Zobrazeno 1 - 10
of 30
pro vyhledávání: '"T V Fedotova"'
Autor:
T V Fedotova
Publikováno v:
Russian journal of linguistics: Vestnik RUDN, Vol 0, Iss 3, Pp 84-93 (2009)
The article reveals the main factors that had an effect on peopling the territory of Eastern Transbaical. Migrants' conduct towards the existing toponymic system is analysed. An attempt to single out the characteristic features and the main groups of
Externí odkaz:
https://doaj.org/article/9f89c46ef70544ee86e60d3702745002
Autor:
T V Fedotova
Publikováno v:
Russian journal of linguistics: Vestnik RUDN, Vol 0, Iss 2, Pp 91-98 (2009)
The paper deals with the representation of the concept «space» according to the Zabaikalye region toponimic space data. The author comes to the conclusion that this concept is very important for the reconstruction of the East Zabaicalye first resid
Externí odkaz:
https://doaj.org/article/c293a063b42f44ecaa7b571adcb08cd3
Autor:
A. F. Murtazina, O. A. Shchagina, T. B. Milovidova, E. L. Dadali, G. E. Rudenskaya, S. A. Kurbatov, T. V. Fedotova, S. S. Nikitin, P. A. Sparber, M. D. Orlova, A. V. Polyakov
Publikováno v:
Нервно-мышечные болезни, Vol 10, Iss 2, Pp 39-45 (2020)
Introduction. Charcot–Marie–Tooth disease type 4D is a hereditary demyelinating neuropathy, that occurs with the high frequency in patients of Roma origin. It is characterized by early onset at the age of 2–10 years and hearing impairment, mani
Externí odkaz:
https://doaj.org/article/f0577b02099e4f6d8c46c8a3b3e02aca
Publikováno v:
Doklady Physical Chemistry. 508:17-21
Publikováno v:
Russian Chemical Bulletin. 71:199-211
Autor:
Yu. H. Boreiko, T. V. Fedotova
Publikováno v:
Perspectives. Socio-political journal. :71-77
Autor:
T. V. Fedotova
Publikováno v:
Вестник ВГУ Серия Лингвистика и межкультурная коммуникация. :42-49
Autor:
T. V. Fedotova, T. T. Cherkashina
Publikováno v:
Bulletin of the Moscow State Regional University (Russian philology). :32-41
Autor:
V. P. Fedotov, I. S. Kleimenova, T. V. Fedotova, D. S. Stepanov, E. A. Proskurina, E. Yu. Zakharova
Publikováno v:
Нервно-мышечные болезни, Vol 0, Iss 3, Pp 49-53 (2015)
Pompe disease (PD), or glycogen storage disease type II, is a rare autosomal recessive lysosomal disease caused by glycogen storage in the myocardium, skeletal muscles, and liver. PD, as an orphan disease with a very low prevalence rate, shows a mark
Externí odkaz:
https://doaj.org/article/ef82c62c2f9b46f0a34116d914ff7cb6
Publikováno v:
Russian Physics Journal. 63:1363-1369
The results of investigations of the properties of cyanine dye dimers in the triplet state are presented. The formation of dimers is demonstrated as two absorption bands of differing intensities, which are due to splitting of the S*-level of monomers