Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Georgia G. Yioti"'
Autor:
Georgios Vartholomatos, Maria Stefaniotou, Georgia G. Yioti, Orestis A. Panagiotou, Nikolaos I. Kolaitis, Evangelos Evangelou, Chrisavgi Pappa
Publikováno v:
Ophthalmic Genetics. 34:130-139
The genetic background of retinal vein occlusion (RVO) remains unclear. In the current study, we aimed to replicate polymorphisms related to thrombophilia/hypofibrinolysis in a Greek population and also systematically summarize current evidence avail
Autor:
Francis L. Munier, Georgia G. Yioti, Carel B. Hoyng, Pietro Farinelli, Sara Balzano, Jamie M Ellingford, Viet H. Tran, Olivier Bonny, Christos Ikonomidis, Sten Andréasson, Veronika Vaclavik, Chris F. Inglehearn, Nicola Bedoni, Lonneke Haer-Wigman, Daniel F. Schorderet, Maria Stefaniotou, Fabien Murisier, Adam P. Booth, Mohammed E El-Asrag, Carlo Rivolta, Konstantinos Nikopoulos, Nathalie M. Bax, Yan Litzistorf, Frans P.M. Cremers, Carmel Toomes, Beryl Royer-Bertrand, Graeme C.M. Black, Caroline C W Klaver, Martin McKibbin, Manir Ali, Alberta A H J Thiadens
Publikováno v:
Human Molecular Genetics, 25, 4546-4555
Scopus-Elsevier
Human Molecular Genetics, 25(20), 4546-4555. Oxford University Press
Human molecular genetics, vol. 25, no. 20, pp. 4546-4555
Human Molecular Genetics, 25, 20, pp. 4546-4555
Scopus-Elsevier
Human Molecular Genetics, 25(20), 4546-4555. Oxford University Press
Human molecular genetics, vol. 25, no. 20, pp. 4546-4555
Human Molecular Genetics, 25, 20, pp. 4546-4555
Hereditary retinal degenerations encompass a group of genetic diseases characterized by extreme clinical variability. Following next-generation sequencing and autozygome-based screening of patients presenting with a peculiar, recessive form of cone-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86735e0d0550260dadf7eb91ef7e54b7
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 43
BACKGROUND AND OBJECTIVE: To investigate the morphological substrate of the changes in visual function in eyes with retinitis pigmentosa and good visual acuity using spectral-domain optical coherence tomography (SD-OCT). PATIENTS AND METHODS: A total
Autor:
Yioti, Georgia G.1 (AUTHOR) gyioti@yahoo.com, Panagiotou, Orestis A.2 (AUTHOR), Vartholomatos, Georgios A.3 (AUTHOR), Kolaitis, Nikolaos I.3 (AUTHOR), Pappa, Chrisavgi N.1 (AUTHOR), Evangelou, Evangelos2 (AUTHOR), Stefaniotou, Maria I.1 (AUTHOR) mstefani@cc.uoi.gr
Publikováno v:
Ophthalmic Genetics. Sep2013, Vol. 34 Issue 3, p130-139. 10p.