Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Emanuela Maderna"'
Autor:
Gaia Giordano, Mirko Mattia, Lucie Biehler-Gomez, Michele Boracchi, Stefania Tritella, Emanuela Maderna, Alessandro Porro, Massimiliano Marco Corsi Romanelli, Antonia Francesca Franchini, Paolo Maria Galimberti, Fabrizio Slavazzi, Francesco Sardanelli, Domenico Di Candia, Cristina Cattaneo
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract In this paper, we present the results of toxicological analyses of preserved brain tissue and bone samples from the remains of the seventeenth century patients of the Ospedale Maggiore, the main hospital in Milan and one of the most innovati
Externí odkaz:
https://doaj.org/article/ee9f2f615bbe465d9ad4f8c304fafd72
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:
Patrizia Bossolasco, Sara Cimini, Emanuela Maderna, Donatella Bardelli, Laura Canafoglia, Tiziana Cavallaro, Martina Ricci, Vincenzo Silani, Gianluca Marucci, Giacomina Rossi
Publikováno v:
Neurobiology of Disease, Vol 175, Iss , Pp 105891- (2022)
Heterozygous mutations in the gene coding for progranulin (GRN) cause frontotemporal lobar degeneration (FTLD) while homozygous mutations are linked to neuronal ceroidolipofuscinosis (NCL). While both FTLD/NCL pathological hallmarks were mostly inves
Externí odkaz:
https://doaj.org/article/e840ac6da1584dd5b39f1a168967932f
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:
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:
Salmaggi, Chiara Vasco, Ambra Rizzo, Chiara Cordiglieri, Elena Corsini, Emanuela Maderna, Emilio Ciusani, Andrea
Publikováno v:
Cancers; Volume 15; Issue 11; Pages: 3045
Metastatic brain disease (MBD) has seen major advances in clinical management, focal radiation therapy approaches and knowledge of biological factors leading to improved prognosis. Extracellular vesicles (EVs) have been found to play a role in tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::dd983a990a35441905ede52e2859ac02
Publikováno v:
The Bioarchaeology of Cardiovascular Disease ISBN: 9781108648561
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2376510836cfa80bea385824efd0b7a
https://doi.org/10.1017/9781108648561.017
https://doi.org/10.1017/9781108648561.017
Autor:
Paola Saveri, Stefania Magri, Emanuela Maderna, Francesca Balistreri, Raffaella Lombardi, Claudia Ciano, Fabio Moda, Barbara Garavaglia, Chiara Reale, Giuseppe Lauria Pinter, Franco Taroni, Davide Pareyson, Chiara Pisciotta
Publikováno v:
European Journal of Neurology. 29:2056-2065
Mutations in DNAJB2 are associated with autosomal recessive hereditary motor neuropathies/ Charcot-Marie-Tooth disease type 2 (CMT2). We describe an Italian family with CMT2 due to a homozygous DNAJB2 mutation and provide insight into the pathomechan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7079e99cb137de4e694efcc27683fbd5
https://doi.org/10.1111/ene.15326
https://doi.org/10.1111/ene.15326
Autor:
Mirko Mattia, Lucie Biehler-Gomez, Emanuela Sguazza, Paolo Maria Galimberti, Folco Vaglienti, Daniele Gibelli, Pasquale Poppa, Giulia Caccia, Marco Caccianiga, Stefano Vanin, Laura Manthey, Richard L. Jantz, Domenico Di Candia, Emanuela Maderna, Giuliana Albini, Sachin Pawaskar, Franklin Damann, Anna Maria Fedeli, Elena Belgiovine, Daniele Capuzzo, Fabrizio Slavazzi, Cristina Cattaneo
Publikováno v:
Med Hist
The Ospedale Maggiore, known as Ca’ Granda, was founded in 1456 by will of Francesco Sforza, Duke of Milan, and was considered for almost five centuries a model for Milanese, Italian and even European healthcare. Attracting patients from all over E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a67c6a2d156570867c1e9ec28cc12c9
https://doi.org/10.1017/mdh.2021.40
https://doi.org/10.1017/mdh.2021.40
Autor:
Carla Boccaccio, Gaetano Finocchiaro, Paolo M. Comoglio, Bianca Pollo, Emanuela Maderna, Monica Patanè, Paola Porrati, Antonio D'Ambrosio, Gigliola Reato, Paolo Luraghi, Raffaella Albano, Francesca Orzan, Serena Pellegatta, Enzo Medico, Elena Casanova, Francesca De Bacco
XLS file - 12K, Mutations of PTEN, TP53, and NF1 genes in glioblastoma neurospheres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ea91ab742b2b44d8bb797c0d28f2bae
https://doi.org/10.1158/0008-5472.22393740
https://doi.org/10.1158/0008-5472.22393740