Zobrazeno 1 - 6
of 6
pro vyhledávání: '"N. Sh. Kokoeva"'
Autor:
L. V. Kogoleva, M. S. Ivanova, E. N. Demchenko, T. V. Sudovskaya, Ju. A. Bobrovskaya, N. Sh. Kokoeva, A. A. Makarova
Publikováno v:
Российский офтальмологический журнал, Vol 16, Iss 1, Pp 41-46 (2023)
Purpose: to analyze the clinical manifestations, course, and results of treatment of Coats disease in children. Materials and methods. We performed a retrospective analysis of medical records of 59 patients with Coats retinitis (83 % were boys) who h
Externí odkaz:
https://doaj.org/article/b7dd839542684299b5bd460b4a06c719
Autor:
I. V. Zolnikova, V. V. Kadyshev, A. V. Marakhonov, A. B. Chernyak, S. V. Milash, Yu. A. Bobrovskaya, N. A. Urakova, N. Sh. Kokoeva, S. I. Kutsev, R. A. Zinchenko
Publikováno v:
Oftalʹmologiâ, Vol 18, Iss 4, Pp 897-907 (2021)
Aim: to study genotype-phenotype correlations in patients with inherited retinal diseases with mutations in ABCA4 gene in Russian Federation.Patients and methods. 21 patients from Russian population aged from 7 to 51 years old (mean age 20 ± 11 year
Externí odkaz:
https://doaj.org/article/91590bec4d1f4f4ab2300d81ff5a86e4
Publikováno v:
Russian Pediatric Ophthalmology. 11:196-199
Objective. To evaluate the influence of the central corneal thickness on the characteristics of the ophthalmic tone in the children presenting with congenital microphthalmia of different severity and to describe its clinical significance for diagnost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::484adfa29548f619cf4f5a7ae6559151
https://doi.org/10.18821/1993-1859-2016-11-4-196-199
https://doi.org/10.18821/1993-1859-2016-11-4-196-199
Publikováno v:
Russian Pediatric Ophthalmology. 12:225-227
This article was designed to report the clinical case of ocular echinococcosis in a child. The patient was characterized by ptosis, oedema of the periorbital tissues, exophthalmos, displacement of the eye bulb, its abnormal movements in all direction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69619a34aae16365a6f5dbd957a75409
https://doi.org/10.18821/1993-1859-2017-12-4-225-227
https://doi.org/10.18821/1993-1859-2017-12-4-225-227
Publikováno v:
Russian Pediatric Ophthalmology. 12:163-165
This article was designed to report a clinical case of a rare syndromic disease - Pallister-Killians’s syndrome characterized by the signs of mental deficiency, abnormal features of cranial bones , congenitally reduced arterial pressure, multiple a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cd35924b4413e515db659c93fa72214
https://doi.org/10.18821/1993-1859-2017-12-3-163-165
https://doi.org/10.18821/1993-1859-2017-12-3-163-165
Publikováno v:
Vestnik oftalmologii. 132(3)
To develop a comprehensive classification system of distinctive clinical and anatomical features of congenital microphthalmia and anophthalmia in children and to specify indications, contraindications, and optimal timing of the primary and subsequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c78ecfed242b4f87463e602d1a8e532f
https://pubmed.ncbi.nlm.nih.gov/27456557
https://pubmed.ncbi.nlm.nih.gov/27456557