Barretta, F. Cortini, E. Scarpini, V. Bollati, A.C. Pesatori
Ehlers-Danlos Syndrome classical type: A novel COL5A2 missense mutation with possible additive effect of a COL5A1 stop-gain mutation in a strongly correlated phenotype
2018 F. Cortini, C. Villa, B. Marinelli, S. Franchetti, M. Seia, A.C. Pesatori, N. Montano, A. Bassotti
A New COL3A1 Mutation in Ehlers-Danlos Syndrome Vascular Type with Different Phenotypes in the Same Family
2017 F. Cortini, B. Marinelli, S. Romi, A. Seresini, A.C. Pesatori, M. Seia, N. Montano, A. Bassotti
Bone involvement in adult patients affected with Ehlers-Danlos syndrome
2016 C. Eller-Vainicher, A.F. Bassotti, A. Imeraj, E. Cairoli, F.M. Ulivieri, F. Cortini, M. Dubini, E.B.L. Marinelli, A. Spada, I. Chiodini
Effects of particulate matter exposure on multiple sclerosis hospital admission in Lombardy region, Italy
2016 L. Angelici, M. Piola, T. Cavalleri, G. Randi, F. Cortini, R. Bergamaschi, A.A. Baccarelli, P.A. Bertazzi, A.C. Pesatori, V. Bollati
Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers-Danlos syndrome with severe intestinal involvement: a case report
2016 F. Cortini, B. Marinelli, M. Seia, B. De Giorgio, A.C. Pesatori, N. Montano, A. Bassotti
Repetitive element hypermethylation in multiple sclerosis patients
2016 K.Y. Neven, M. Piola, L. Angelici, F. Cortini, C. Fenoglio, D. Galimberti, A.C. Pesatori, E. Scarpini, V. Bollati
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia
2012 D. Galimberti, B. Dell'Osso, C. Fenoglio, C. Villa, F. Cortini, M. Serpente, S. Kittel Schneider, J. Weigl, M. Neuner, J. Volkert, C. Leonhard, D.G. Olmes, J. Kopf, C. Cantoni, E. Ridolfi, C. Palazzo, L. Ghezzi, N. Bresolin, A.C. Altamura, E. Scarpini, A. Reif
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 D. Galimberti, C. Villa, L. Ghezzi, A. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E. Scarpini
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 C. Villa, L. Ghezzi, A.M. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G.G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E. Scarpini, D. Galimberti
Cerebrospinal Fluid Biomarkers in Progranulin Mutations Carriers
2011 M. Carecchio, C. Fenoglio, F. Cortini, C. Comi, L. Benussi, R. Ghidoni, B. Borroni, M. De Riz, M. Serpente, C. Cantoni, M. Franceschi, V. Albertini, F. Monaco, I. Rainero, G. Binetti, A. Padovani, N. Bresolin, E. Scarpini, D. Galimberti
Expression and genetic analysis of miRNAs involved in CD4+cell activation in patients with multiple sclerosis
2011 C. Fenoglio, C. Cantoni, M. De Riz, E. Ridolfi, F. Cortini, M. Serpente, C. Villa, C. Comi, F. Monaco, L. Mellesi, S. Valzelli, N. Bresolin, D. Galimberti, E. Scarpini
Novel progranulin mutation in a sporadic case of frontotemporal dementia parkinsonism presentino with asymmetric rest tremor and cognitive decline
2011 M. Carecchio, D. Galimberti, F. Cortini, C. Cantoni, E.A. Scarpini, E. Terazzi, F. Monaco
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease
2011 E. Venturelli, C. Villa, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, F. Cortini, M. Serpente, C. Cantoni, G. Fumagalli, E. Ridolfi, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype
2011 C. Villa, L. Ghezzi, A.M. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G.G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E.A. Scarpini, D. Galimberti
Causal frontotemporal de generation mutations : a novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 C. Villa, L. Ghezzi, A.M. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G.G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E.A. Scarpini, D. Galimberti
Oligodendrocyte lineage transcription factor-2 role in Alzheimer’s disease : association and expression analysis
2011 F. Cortini, C. Fenoglio, F. Clerici, L. Benussi, R. Ghidoni, S. Gallone, A. Marcone, C. Villa, M. Serpente, C. Cantoni, E. Ridolfi, M. Franceschi, G. Binetti, I. Rainero, S. Cappa, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
OLR1 and its regulatory miR-369-3p : genetics and expression analysis
2011 M. Serpente, C. Fenoglio, F. Clerici, R. Ghidoni, L. Benussi, S. Gallone, A. Marcone, C. Villa, F. Cortini, C. Cantoni, E. Ridolfi, M. Franceschi, G. Binetti, I. Rainero, S. Cappa, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
Oligodendrocyte Lineage Transcription Factor 2 role in Alzheimer’s disease : association and expression analysis
2011 F. Cortini, C. Fenoglio, F. Clerici, L. Benussi, R. Ghidoni, S. Gallone, A. Marcone, C. Villa, M. Serpente, C. Cantoni, E. Ridolfi, M. Franceschi, G. Binetti, I. Rainero, S. Cappa, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti