K V Baryshev,D V Petrachkov
K V Baryshev
This review addresses the problem of treating large-diameter full-thickness macular holes (FTMH). Surgical repair of FTMHs has been successfully performed since the late 20th century, however FTMHs with a diameter exceeding 500-600 µm, as ...
S V Yanchenko,B G Hamroev,A V Malyshev et al.
S V Yanchenko et al.
According to publications from 2016-2025, the prevalence of dry eye disease (DED) based on the assessment of clinical signs and symptoms in young and middle-aged adults may exceed 30.8-41.43%, while based on symptoms the prevalence ranges f...
Kh M Kamilov,A F Yusupov,M S Kasimova et al.
Kh M Kamilov et al.
Glaucoma remains one of the leading causes of irreversible vision loss, making it one of the most pressing problems in modern public health. Purpose: This...
[Experimental assessment of mass transfer in the human cornea using cesium ion migration as a model] [0.03%]
Yu Yusef,I A Novikov,G A Osipyan et al.
Yu Yusef et al.
The pathogenesis of endothelial corneal dystrophies involves disruption of the natural balance between fluid influx into and efflux from the corneal stroma. Regulation of fluid transport across the endothelial layer in vivo is primarily ass...
E V Boiko,V E Karev,A L Pozniak et al.
E V Boiko et al.
Chlamydial conjunctivitis accounts for 3 to 30% cases of conjunctivitis of various etiologies. In such patients, latent clinical manifestations do not correspond to morphological changes in the infected organs and tissues. This paper presen...
[Ciliary body medulloepithelioma associated with fungal endophthalmitis (clinical observation)] [0.03%]
I E Panova,E V Samkovich,A A Pimenova et al.
I E Panova et al.
This article presents two clinical cases of medulloepithelioma of the nonpigmented epithelium of the ciliary body, an extremely rare congenital intraocular tumor that may follow either a benign or malignant course. In the presented cases, l...
[Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 2. Clinical, social and demographic characteristics of inherited retinal pathologies] [0.03%]
V V Kadyshev,A A Stepanova,K K Shefer et al.
V V Kadyshev et al.
Purpose: The secondary objectives of the study were to describe the sociodemographic and clinical characteristics of patients with inherited retinal dystrophy (IRD) phenotypes, including Leber congenital amaurosis (LCA) a...
Multicenter Study
Vestnik oftalmologii. 2026;142(1):79-86. DOI:10.17116/oftalma202614201179 2026
[Results of the multicenter study "Registry of patients with inherited retinal dystrophies caused by confirmed biallelic mutations in the RPE65 and RLBP1 genes in Russia (REGINA)". Report 1. Molecular genetic characteristics of inherited retinal pathologies] [0.03%]
V V Kadyshev,A A Stepanova,K K Shefer et al.
V V Kadyshev et al.
Purpose: The primary objective of the study was to investigate and describe the molecular genetic characteristics of patients with inherited retinal dystrophies (IRDs) presenting with phenotypes of Leber congenital amauro...
Multicenter Study
Vestnik oftalmologii. 2026;142(1):70-78. DOI:10.17116/oftalma202614201170 2026
Yu A Huseva,M I Pazniak
Yu A Huseva
Purpose: This study aimed to investigate the morphological features of the lamina cribrosa (LC) of the scleral in terms of their potential role in optic nerve (ON) axonal injury. ...
D S Ismailova,P I Novikov,I V Zhitareva
D S Ismailova
Purpose: This study analyzed outcomes of orbital inflammation in granulomatosis with polyangiitis (GPA) and identified risk factors for unfavorable outcomes. ...