Sfoglia per Autore
Status epilepticus-induced pathologic plasticity in a rat model of focal cortical dysplasia
2011 F. Colciaghi, A. Finardi, A. Frasca, S. Balosso, P. Nobili, G. Carriero, D. Locatelli, A. Vezzani, G. Battaglia
In vivo imaging of glia activation using 1H-magnetic resonance spectroscopy to detect putative biomarkers of tissue epileptogenicity
2012 M. Filibian, A. Frasca, D. Maggioni, E. Micotti, A. Vezzani, T. Ravizza
Long-lasting pro-ictogenic effects induced in vivo by rat brain exposure to serum albumin in the absence of concomitant pathology
2012 F. Frigerio, A. Frasca, I. Weissberg, S. Parrella, A. Friedman, A. Vezzani, F.M. Noe'
Striatum and entorhinal cortex atrophy in AD mouse models : MRI comprehensive analysis
2015 E. Micotti, A. Paladini, C. Balducci, D. Tolomeo, A. Frasca, M. Marizzoni, M. Filibian, A. Caroli, G. Valbusa, S. Dix, M. O'Neill, L. Ozmen, C. Czech, J.C. Richardson, G.B. Frisoni, G. Forloni
Toll-like receptor 4-dependent glial cell activation mediates the impairment in memory establishment induced by b-amyloid oligomers in an acute mouse model of Alzheimer’s disease
2017 C. Balducci, A. Frasca, M. Zotti, P. La Vitola, E. Mhillaj, E. Grigoli, M. Iacobellis, F. Grandi, M. Messa, L. Colombo, M. Molteni, L. Trabace, C. Rossetti, M. Salmona, G. Forloni
On-going electroencephalographic rhythms related to cortical arousal in wild-type mice : the effect of aging
2017 C. Del Percio, W. Drinkenburg, S. Lopez, F. Infarinato, J.F. Bastlund, B. Laursen, J.T. Pedersen, D.Z. Christensen, G. Forloni, A. Frasca, F.M. Noã¨, M. Bentivoglio, P.F. Fabene, G. Bertini, V. Colavito, J. Kelley, S. Dix, J.C. Richardson, C. Babiloni
Tyr120Asp mutation alters domain flexibility and dynamics of MeCP2 DNA binding domain leading to impaired DNA interaction : Atomistic characterization of a Rett syndrome causing mutation
2018 I. D'Annessa, A. Gandaglia, E. Brivio, G. Stefanelli, A. Frasca, N. Landsberger, D. Di Marino
Progress in the development of in vivo redox measurements: New tools for longitudinal studies in Rett syndrome
2019 A. Frasca, F. Bedogni, N. Landsberger
A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome
2019 A. Gandaglia, E. Brivio, S. Carli, M. Palmieri, F. Bedogni, G. Stefanelli, A. Bergo, B. Leva, C. Cattaneo, L. Pizzamiglio, M. Cicerone, V. Bianchi, C. Kilstrup-Nielsen, I. D'Annessa, D. Di Marino, P. D'Adamo, F. Antonucci, A. Frasca, N. Landsberger
Splicing mutations impairing CDKL5 expression and activity can be efficiently rescued by U1snRNA-based therapy
2019 D. Balestra, D. Giorgio, M. Bizzotto, M. Fazzari, B.B. Zeev, M. Pinotti, N. Landsberger, A. Frasca
Aminoglycoside drugs induce efficient read-through of CDKL5 nonsense mutations, slightly restoring its kinase activity
2019 M. Fazzari, A. Frasca, F. Bifari, N. Landsberger
Fingolimod modulates dendritic architecture in a BDNF-dependent manner
2020 A. Patnaik, E. Spiombi, A. Frasca, N. Landsberger, M. Zagrebelsky, M. Korte
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders
2020 A. Frasca, E. Spiombi, M. Palmieri, E. Albizzati, M. Valente, A.L.B. Bergo, C. Kilstrup-Nielsen, F. Bianchi, V. Di Carlo, F. Di Cunto, N. Landsberger
Ongoing Electroencephalographic Rhythms Related to Exploratory Movements in Transgenic TASTPM Mice
2020 C. Del Percio, W. Drinkenburg, S. Lopez, M.T. Pascarelli, R. Lizio, G. Noce, R. Ferri, J.F. Bastlund, B. Laursen, D.Z. Christensen, J.T. Pedersen, G. Forloni, A. Frasca, F.M. Noe, P.F. Fabene, G. Bertini, V. Colavito, M. Bentivoglio, J. Kelley, S. Dix, F. Infarinato, A. Soricelli, F. Stocchi, J.C. Richardson, C. Babiloni
Chronic BACE-1 Inhibitor Administration in TASTPM Mice (APP KM670/671NL and PSEN1 M146V Mutation): An EEG Study
2020 S. Lopez, C. Del Percio, G. Forloni, A. Frasca, W.H. Drinkenburg, R. Lizio, G. Noce, R. Ferri, A. Soricelli, F. Stocchi, L. Vacca, R. Bordet, J.C. Richardson, C. Babiloni
In vivo magnetic resonance spectroscopy in the brain of Cdkl5 null mice reveals a metabolic profile indicative of mitochondrial dysfunctions
2021 S. Carli, L. Chaabane, C. Butti, C. De Palma, P. Aimar, C. Salio, A. Vignoli, M. Giustetto, N. Landsberger, A. Frasca
Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals
2022 E. Albizzati, E. Florio, F. Miramondi, I. Sormonta, N. Landsberger, A. Frasca
Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution
2022 A. Frasca, E. Pavlidou, M. Bizzotto, Y. Gao, D. Balestra, M. Pinotti, H.A. Dahl, N.D. Mazarakis, N. Landsberger, M. Kinali
Neural precursor/stem cell-based therapy for Rett syndrome
2022 A. Frasca, F. Miramondi, E. Butti, M. Indrigo, G. DE ROCCO, F. Bedogni, G. Martino, N. Landsberger
A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain
2023 S. Carli, L. Chaabane, G. De Rocco, E. Albizzati, I. Sormonta, S. Calligaro, P. Bonizzi, A. Frasca, N. Landsberger
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