Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Marcella, Catania"'
Autor:
Riccardo Milani, Lucio Aniello Mazzeo, Daniela Vismara, Ilaria Salemi, Emanuele Dainese, Emanuela Maderna, Elisa Pellencin, Marcella Catania, Nicole Campanella, Giuseppe Di Fede, Giorgio Giaccone, Andrea Salmaggi
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-5 (2023)
Abstract Cerebral amyloid angiopathy (CAA) is a small vessel disease, causing spontaneous intracerebral hemorrhage (ICH) in the elderly. It is strongly associated with Alzheimer disease (AD), as most CAA patients show deposition of Aβ—i.e. the bas
Externí odkaz:
https://doaj.org/article/b64433c1006a433bb8b15dc2a1de51fb
Autor:
Federico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, Sara Maria Portaleone, Marcella Catania, Veronica Redaelli, Irene Tramacere, Giuseppe Bufano, Martina Rossi, Paola Caroppo, Anna Rita Giovagnoli, Pietro Tiraboschi, Giuseppe Di Fede, Roberto Eleopra, Grazia Devigili, Antonio Emanuele Elia, Roberto Cilia, Michele Fiorini, Matilde Bongianni, Giulia Salzano, Luigi Celauro, Federico Giuseppe Quarta, Angela Mammana, Giuseppe Legname, Fabrizio Tagliavini, Piero Parchi, Gianluigi Zanusso, Giorgio Giaccone, Fabio Moda
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
Externí odkaz:
https://doaj.org/article/f36d14b05e854b90b710f3688c676a6c
Autor:
Federico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, Sara Maria Portaleone, Marcella Catania, Veronica Redaelli, Irene Tramacere, Giuseppe Bufano, Martina Rossi, Paola Caroppo, Anna Rita Giovagnoli, Pietro Tiraboschi, Giuseppe Di Fede, Roberto Eleopra, Grazia Devigili, Antonio Emanuele Elia, Roberto Cilia, Michele Fiorini, Matilde Bongianni, Giulia Salzano, Luigi Celauro, Federico Giuseppe Quarta, Angela Mammana, Giuseppe Legname, Fabrizio Tagliavini, Piero Parchi, Gianluigi Zanusso, Giorgio Giaccone, Fabio Moda
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disorder caused by the conformational conversion of the prion protein (PrPC) into an abnormally folded form, named prion (or PrPSc). The combination of the polymorphism at codon 12
Externí odkaz:
https://doaj.org/article/4a98baad86204ee3be173b36f764ec46
Autor:
Giorgio Giaccone, Emanuela Maderna, Gianluca Marucci, Marcella Catania, Alessandra Erbetta, Luisa Chiapparini, Antonio Indaco, Paola Caroppo, Anna Bersano, Eugenio Parati, Giuseppe Di Fede, Luigi Caputi
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-4 (2019)
Externí odkaz:
https://doaj.org/article/8e167e785e6e4cafbf12e33e0d62c733
Autor:
Giuseppe Di Fede, Marcella Catania, Cristiana Atzori, Fabio Moda, Claudio Pasquali, Antonio Indaco, Marina Grisoli, Marta Zuffi, Maria Cristina Guaita, Roberto Testi, Stefano Taraglio, Maria Sessa, Graziano Gusmaroli, Mariacarmela Spinelli, Giulia Salzano, Giuseppe Legname, Roberto Tarletti, Laura Godi, Maurizio Pocchiari, Fabrizio Tagliavini, Daniele Imperiale, Giorgio Giaccone
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-11 (2019)
Abstract Prion diseases are neurodegenerative disorders which are caused by an accumulation of the abnormal, misfolded prion protein known as scrapie prion protein (PrPSc). These disorders are unique as they occur as sporadic, genetic and acquired fo
Externí odkaz:
https://doaj.org/article/46afdf2fd23547ffa41d811b6d180715
Autor:
Antonio Longobardi, Luisa Benussi, Roland Nicsanu, Sonia Bellini, Clarissa Ferrari, Claudia Saraceno, Roberta Zanardini, Marcella Catania, Giuseppe Di Fede, Rosanna Squitti, Giuliano Binetti, Roberta Ghidoni
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Alzheimer’s disease (AD), frontotemporal dementia (FTD), and dementia with Lewy bodies (DLB) are the three major neurodegenerative dementias. In this study, we provide evidence that an alteration in extracellular vesicles (EVs) release is common ac
Externí odkaz:
https://doaj.org/article/c67abb90d12c461887e0d76b551c50b0
Autor:
Antonio Longobardi, Roland Nicsanu, Sonia Bellini, Rosanna Squitti, Marcella Catania, Pietro Tiraboschi, Claudia Saraceno, Clarissa Ferrari, Roberta Zanardini, Giuliano Binetti, Giuseppe Di Fede, Luisa Benussi, Roberta Ghidoni
Publikováno v:
Cells, Vol 11, Iss 3, p 462 (2022)
Alzheimer’s disease (AD), dementia with Lewy bodies (DLB) and frontotemporal dementia (FTD) represent the three major neurodegenerative dementias characterized by abnormal brain protein accumulation. In this study, we investigated extracellular ves
Externí odkaz:
https://doaj.org/article/6d67c436a316484191d4f7f84a837cc6
Autor:
Mirta Borin, Claudia Saraceno, Marcella Catania, Erika Lorenzetto, Valeria Pontelli, Anna Paterlini, Silvia Fostinelli, Anna Avesani, Giuseppe Di Fede, Gianluigi Zanusso, Luisa Benussi, Giuliano Binetti, Simone Zorzan, Roberta Ghidoni, Mario Buffelli, Silvia Bolognin
Publikováno v:
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-17 (2018)
Abstract One of the earliest pathological features characterizing Alzheimer’s disease (AD) is the loss of dendritic spines. Among the many factors potentially mediating this loss of neuronal connectivity, the contribution of Rho-GTPases is of parti
Externí odkaz:
https://doaj.org/article/11d0fb5036e34d868ddf83de50c56590
Autor:
Federica Cencini, Marcella Catania, Giuseppe Di Fede, Giacomina Rossi, Katia Khouri Chalouhi, Chiara Manfredi, Giorgio Giaccone, Pietro Tiraboschi, Anna Bersano, Elisabetta Groppo, Chiara Rosci, Lucia Tancredi, Laura Campiglio, Amedeo De Grado, Alberto Priori, Emma Scelzo
Publikováno v:
European Journal of Neurology. 29:3139-3146
Publikováno v:
Frontiers in Aging Neuroscience, Vol 11 (2019)
Alzheimer’s disease (AD) is the most common form of dementia. It’s a chronic and untreatable neurodegenerative disease with irreversible progression and has important social and economic implications in terms of direct medical and social care cos
Externí odkaz:
https://doaj.org/article/e57ece2105094c5995dd644bb10b04d9