Zobrazeno 1 - 10
of 42
pro vyhledávání: '"N L, Sheremet"'
Autor:
A. K. Kalashnikova, D. D. Eliseeva, N. A. Andreeva, N. V. Zhorzholadze, I. A. Ronzina, R. Ts. Bembeeva, N. N. Venediktova, M. R. Kalganova, N. L. Sheremet
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 16, Iss 3, Pp 52-57 (2024)
The discovery of antibodies against aquaporin-4 (AQP4) and against myelinoligodendrocyte glycoprotein (MOG) confirmed the existence of two disease entities distinct from multiple sclerosis (MS) — neuromyelitis optica spectrum disorders (NMOSD) and
Externí odkaz:
https://doaj.org/article/fd515cc5e10f4901936cdc4c615f82f4
Autor:
N. L. Sheremet, D. D. Eliseeva, V. V. Bryukhov, N. A. Andreeva, N. V. Zhorzholadze, Yu. K. Murakhovskaya, A. K. Kalashnikova, M. N. Zakharova
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 15, Iss 0, Pp 35-42 (2023)
Optic neuritis (ON) can often occur at the onset of a demyelinating autoimmune CNS disease or as one of its clinical manifestations. The introduction of novel laboratory techniques, technical advances in magnetic resonance imaging (MRI), electrophysi
Externí odkaz:
https://doaj.org/article/d61eef3ed1224fd9b78789cd5dc80416
Autor:
N. A. Andreeva, N. L. Sheremet
Publikováno v:
Oftalʹmologiâ, Vol 18, Iss 3S, Pp 753-757 (2021)
Leber’s hereditary optic neuropathy (LHON) is a maternal inherited mitochondrial disease characterized by bilateral vision loss in working age population. Although this pathology affects the retinal ganglion cells, the main manifestation of the dis
Externí odkaz:
https://doaj.org/article/272f641b8e9447feb9efc8e28a51fef7
Publikováno v:
Oftalʹmologiâ, Vol 18, Iss 3S, Pp 646-653 (2021)
The role of mitophagy in hereditary optic neuropathies is considering in this review. Mitochondria are intracellular double membrane organelles. They are one of the main components of all eukaryotic cells, they perform many different functions in the
Externí odkaz:
https://doaj.org/article/4a305d91188941b0b907f837bd90b054
Autor:
N. L. Sheremet, N. A. Andreeva, A. D. Meshkov, A. L. Chukhrova, A. N. Loginova, A. V. Polyakov
Publikováno v:
Сибирский научный медицинский журнал, Vol 38, Iss 5, Pp 25-31 (2019)
Purpose: to study the etiological structure and incidence rate of various genesis optical neuropathies (ON) according to the own observation data. Material and methods. The study is based on the data analysis from a survey of 658 patients (982 eyes)
Externí odkaz:
https://doaj.org/article/63b48076ccb94d09a544fd90c513c603
Autor:
N. L. Sheremet, I. G. Grushke, N. V. Zhorzholadze, I. A. Ronzina, A. A. Mikaelyan, S. A. Kurbatov, V. V. Kadyshev, K. I. Anoshkin, V. V. Strelnikov
Publikováno v:
Сибирский научный медицинский журнал, Vol 38, Iss 5, Pp 65-71 (2019)
Purpose of the study was to assess the spectrum of molecular genetic disorders and the variety of clinical forms in patients with Stargardt disease. Material and methods. 56 patients aged 15-44 years who had been diagnosed with Stargardt disease in a
Externí odkaz:
https://doaj.org/article/dd9051f9de144ecca4e63b03284bd4cb
Autor:
N L, Sheremet, N A, Andreeva, N V, Zhorzholadze, Yu K, Murakhovskaya, M S, Shmelkova, T D, Krylova, P G, Tsygankova
Publikováno v:
Vestnik oftalmologii. 138(4)
Folate metabolism disorders are known to have a potential involvement in the pathophysiology of mitochondrial diseases. Many researchers suggest that profound systemic folate deficiency may contribute to mitochondrial folate deficiency. Folic acid me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed7e546b78559580a662f899551bbf21
https://pubmed.ncbi.nlm.nih.gov/36004588
https://pubmed.ncbi.nlm.nih.gov/36004588
Autor:
T. D. Krylova, P. G. Tsygankova, Y. S. Itkis, N. L. Sheremet, T. A. Nevinitsyna, S. V. Mikhaylova, E. Y. Zakharova
Publikováno v:
Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry. 12:43-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e6e20532f1caebdda54334568dc12d8
https://doi.org/10.1134/s1990750818010080
https://doi.org/10.1134/s1990750818010080
Publikováno v:
Vestnik oftalmologii. 135(5. Vyp. 2)
Retinal diseases associated with damage to retinal pigment epithelium (PPE) are the most frequent causes of irreversible loss of vision in adults. Since there is no therapeutic treatment available that could repair RPE and its connections with the ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24970de06ced6785f1d9926f84c67a39
https://pubmed.ncbi.nlm.nih.gov/31691665
https://pubmed.ncbi.nlm.nih.gov/31691665
Autor:
N L Sheremet, N A Khanakova
Publikováno v:
Vestnik oftalmologii. 134(6)
To determine the causes and study the clinical manifestations of compressive optic neuropathy (CON).The study included 24 male and 36 female patients with CON (in total 60 patients, 97 eyes). All patients underwent standard ophthalmic examination, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e63af10ffd3a8e6223978c6e989063cb
https://pubmed.ncbi.nlm.nih.gov/30721204
https://pubmed.ncbi.nlm.nih.gov/30721204