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pro vyhledávání: '"P. P. Kanivets"'
Autor:
P. P. Kanivets
Publikováno v:
Вісник Харківського національного університету внутрішніх справ, Vol 103, Iss 4, Pp 197-206 (2023)
The main identification tasks of the commodity expertise of natural honey are to establish its authenticity, quality and assessment of compliance with the requirements of standards. To achieve these objectives, experts conduct a number of analyses an
Externí odkaz:
https://doaj.org/article/e390333a0e614f0192368843d5b92217
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Publikováno v:
Educational Technology Quarterly, Vol 2022, Iss 4 (2022)
The use of virtual teaching aids with AR technology in various areas of education, including physics, has been studied. The similarity between physical and electrical models has been established, and the development of a mobile app for studying simpl
Externí odkaz:
https://doaj.org/article/7873db04bc364b6097c62722bd3c8d95
Publikováno v:
Zaporožskij Medicinskij Žurnal, Vol 24, Iss 1, Pp 5-12 (2022)
The aim of the study was to investigate circulating miRNAs-27a, -221 levels and their correlations with lipid indices in patients with ischemic heart disease (IHD) and type 2 diabetes mellitus. Materials and methods. The study included 58 patients
Externí odkaz:
https://doaj.org/article/109d942b258d46d7a3fa2073755d83ed
Autor:
T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, M. Yu. Shorina, I. F. Demenshin, G. G. Prokopiev, I. V. Kanivets, V. S. Suchorukov, P. L. Anufriev, T. I. Baranich, A. A. Kozina, A. G. Prityko
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 3, Pp 51-63 (2021)
Congenital muscular dystrophies are heterogeneous groups of neuromuscular diseases leading to hypotonia, progressive muscle weakness and dystrophic or structural signs in muscle biopsy. At the present time, 34 genes associated with congenital muscula
Externí odkaz:
https://doaj.org/article/01099aa7c969436698e9e63a4c653882
Autor:
S. V. Mikhailova, E. V. Saifullina, P. V. Baranova, V. P. Vorontsova, D. I. Gribov, M. V. Zhivihina, A. N. Slatetskaya, R. V. Magzhanov, V. A. Samokhvalov, M. N. Virtseva, L. P. Borscheva, E. E. Koh, M. V. Novikova, A. V. Abrukova, E. Yu. Belyashova, N. Yu. Gerasimenko, L. V. Guseva, Zh. V. Yukhimenko, N. V. Nikitina, T. I. Belyaeva, T. A. Shkurko, N. A. Pichkur, V. S. Kakaulina, N. L. Pechatnikova, N . A. Polyakova, S. A. Korostelev, D. V. Pyankov, I. V. Kanivets, N. A. Demina, E. Yu. Pyrkova, G. V. Baidakova, M. V. Kurkina, E. Yu. Zakharova
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 2, Pp 61-79 (2021)
Background. Glutaric aciduria type 1 is an autosomal recessive disease caused by mutations in the GCDH gene, which encodes the enzyme glutaryl‑CoA dehydrogenase. Metabolic crisis in type 1 glutaric aciduria is an acute life‑threatening condition
Externí odkaz:
https://doaj.org/article/7260ea8a4de74abc9f7f0ad19298c84e
Clinical and genetic characteristics of distal arthrogryposis caused by mutations in the PIEZO2 gene
Autor:
T. V. Markova, E. L. Dadali, S. S. Nikitin, A. F . Murtazina, O. L. Mironovich, I. V. Kanivets
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 2, Pp 48-55 (2021)
Mutations in the PIEZO2 gene, which is involved in the formation of the mechanosensitive cation channel Piezo2, can cause distal arthrogryposis type 3 (Gordon’s syndrome), type 5, and Marden–Walker syndrome. Clinical and genetic characteristics o
Externí odkaz:
https://doaj.org/article/7b02dadbbcc84e028d1b72a97d5240b0
Publikováno v:
Русский журнал детской неврологии, Vol 15, Iss 3-4, Pp 65-77 (2021)
The review provides an analysis of 73 full-text articles, the source of which was the Medline, OMIM, NCBI, Pubmed, Scopus, eLibrary.ru databases. The data of studies of the main pathogenetic mechanisms of the formation of the cerebral palsy (CP) phen
Externí odkaz:
https://doaj.org/article/e899d1a5f9844c90af3c5bd2be2a37f2
Akademický článek
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