Zobrazeno 1 - 10
of 10
pro vyhledávání: '"L P, Balashova"'
Autor:
N. A. Bakunina, L. M. Balashova
Publikováno v:
Российский офтальмологический журнал, Vol 16, Iss 3, Pp 118-126 (2023)
Purpose: to clarify the pathogenetic classification of primary angle-closure glaucoma (PACG) based on genetic studies and retrospective analysis.Material and methods. 28 patients (44 eyes) aged 40 to 75 years with various forms of initial, advanced,
Externí odkaz:
https://doaj.org/article/3de8a31f44cc414c81b6fdc6c6ac6127
Publikováno v:
Российский офтальмологический журнал, Vol 16, Iss 2, Pp 113-118 (2023)
Purpose: clinical and genetic research of primary chronic angle-closure glaucoma (PACG) and age-related macular degeneration (AMD) for prospective pathogenetically-oriented targeted treatment of these condition.Materials and methods. 15 patients with
Externí odkaz:
https://doaj.org/article/55d90fc93a1b4b0c9ce8035dea577106
Publikováno v:
Российский офтальмологический журнал, Vol 14, Iss 4, Pp 22-30 (2022)
Purpose. To study the involvement of vascular and vegetative factors in the pathogenesis of glaucoma attack. Material and methods. 12 patients (24 eyes) aged 49 to 82 — 5 men and 7 women, including 3 patients with acute glaucoma and 9 patients with
Externí odkaz:
https://doaj.org/article/3d20c3ee92ed4f7784b6be482982820d
Publikováno v:
Oftalʹmologiâ, Vol 18, Iss 4, Pp 885-896 (2021)
Purpose. To study the effectiveness of vascular, anti-inflammatory and fibrinolytic therapy, to conduct a comparative assessment with treatment without vascular therapy in patients with angle-closure (ACG) and mixed glaucoma.Methods. A total of 55 pa
Externí odkaz:
https://doaj.org/article/cbb0b2fc1c1c4f33a707f42e8a34f15b
Autor:
M. E. Weener, D. S. Atarshchikov, V. V. Kadyshev, I. V. Zolnikova, A. M. Demchinsky, D. Barh, L. M. Balashova, J. M. Salmasi
Publikováno v:
Российский офтальмологический журнал, Vol 14, Iss 1, Pp 80-88 (2021)
This literature review offers a detailed description of the genes and proteins involved in pathophysiological processes in isolated retinitis pigmentosa (RP). To date, 84 genes and 7 candidate genes have been described for non-syndromic RP. Each of t
Externí odkaz:
https://doaj.org/article/859c3bbf08444417af37921d6045973e
Autor:
M. E. Ivanova, I. V. Zolnikova, I. E. Khatsenko, V. V. Strelnikov, F. A. Konovalov, E. R. Lozier, M. A. Ampleeva, A. V. Antonets, I. V. Kanivets, K. V. Gorgisheli, D. S. Atarshchikov, D. V. Pyankov, S. A. Korostelev, E. B. Kuznetsova, D. Bar, L. M. Balashova, Zh. M. Salmasi
Publikováno v:
Российский офтальмологический журнал, Vol 13, Iss 1, Pp 12-22 (2020)
Achromatopsia (ACHM) is a rare autosomal recessive disease. Its mutation spectrum is well described in other populations, but the data on ACHM prevalence and features in Russia are insufficient. Purpose. To describe clinically and genetically the Rus
Externí odkaz:
https://doaj.org/article/92260456696c478c91e15c42a02ce1d3
Publikováno v:
Российский офтальмологический журнал, Vol 13, Iss 1, Pp 7-11 (2020)
Objective: to assess the effectiveness of tear substitutes in patients suffering from dry eye syndrome (DES). Material and methods. 100 patients with an established diagnosis of mild to moderate DES, averagely aged 42.0 ± 2.1, were divided into thre
Externí odkaz:
https://doaj.org/article/2401618df93b4037ba40e1c90eca20fe
Autor:
M. E. Ivanova, K. V. Gorgisheli, I. V. Zolnikova, D. S. Atarshchikov, D. Barh, Zh. M. Salmasi, L. M. Balashova
Publikováno v:
Российский офтальмологический журнал, Vol 12, Iss 3, Pp 77-84 (2019)
The complete form of X-linked congenital stationary night blindness (CSNB) is a rare genetic disease caused by a mutation in the NYX gene. CSNB is associated with the mutations taking place in 17 genes, whilst its CSNB1A form is caused by the mutatio
Externí odkaz:
https://doaj.org/article/01aeb942b8a8469a9671f5327953e5ec
Autor:
L. M. Balashova, Y. D. Kuznetsova, L. S. Korobova, E. P. Kantarzhi, V. E. Mukhin, E. A. Cherkashina, S. N. Bykovskaya
Publikováno v:
Российский офтальмологический журнал, Vol 12, Iss 2, Pp 5-11 (2019)
Purpose: to study the role of cellular immunity in the development of retinopathy of prematurity (ROP).Material and methods. 87 children were tested, including 60 with III — V stage ROP and posterior aggressive retinopathy that had gestational age
Externí odkaz:
https://doaj.org/article/f9147233f9f848c583ecb419b05ac454
Publikováno v:
Vrachebnoe delo. (11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a28e4dc96a78d795bec96be761fb6e6
https://pubmed.ncbi.nlm.nih.gov/1199062
https://pubmed.ncbi.nlm.nih.gov/1199062