Eirini Kanata
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Explore the profile of Eirini Kanata including associated specialties, affiliations and a list of published articles.
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24
Citations
308
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Recent Articles
11.
Schmitz M, Candelise N, Kanata E, Llorens F, Thune K, Villar-Pique A, et al.
Mol Neurobiol
. 2019 Dec;
57(4):1863-1874.
PMID: 31848935
Prion diseases, such as the sporadic Creutzfeldt-Jakob disease (sCJD), are a class of fatal neurodegenerative disorders. Currently, there is no efficient treatment or therapy available. Hence, the search for molecules...
12.
Kanata E, Llorens F, Dafou D, Dimitriadis A, Thune K, Xanthopoulos K, et al.
Proc Natl Acad Sci U S A
. 2019 Sep;
116(39):19727-19735.
PMID: 31492812
Prion diseases are fatal neurodegenerative disorders caused by misfolding of the normal prion protein into an infectious cellular pathogen. Clinically characterized by rapidly progressive dementia and accounting for 85% of...
13.
Angelis G, Zayed D, Karioti A, Lazari D, Kanata E, Sklaviadis T, et al.
Chemistry
. 2019 Aug;
25(56):12916-12919.
PMID: 31397017
Inorganic cells bearing calcium silicate membranes were prepared and resembled closed chemical gardens. It was demonstrated that these inorganic cells can successfully be loaded with natural products, proteins and plasmid...
14.
Kanata E, Golanska E, Villar-Pique A, Karsanidou A, Dafou D, Xanthopoulos K, et al.
J Clin Neurosci
. 2018 Oct;
60:124-127.
PMID: 30309804
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of human prion disease. It is invariably fatal and displays a short clinical disease stage. The key event in sCJD is...
15.
Kanata E, Thune K, Xanthopoulos K, Ferrer I, Dafou D, Zerr I, et al.
Front Aging Neurosci
. 2018 Aug;
10:220.
PMID: 30083102
Prion diseases are transmissible progressive neurodegenerative conditions characterized by rapid neuronal loss accompanied by a heterogeneous neuropathology, including spongiform degeneration, gliosis and protein aggregation. The pathogenic mechanisms and the origins...
16.
Zerr I, Schmitz M, Karch A, Villar-Pique A, Kanata E, Golanska E, et al.
Alzheimers Dement
. 2018 Feb;
14(6):751-763.
PMID: 29391125
Introduction: Neurofilament light (NFL) levels in the cerebrospinal fluid are increased in several neurodegenerative dementias. However, their diagnostic accuracy in the differential diagnostic context is unknown. Methods: Cerebrospinal fluid NFL...
17.
Llorens F, Thune K, Marti E, Kanata E, Dafou D, Diaz-Lucena D, et al.
PLoS Pathog
. 2018 Jan;
14(1):e1006802.
PMID: 29357384
Increasing evidence indicates that microRNAs (miRNAs) are contributing factors to neurodegeneration. Alterations in miRNA signatures have been reported in several neurodegenerative dementias, but data in prion diseases are restricted to...
18.
Llorens F, Thune K, Tahir W, Kanata E, Diaz-Lucena D, Xanthopoulos K, et al.
Mol Neurodegener
. 2017 Nov;
12(1):83.
PMID: 29126445
Background: YKL-40 (also known as Chitinase 3-like 1) is a glycoprotein produced by inflammatory, cancer and stem cells. Its physiological role is not completely understood but YKL-40 is elevated in...
19.
Llorens F, Kruse N, Schmitz M, Gotzmann N, Golanska E, Thune K, et al.
Alzheimers Dement
. 2016 Nov;
13(6):710-719.
PMID: 27870938
Introduction: Accurate diagnosis of prion diseases and discrimination from alternative dementias gain importance in the clinical routine, but partial overlap in cerebrospinal fluid (CSF) biomarkers impedes absolute discrimination in the...
20.
Kanata E, Arsenakis M, Sklaviadis T
Prion
. 2016 Aug;
10(5):391-408.
PMID: 27537339
Scrapie, the prion disease of sheep and goats, is a devastating malady of small ruminants. Due to its infectious nature, epidemic outbreaks may occur in flocks/herds consisting of highly susceptible...