Zobrazeno 1 - 10
of 14
pro vyhledávání: '"A. V. Belodedova"'
Publikováno v:
Oftalʹmologiâ, Vol 20, Iss 1, Pp 95-104 (2023)
Purpose: to evaluate the clinical and functional results of two methods of Descemet’s membrane endothelial keratoplasty using a full and half graft.Patients and methods. This study is based on surgical treatment of 54 patients (54 eyes) with catara
Externí odkaz:
https://doaj.org/article/bad060b47a2945ce80a2baeffc8384ed
Autor:
L. O. Skorodumova, A. V. Belodedova, E. S. Zakharova, Е. I. Sharova, M. M. Bikbov, E. L. Usubov, O. P. Antonova, B. E. Malyugin
Publikováno v:
Офтальмохирургия, Vol 0, Iss 1, Pp 6-13 (2020)
Purpose. To assess an association of markers near the COL5A1 gene and in its intron with keratoconus. To study the relationship between the presence of marker alleles and the level of expression of the COL5A1 gene in the cornea of patients with kerat
Externí odkaz:
https://doaj.org/article/8ca6c1a3087d49b4997463cd590bcf71
Autor:
Liubov O. Skorodumova, Alexandra V. Belodedova, Elena I. Sharova, Elena S. Zakharova, Liliia N. Iulmetova, Mukharram M. Bikbov, Emin L. Usubov, Olga P. Antonova, Oksana V. Selezneva, Anastasia Levchenko, Olga Yu Fedorenko, Svetlana A. Ivanova, Raul R. Gainetdinov, Boris E. Malyugin
Publikováno v:
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Keratoconus is a chronic degenerative disorder of the cornea characterized by thinning and cone-shaped protrusions. Although genetic factors play a key role in keratoconus development, the etiology is still under investigation. Th
Externí odkaz:
https://doaj.org/article/51a073b678084fc7bac978342a369563
Autor:
Mukharram M. Bikbov, Oksana V. Selezneva, E. L. Usubov, Liubov O. Skorodumova, Olga P. Antonova, Olga Yu Fedorenko, Anastasia Levchenko, Liliia N. Iulmetova, Elena S. Zakharova, Svetlana A. Ivanova, Alexandra V. Belodedova, Boris Malyugin, Raul R. Gainetdinov, Elena I. Sharova
Publikováno v:
BMC Ophthalmology
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-9 (2021)
Background Keratoconus is a chronic degenerative disorder of the cornea characterized by thinning and cone-shaped protrusions. Although genetic factors play a key role in keratoconus development, the etiology is still under investigation. The occurre
Publikováno v:
Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry. 13:214-227
Keratoconus is a chronic disorder of the cornea, characterized by its progressive thinning, stretching, and conical protrusion. Diagnostics of subclinical keratoconus, as well as its early stages (forme fruste), is a complex problem. The presence of
Autor:
A V Shatskikh, M M Jones, E V Kovshun, A V Belodedova, A V Enkina, A.V. Golovin, D.S. Ostrovsky, S A Borzenok, B E Malyugin
Publikováno v:
Vestnik oftalmologii. 136(5)
To evaluate biocompatibility of the new keratoprosthesis supporting plates (KSP) in rabbitsThe study included 15 chinchilla rabbits. In the first group (5 rabbit eyes) KSP made of hydrophobic acryl with square penetrating holes of 220×220 micron (mo
Autor:
Boris Malyugin, Vladimir A. Veselovsky, Olga P. Antonova, Liubov O. Skorodumova, E. I. Sharova, Andrey K. Larin, Alexandra V. Belodedova, Anastasia S. Nikitina, E. S. Kostryukova
Publikováno v:
Data in Brief, Vol 25, Iss, Pp-(2019)
Fuchs endothelial corneal dystrophy (FECD) is a bilateral inherited eye disease with advanced forms only treatable by corneal transplantation. The pathogenesis of FECD has not been worked out yet, however, trinucleotide repeat polymorphism CTG18.1 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5000ffeb51e71cb25cccea556122859c
https://europepmc.org/articles/PMC6558234/
https://europepmc.org/articles/PMC6558234/
Autor:
Oksana V. Selezneva, Alexandra V. Belodedova, Olga P. Antonova, Tatiana A Akopian, Liubov O. Skorodumova, E. I. Sharova, Boris Malyugin, Elena S. Kostryukova
Publikováno v:
Investigative Opthalmology & Visual Science. 59:4748
Purpose To assess the occurrence and diagnostic performance of nine single-nucleotide variants (SNVs) in the TCF4, SLC4A11, LOXHD1, and AGBL1 genes and the CTG18.1 trinucleotide repeat expansion in a Russian cohort of Fuchs' endothelial corneal dystr
Publikováno v:
Laboratornoe delo. (4)
Autor:
R. G. Melik-Orandzhanyan, E. P. Studentsov, N. A. Smorygo, V. S. Mirzoyan, B. A. Ivin, Zh. V. Belodedova
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:538-545
5-Arylazo and 5-arylideneamino-2,4,6-triaminopyrimidines and their 6-hydroxy analogs were obtained by azo coupling of 2,4,6-triamino- and 2,4-diamino-6-hydroxypyrimidines with aryldiazonium salts, and also by the reaction of benzaldehydes with 2,4,5,