Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Antonio Indaco"'
Autor:
Cristiano D’Andrea, Federico Angelo Cazzaniga, Edoardo Bistaffa, Andrea Barucci, Marella de Angelis, Martina Banchelli, Edoardo Farnesi, Panagis Polykretis, Chiara Marzi, Antonio Indaco, Pietro Tiraboschi, Giorgio Giaccone, Paolo Matteini, Fabio Moda
Publikováno v:
Translational Neurodegeneration, Vol 12, Iss 1, Pp 1-12 (2023)
Abstract Background The current diagnosis of Alzheimer’s disease (AD) is based on a series of analyses which involve clinical, instrumental and laboratory findings. However, signs, symptoms and biomarker alterations observed in AD might overlap wit
Externí odkaz:
https://doaj.org/article/1a3f7a382ad8441eb6790e942af636f3
Autor:
Federico Angelo Cazzaniga, Edoardo Bistaffa, Chiara Maria Giulia De Luca, Giuseppe Bufano, Antonio Indaco, Giorgio Giaccone, Fabio Moda
Publikováno v:
European Journal of Histochemistry, Vol 65, Iss s1 (2021)
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare and fatal neurodegenerative disorder with an incidence of 1.5 to 2 cases per million population/year. The disease is caused by a proteinaceous infectious agent, named prion (or PrPSc), which arises
Externí odkaz:
https://doaj.org/article/d3974e715441402e9ae289dd92b88efc
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:
Giovanni Bellomo, Antonio Indaco, Davide Chiasserini, Emanuela Maderna, Federico Paolini Paoletti, Lorenzo Gaetani, Silvia Paciotti, Maya Petricciuolo, Fabrizio Tagliavini, Giorgio Giaccone, Lucilla Parnetti, Giuseppe Di Fede
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Amyloid-beta (Aβ) 42/40 ratio, tau phosphorylated at threonine-181 (p-tau), and total-tau (t-tau) are considered core biomarkers for the diagnosis of Alzheimer’s disease (AD). The use of fully automated biomarker assays has been shown to reduce th
Externí odkaz:
https://doaj.org/article/89cf32e948f648c3b09c5af2ae9115b0
Autor:
Eleonora Ficiarà, Silvia Boschi, Shoeb Ansari, Federico D'Agata, Ornella Abollino, Paola Caroppo, Giuseppe Di Fede, Antonio Indaco, Innocenzo Rainero, Caterina Guiot
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
Alzheimer's disease (AD) is the most common form of dementia, characterized by a complex etiology that makes therapeutic strategies still not effective. A true understanding of key pathological mechanisms and new biomarkers are needed, to identify al
Externí odkaz:
https://doaj.org/article/d37da72375de4a7d918f25b07dbdb28c
Autor:
Fabio Moda, Thanh-Nhat T Le, Suzana Aulić, Edoardo Bistaffa, Ilaria Campagnani, Tommaso Virgilio, Antonio Indaco, Luisa Palamara, Olivier Andréoletti, Fabrizio Tagliavini, Giuseppe Legname
Publikováno v:
PLoS Pathogens, Vol 11, Iss 12, p e1005354 (2015)
Prions are infectious proteins that possess multiple self-propagating structures. The information for strains and structural specific barriers appears to be contained exclusively in the folding of the pathological isoform, PrP(Sc). Many recent studie
Externí odkaz:
https://doaj.org/article/da7a8b4b22f046fcb3587e12e443ce88
Autor:
Antonio Indaco, Giuseppe Bufano, Edoardo Bistaffa, Giorgio Giaccone, Fabio Moda, Federico Angelo Cazzaniga, Chiara De Luca
Publikováno v:
European Journal of Histochemistry : EJH
European Journal of Histochemistry, Vol 65, Iss s1 (2021)
European Journal of Histochemistry, Vol 65, Iss s1 (2021)
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare and fatal neurodegenerative disorder with an incidence of 1.5 to 2 cases per million population/year. The disease is caused by a proteinaceous infectious agent, named prion (or PrPSc), which arises
Autor:
Antonio Indaco, Silvia Boschi, Innocenzo Rainero, Giuseppe Di Fede, Caterina Guiot, Ornella Abollino, Shoeb Ansari, Federico D'Agata, Paola Caroppo, Eleonora Ficiarà
Publikováno v:
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience, Vol 13 (2021)
Frontiers in Aging Neuroscience, Vol 13 (2021)
Alzheimer's disease (AD) is the most common form of dementia, characterized by a complex etiology that makes therapeutic strategies still not effective. A true understanding of key pathological mechanisms and new biomarkers are needed, to identify al
Autor:
Luisa Chiapparini, Antonio Indaco, Anna Bersano, Eugenio Parati, Luigi Caputi, Gianluca Marucci, Paola Caroppo, Giuseppe Di Fede, Giorgio Giaccone, Marcella Catania, Emanuela Maderna, Alessandra Erbetta
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-4 (2019)
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-4 (2019)