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N L Sheremet

Showing results (51-60 of 72) with videos related to

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Vestnik Oftalmologii|November 23, 2013
[Experimental study of the influence of disturbing factors and chaperone-like drugs on cataractogenesis]S E Avetisov, N L Sheremet, K O Muranov, et al.
Vestnik Oftalmologii|July 2, 2013
[Clinical and molecular genetic analysis of hereditary optic neuropathies]S É Avetisov, N L Sheremet, O K Vorob'eva, et al.
Vestnik Oftalmologii|May 21, 2008
[Search for chaperon-like anticataract agents, the antiaggregants of lens crystallin. Communication 3. Possibilities of a follow-up of caractogenesis processes on a prolonged rat model of UV-induced cataract]S E Avetisov, G S Polunin, N L Sheremet, et al.
Vestnik Oftalmologii|June 30, 2012
[Experimental study of influence of different damaging factors on lens. Report 1. Features of biomicroscopic changes]N L Sheremet, K O Muranov, N B Polianskiĭ, et al.
Vestnik Oftalmologii|June 30, 2012
[Experimental study of influence of different damaging factors on lens. Report 3. Changes of lens protein composition]V S Kurova, K O Muranov, N B Polianskiĭ, et al.
Vestnik Oftalmologii|June 30, 2012
[Experimental study of influence of different damaging factors on lens. Report 2. Features of microscopic lens changes]K O Muranov, N B Polianskiĭ, K I Bannik, 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|December 15, 2011
[The value of autofluorescence imaging in diagnosis of retinal diseases]S É Avetisov, T N Kiseleva, M V Vorob'eva, et al.
Vestnik Oftalmologii|October 22, 2013
[Peculiarities of ocular blood flow in ischemic optic neuropathy and normal tension glaucoma]V R Mamikonian, N S Galoian, 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.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Vestnik Oftalmologii|November 23, 2013
[Experimental study of the influence of disturbing factors and chaperone-like drugs on cataractogenesis]S E Avetisov, N L Sheremet, K O Muranov, et al.
Vestnik Oftalmologii|July 2, 2013
[Clinical and molecular genetic analysis of hereditary optic neuropathies]S É Avetisov, N L Sheremet, O K Vorob'eva, et al.
Vestnik Oftalmologii|May 21, 2008
[Search for chaperon-like anticataract agents, the antiaggregants of lens crystallin. Communication 3. Possibilities of a follow-up of caractogenesis processes on a prolonged rat model of UV-induced cataract]S E Avetisov, G S Polunin, N L Sheremet, et al.
Vestnik Oftalmologii|June 30, 2012
[Experimental study of influence of different damaging factors on lens. Report 1. Features of biomicroscopic changes]N L Sheremet, K O Muranov, N B Polianskiĭ, et al.
Vestnik Oftalmologii|June 30, 2012
[Experimental study of influence of different damaging factors on lens. Report 3. Changes of lens protein composition]V S Kurova, K O Muranov, N B Polianskiĭ, et al.
Vestnik Oftalmologii|June 30, 2012
[Experimental study of influence of different damaging factors on lens. Report 2. Features of microscopic lens changes]K O Muranov, N B Polianskiĭ, K I Bannik, 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|December 15, 2011
[The value of autofluorescence imaging in diagnosis of retinal diseases]S É Avetisov, T N Kiseleva, M V Vorob'eva, et al.
Vestnik Oftalmologii|October 22, 2013
[Peculiarities of ocular blood flow in ischemic optic neuropathy and normal tension glaucoma]V R Mamikonian, N S Galoian, 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.
Pageof 8