Zobrazeno 1 - 7
of 7
pro vyhledávání: '"D S Atarshchikov"'
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
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
Publikováno v:
Терапевтический архив, Vol 87, Iss 10, Pp 42-49 (2015)
Aim. To implement in 2009—2012 the RESULT observational program on the use of insulin glargine (Lantus) in combination with insulin glulisine (Apidra) as a basal-bolus regimen in patients with type 1 diabetes mellitus (DM) to evaluate the efficienc
Externí odkaz:
https://doaj.org/article/ef7d9c95ddd243039e3f28f5fe344458
Publikováno v:
Problems of Endocrinology. 59:3-8
The present study included a total of 22 patients (44 eyes/orbits) presenting with endocrine ophthalmopathy (EOP) and Graves' disease. All of them underwent routine ophthalmological examination. The activity and severity of EOP were verified in accor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca1b94581afd38b51bf1151c386f0d8
https://doi.org/10.14341/probl20135953-8
https://doi.org/10.14341/probl20135953-8
Autor:
D. S. Atarshchikov, A. V. Ilyin, N. V. Efremova, O. N. Bondarenko, Marina Vladimirovna Shestakova, L L Bolotskaya
Publikováno v:
Europe PubMed Central
Терапевтический архив, Vol 87, Iss 10, Pp 42-49 (2015)
Терапевтический архив, Vol 87, Iss 10, Pp 42-49 (2015)
To implement in 2009-2012 the RESULT observational program on the use of insulin glargine (Lantus) in combination with insulin glulisine (Apidra) as a basal-bolus regimen in patients with type 1 diabetes mellitus (DM) to evaluate the efficiency and s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d437c2517cbb9a0113369b957fa2fe56
http://europepmc.org/abstract/med/26978173
http://europepmc.org/abstract/med/26978173
Publikováno v:
European Journal of Ophthalmology; 2012, Vol. 22 Issue 3, p515-529, 15p