Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Sheremet NL"'
Publikováno v:
Vestnik oftalmologii. 137(5)
Unilateral pigmentary retinopathy (PR) is a rare, atypical form of hereditary retinal pathology. Different types of secondary retinopathy associated with various non-hereditary diseases, trauma or intoxication can imitate unilateral PR. Therefore, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e78cc4c32b4f6b9657706c4735893291
https://pubmed.ncbi.nlm.nih.gov/34726865
https://pubmed.ncbi.nlm.nih.gov/34726865
Publikováno v:
Vestnik oftalmologii. 137(1)
To simulate the damaging effect on retinal pigment epithelium (RPE) in an experiment studying the effect of human neuronal precursors (NPs).The study was carried out on 31 rabbits (31 eyes) of the Chinchilla breed, which were divided into 3 groups: t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c876ec5b86f2cc8022f905056dd1172c
https://pubmed.ncbi.nlm.nih.gov/33610143
https://pubmed.ncbi.nlm.nih.gov/33610143
Publikováno v:
Vestnik oftalmologii. 136(4. Vyp. 2)
To identify the specifics of structural and functional changes in patients with toxic optical neuropathy caused by acute methanol poisoning.One female patient with toxic optic neuropathy (TON), 2 male patients with partial optic atrophy caused by met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed7fecad262ef55825d9e8b4caeffd3
https://pubmed.ncbi.nlm.nih.gov/32880146
https://pubmed.ncbi.nlm.nih.gov/32880146
Autor:
M.S. Shmelkova, Sheremet Nl, N V Zhorzholadze, N.A. Andreeva, T.D. Krylova, A V Fomin, P.G. Tsygankova
Publikováno v:
Vestnik oftalmologii. 136(4. Vyp. 2)
To investigate the features of various parameters of the density of retinal blood vessels, optic nerve head (ONH) and peripapillary region in hereditary optic neuropathy (HON) patients revealed with optical coherence tomography angiography (OCTA).The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4dde54b62dad79e911106eb43321dce
https://pubmed.ncbi.nlm.nih.gov/32880137
https://pubmed.ncbi.nlm.nih.gov/32880137
Publikováno v:
Vestnik oftalmologii. 136(4. Vyp. 2)
To evaluate the relationship between the morphological and functional parameters of retinal pigment epithelium (RPE) and photoreceptors (PR) in inherited retinal diseases (IRD).The study included 52 patients (104 eyes), 23 of them with Stargardt Dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a14025bed7deb98c08c4787cdbfe23e
https://pubmed.ncbi.nlm.nih.gov/32880138
https://pubmed.ncbi.nlm.nih.gov/32880138
Autor:
N V Zhorzholadze, I.G. Grushke, Alexander S Tanas, A.A. Mikaelyan, Sheremet Nl, Vladimir V Strelnikov, I.A. Ronzina
Publikováno v:
Vestnik oftalmologii. 134(6)
ABCA4 is one of the main genes whose mutations are associated with various inherited retinal diseases (IRD) such as Stargardt disease, cone dystrophy, cone-rod dystrophy, and retinitis pigmentosa. The severity of retinal dystrophy phenotype may be re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::625cf37c2668a37314a539dcbad215ce
https://pubmed.ncbi.nlm.nih.gov/30721205
https://pubmed.ncbi.nlm.nih.gov/30721205
Publikováno v:
Vestnik oftal'mologii. 136:333
Stargardt disease is a hereditary retinal dystrophy associated with mutations in the ABCA4 gene. Currently, no etiopathogenetic drugs nor treatment methods for Stargardt disease have completely passed clinical trials. The review summarizes experiment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fba95d67f1c55426239b4a3666ba35ba
https://doi.org/10.17116/oftalma2020136042333
https://doi.org/10.17116/oftalma2020136042333
Publikováno v:
Vestnik oftalmologii. 134(4)
ABCA4 is one of the main genes which mutations are associated with various inherited retinal diseases (IRD) such as Stargardt disease, cone dystrophy, cone-rod dystrophy, and retinitis pigmentosa. Wide prevalence of IRD, high heterogeneity of ABCA4 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba33a233b81b09eae19ba80362c5a8ec
https://pubmed.ncbi.nlm.nih.gov/30166513
https://pubmed.ncbi.nlm.nih.gov/30166513
Autor:
T B Smirnova, N A Khanakova, Sheremet Nl, A D Meshkov, N L Kozlovskaya, V.M. Sheludchenko, I.A. Ronzina
Publikováno v:
Vestnik oftalmologii. 133(6)
to analyze the structure, risk factors, and causes of ischemic optic neuropathy (ION).A total of 239 patients (303 eyes) with ION and 98 patients (185 eyes) with optic disc drusen were examined. All ION patients underwent general clinical assessment.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::936e98f5db1b0ef7d1957e6dc2a6b494
https://pubmed.ncbi.nlm.nih.gov/29319669
https://pubmed.ncbi.nlm.nih.gov/29319669
Autor:
A N Loginova, Vladimir V Strelnikov, Sheremet Nl, A L Chukhrova, I.A. Ronzina, N V Zhorzholadze, I.G. Grushke, A. V. Polyakov, P. O. Shcherbakova, Alexander S Tanas, S. A. Kurbatov
Publikováno v:
Vestnik oftalmologii. 133(4)
To comparatively evaluate the efficacy of genetic screening in patients with Stargardt disease (SD) by using an express panel of 5 most common ABCA4 mutations and performing massive parallel sequencing of all coding regions of the ABCA4, ELOVL4, PROM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeaefb4917a58149d046b1ef397dad12
https://pubmed.ncbi.nlm.nih.gov/28980559
https://pubmed.ncbi.nlm.nih.gov/28980559