Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Olga Carletta"'
Autor:
Chiara Maria Giulia De Luca, Antonio Emanuele Elia, Sara Maria Portaleone, Federico Angelo Cazzaniga, Martina Rossi, Edoardo Bistaffa, Elena De Cecco, Joanna Narkiewicz, Giulia Salzano, Olga Carletta, Luigi Romito, Grazia Devigili, Paola Soliveri, Pietro Tiraboschi, Giuseppe Legname, Fabrizio Tagliavini, Roberto Eleopra, Giorgio Giaccone, Fabio Moda
Publikováno v:
Translational Neurodegeneration, Vol 8, Iss 1, Pp 1-14 (2019)
Abstract Background Parkinson’s disease (PD) is a neurodegenerative disorder whose diagnosis is often challenging because symptoms may overlap with neurodegenerative parkinsonisms. PD is characterized by intraneuronal accumulation of abnormal α-sy
Externí odkaz:
https://doaj.org/article/03eb1f542ae049dcb9af8d246ca46cb9
Autor:
Antonio E. Elia, Giuseppe Legname, Grazia Devigili, Olga Carletta, Elena De Cecco, Luigi Romito, Martina Rossi, Fabrizio Tagliavini, Roberto Eleopra, Joanna Narkiewicz, Chiara De Luca, Giulia Salzano, Federico Angelo Cazzaniga, Fabio Moda, Paola Soliveri, Giorgio Giaccone, Sara Maria Portaleone, Edoardo Bistaffa, Pietro Tiraboschi
Publikováno v:
Translational Neurodegeneration, Vol 8, Iss 1, Pp 1-14 (2019)
Translational Neurodegeneration
Translational Neurodegeneration
Background Parkinson’s disease (PD) is a neurodegenerative disorder whose diagnosis is often challenging because symptoms may overlap with neurodegenerative parkinsonisms. PD is characterized by intraneuronal accumulation of abnormal α-synuclein i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa9a2e00f95314ab3581ab75651b1b0
http://link.springer.com/article/10.1186/s40035-019-0164-x
http://link.springer.com/article/10.1186/s40035-019-0164-x
Autor:
Martina Rossi, Giorgio Giaccone, Fabrizio Tagliavini, Edoardo Bistaffa, Fabio Moda, Chiara De Luca, Federico Angelo Cazzaniga, Giuseppe Legname, Olga Carletta, Ilaria Campagnani
Prion diseases are a group of neurodegenerative disorders associated with the conformational conversion of the cellular prion protein (PrPC) into an abnormal misfolded form named PrPSc. Other than accumulating in the brain, PrPSc can bind PrPC and fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb628b9d1d5b987de3c5f397bff3052f
http://hdl.handle.net/20.500.11767/117511
http://hdl.handle.net/20.500.11767/117511
