Zobrazeno 1 - 10
of 280
pro vyhledávání: '"N A 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. Sheremet
Publikováno v:
Концепт: философия, религия, культура, Vol 6, Iss 3, Pp 68-82 (2022)
The article analyzes the intersection of universal and regional human rights concepts in Latin America. The regional approach to human rights protection has been proposed by anthropologists who argue that cultural relativism is the basis for the deve
Externí odkaz:
https://doaj.org/article/f691997bd976463ab8985280390051c6
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:
I. V. Markova, N. M. Sheremet
Publikováno v:
Научный вестник МГТУ ГА, Vol 24, Iss 1, Pp 42-48 (2021)
The modern tendencies in the Russian system of education, the emergence of competition and market relations in this sphere facilitated the reconsideration of the scientific grounds for the higher educational establishments activity. The suggested the
Externí odkaz:
https://doaj.org/article/69e5b36e40b24f93ba9b3e804f1a7e78
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:
D. K. Bekyashev, N. A. Sheremet
Publikováno v:
Kutafin Law Review. 10:179-198
Publikováno v:
Cosmic Research. 60:S27-S37