Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mariacarmela Spinelli"'
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:
Fede, Giuseppe Di, Catania, Marcella, Atzori, Cristiana, Moda, Fabio, Pasquali, Claudio, Indaco, Antonio, Grisoli, Marina, Zuffi, Marta, Guaita, Maria, Testi, Roberto, Taraglio, Stefano, Sessa, Maria, Gusmaroli, Graziano, Mariacarmela Spinelli, Salzano, Giulia, Legname, Giuseppe, Tarletti, Roberto, Godi, Laura, Pocchiari, Maurizio, Tagliavini, Fabrizio, Imperiale, Daniele, Giaccone, Giorgio
Figure S1. Neuropathology of case 3. The neuropathological study on brain sample from case 3 showed findings overlapping those found in case 1 and 4. Severe neuronal loss and spongiform changes (a: frontal cortex, Haematoxylin-Eosin) associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5bc4004bdb505cf86f72a715bc9c4de
Autor:
Graziano Gusmaroli, Antonio Indaco, Maria Sessa, Fabrizio Tagliavini, Giorgio Giaccone, Claudio Pasquali, Marcella Catania, Giulia Salzano, Giuseppe Legname, Maria Cristina Guaita, Cristiana Atzori, Roberto Testi, Daniele Imperiale, Roberto Tarletti, Giuseppe Di Fede, Mariacarmela Spinelli, Fabio Moda, Marina Grisoli, Laura Godi, Maurizio Pocchiari, Marta Zuffi, Stefano Taraglio
Publikováno v:
Acta Neuropathologica Communications
acta neuropathologica communications
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-11 (2019)
acta neuropathologica communications
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-11 (2019)
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 forms. Spor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::081bb9a20fb00bec1c79593bc816f36d
https://pubmed.ncbi.nlm.nih.gov/30606247
https://pubmed.ncbi.nlm.nih.gov/30606247
Autor:
Marco Bacigaluppi, Christian Demitri, Alessandro Sannino, Mariacarmela Spinelli, Luca Peruzzotti-Jametti, Giancarlo Comi, Francesco Corea
Publikováno v:
ResearcherID
The field of neurovascular ultrasound is growing rapidly with new applications. While ultrasound contrast agents were initially used to overcome poor transcranial bone windows for identification of cerebral arteries, newgeneration microbubbles in com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d941f7fe170b5888d3a623114480c5d
http://www.ingentaconnect.com/content/ben/prc/2009/00000004/00000003/art00008
http://www.ingentaconnect.com/content/ben/prc/2009/00000004/00000003/art00008