Zobrazeno 1 - 10
of 46
pro vyhledávání: '"A Kaminioti"'
Autor:
A Liozidou, A Karamplianis, A Kaminioti, I Sakalidou, E Poulimenou, A Papadimitriou, D Papadimitriou
Publikováno v:
Dialogues in Clinical Neuroscience & Mental Health, Vol 1, Iss s3 (2018)
A 46-year-old woman presented with acute onset diplopia, opthalmoparesis, confusion and gait instability. She had a positive history for probable Multiple Sclerosis (MS), depression and alcohol use. During the hospitalization she progressively develo
Externí odkaz:
https://doaj.org/article/8cff6be9436949eea4613e6bd96eff49
INTRODUCTION: Fragile X Syndrome (FXS) is an X-chromosome linked, neurodevelopmental disorder, which is caused by the silencing of the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene that encodes the Fragile X Messenger Ribonucleoprotein (FMRP) p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______463::c501f560a464413664ff674c263bddcf
https://hdl.handle.net/1842/40651
https://hdl.handle.net/1842/40651
Publikováno v:
Circular Economy and Sustainability. 2:383-399
Publikováno v:
Education + Training, 2005, Vol. 47, Issue 6, pp. 432-446.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/00400910510617051
Autor:
Catherine M. Abbott, Laura Kaminioti-Dumont, Colin Smith, Josephine MacDonald, Faith C. J. Davies, Jilly E Hope, Francis Nunez, Grant F. Marshall, Fiona McLachlan, Owen Dando, Oliver Hardt, Vesa Qarkaxhija, Emma R. Wood
Publikováno v:
Davies, F C J, Hope, J E, McLachlan, F, Marshall, G F, Kaminioti-Dumont, L, Qarkaxhija, V, Nunez, F, Dando, O, Smith, C, Wood, E, MacDonald, J, Hardt, O & Abbott, C M 2020, ' Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function ', Human Molecular Genetics, vol. 29, no. 10, pp. 1592–1606 . https://doi.org/10.1093/hmg/ddaa042
Heterozygous de novo mutations in EEF1A2, encoding the tissue-specific translation elongation factor eEF1A2, have been shown to cause neurodevelopmental disorders including often severe epilepsy and intellectual disability. The mutational profile is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eb98cc3db8d61e13a59849f9e042664
https://www.pure.ed.ac.uk/ws/files/138719673/D252H_paper_clean_manuscript_plus_figs.pdf
https://www.pure.ed.ac.uk/ws/files/138719673/D252H_paper_clean_manuscript_plus_figs.pdf
Akademický článek
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Autor:
Athanasia Karina, Gerasimos S. Armatas, Stella Fountoulaki, Ioannis Tamiolakis, Theodoros S. Symeonidis, Petros Gkizis, Ioannis N. Lykakis, Eleni Kaminioti
Publikováno v:
Advanced Synthesis & Catalysis. 358:1500-1508
In this article, the catalytic activity of titania-supported gold nanoparticles (Au/TiO2) was studied for the selective oxidation of amines into nitroso compounds using hydrogen peroxide (H2O2). Gold nanoparticles deposited on Degussa P25 polymorphs
Autor:
Matsota, Paraskevi1 matsota@yahoo.gr, Kaminioti, Eva1 evakaminiotis@gmail.com, Kostopanagiotou, Georgia1 banesthclin@attikonhospital.gr
Publikováno v:
BioMed Research International. 6/16/2015, Vol. 2015, p1-9. 9p.