Showing results (21-30 of 30) with videos related to
Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Vestnik Oftalmologii|September 4, 2020
[Morphological and functional indicators of retinal pigment epithelium and photoreceptor apparatus in inherited retinal diseases]N L Sheremet, I A Ronzina, A A Mikaelyan, et al.Vestnik Oftalmologii|January 26, 2017
[Electrophysiological parameters of the retina in idiopathic macular hole]I A Ronzina, S V Sdobnikova, V M Sheludchenko, et al.Vestnik Oftalmologii|November 23, 2013
[Field of view changes after vitreomacular surgery: a treatment quality criteria]S V Sdobnikova, I V Kozlova, E V Doroshenko, et al.Vestnik Oftalmologii|January 11, 2018
[Analysis of structure, causes, and risk factors of ischemic optic neuro-pathy]N L Sheremet, T B Smirnova, I A Ronzina, et al.Vestnik Oftalmologii|February 6, 2019
[Clinical polymorphism of splice site mutations in the ABCA4 gene]N L Sheremet, I G Grushke, N V Zhorzholadze, et al.Vestnik Oftalmologii|May 29, 2014
[Stargardt's disease and abiotrophy of Franceschetti (fundus flavimaculatus): pathogenetic, clinical, and molecular genetic characteristics]M T Bondarenko, N V Zhorzholadze, N L Sheremet, et al.Vestnik Oftalmologii|October 2, 2019
[Phenotype-genotype correlations in patients with inherited retinal diseases with p.G1961E mutation in the ABCA4 gene]N L Sheremet, I G Grushke, N V Zhorzholadze, et al.Vestnik Oftalmologii|October 6, 2017
[Molecular genetic diagnosis of Stargardt disease]N L Sheremet, N V Zhorzholadze, I A Ronzina, et al.Vestnik Oftalmologii|April 30, 2022
[Electrophysiological and psychophysical studies in assessment of visual functions in patients with hereditary optic neuropathy]N L Sheremet, I A Ronzina, N A Andreeva, et al.Biochemistry. Biokhimiia|July 25, 2016
Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber's Hereditary Optic NeuropathyN L Sheremet, T A Nevinitsyna, N V Zhorzholadze, et al.Pageof 3