Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sara Maria Portaleone"'
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:
Connor Bargar, Chiara Maria Giulia De Luca, Grazia Devigili, Antonio Emanuele Elia, Roberto Cilia, Sara Maria Portaleone, Wen Wang, Irene Tramacere, Edoardo Bistaffa, Federico Angelo Cazzaniga, Giovanni Felisati, Giuseppe Legname, Alessio Di Fonzo, Rong Xu, Steven Alexander Gunzler, Giorgio Giaccone, Roberto Eleopra, Shu Guang Chen, Fabio Moda
Publikováno v:
Molecular Neurodegeneration, Vol 16, Iss 1, Pp 1-19 (2021)
Abstract Background Detection of the pathological and disease-associated alpha-synuclein (αSynD) in the brain is required to formulate the definitive diagnosis of multiple system atrophy (MSA) and Parkinson’s disease (PD). We recently showed that
Externí odkaz:
https://doaj.org/article/141e44fd167c4a52afa76b73ca2ed5aa
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:
Marco Molteni, Antonio Mario Bulfamante, Carlotta Pipolo, Paolo Lozza, Fabiana Allevi, Antonia Pisani, Matteo Chiapasco, Sara Maria Portaleone, Alberto Scotti, Alberto Maccari, Roberto Borloni, Giovanni Felisati, Alberto Maria Saibene
Publikováno v:
Acta Otorhinolaryngologica Italica, Vol 40, Iss 4, Pp 282-289 (2020)
Externí odkaz:
https://doaj.org/article/1f53ca3673ef48e99ebb904700411802
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:
Edoardo Bistaffa, Alba Marín-Moreno, Juan Carlos Espinosa, Chiara Maria Giulia De Luca, Federico Angelo Cazzaniga, Sara Maria Portaleone, Luigi Celauro, Giuseppe Legname, Giorgio Giaccone, Juan Maria Torres, Fabio Moda
Publikováno v:
eLife, Vol 10 (2021)
Background: Fatal Familial Insomnia (FFI) is a genetic prion disease caused by the D178N mutation in the prion protein gene (PRNP) in coupling phase with methionine at PRNP 129. In 2017, we have shown that the olfactory mucosa (OM) collected from FFI
Externí odkaz:
https://doaj.org/article/4644b327b7314f66a695129f90b90075
Autor:
Maurizio Cariati, Alberto Maccari, Antonia Pisani, Carlotta Pipolo, Giuseppe De Donato, Chiara Spoldi, Alberto Maria Saibene, Giovanni Felisati, Paolo Lozza, Alberto Scotti, Luca Castellani, Sara Maria Portaleone
Publikováno v:
European Archives of Oto-Rhino-Laryngology
Purpose Smell alterations are a symptom of COVID-19 and have been associated with olfactory cleft mucosal thickening (OCMT). Although their pathogenesis is unclear, evidences link them to viral neuroinvasive potential. This study aims at estimating t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2074029e747fc038fc9e09904ee55d0f
http://europepmc.org/articles/PMC7309200
http://europepmc.org/articles/PMC7309200
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:
Edoardo Bistaffa, Alba Marín-Moreno, Juan Carlos Espinosa, Chiara Maria Giulia De Luca, Federico Angelo Cazzaniga, Sara Maria Portaleone, Luigi Celauro, Giuseppe Legname, Giorgio Giaccone, Juan Maria Torres, Fabio Moda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f886e941bf80c2f518615a024255d6a0
https://doi.org/10.7554/elife.65311.sa2
https://doi.org/10.7554/elife.65311.sa2
Autor:
Alberto Maccari, Emanuela Fuccillo, Cecilia Rosso, Alberto Scotti, Luca Castellani, Maria Chiara Tavilla, Antonia Pisani, Paolo Lozza, Carlotta Pipolo, Alberto Maria Saibene, Sara Maria Portaleone, Antonio Mario Bulfamante, Giovanni Felisati, Giuseppe De Donato
Publikováno v:
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery. 279(3)
Purpose Cleft palate children have a higher incidence of otitis media with effusion, more frequent recurrent acute otitis media episodes, and worse conductive hearing losses than non-cleft children. Nevertheless, data on adenoidectomy for middle ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe398bb977197171a22d2a117a01fcc5
https://pubmed.ncbi.nlm.nih.gov/34453572
https://pubmed.ncbi.nlm.nih.gov/34453572