Zobrazeno 1 - 10 of 397 pro vyhledávání: '"T A, Fedotova"'
1
Akademický článek
Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia
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
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5
REPRESENTATION OF THE CONCEPT OF «SPACE» IN THE ERGONYMIC SPACE OF KUBAN
Autor: T. V. Fedotova
Publikováno v: Вестник ВГУ Серия Лингвистика и межкультурная коммуникация. :42-49
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::41b7eb9db45c4c40a42403bcb30826f2
https://doi.org/10.17308/lk/1680-5755/2022/4a42-49
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7
Akademický článek
Infantile-onset Pompe disease (the first case diagnosed in Voronezh)
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
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8
Akademický článek
BASIC ASPECTS OF DEVELOPMENT OF CHRONIC IMMUNE DEFICIENCY AND/OR IMMUNOPATHOLOGY IN THE CHILDREN AND ADOLESCENTS
Autor: T. A. Fedotova, A. A. Mikhailenko, S. F. Sergeeva
Publikováno v: Медицинская иммунология, Vol 8, Iss 1, Pp 101-104 (2014)
Abstract. Analysis of clinical and anamnestic findings has been performed for 105 children 2 to 6 years old, and 101 adolescents 10-12 years old has been performed. Clinico-anamnestic data of children and addescents with and without chronic diseases
Externí odkaz: https://doaj.org/article/603bad85b38c4a21b1411f14d9468952
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9
Triplet States of Cyanine Dye Dimers
Autor: G. V. Zakharova, T. V. Fedotova, Alexander K. Chibisov, V. G. Plotnikov, Michael V. Alfimov
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f287c8d467d49321d5211ba27abc57d9
https://doi.org/10.1007/s11182-020-02179-0
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10
Clinical and genetic characteristics of Charcot–Marie–Tooth disease type 4D (type Lom) in Russia
Autor: Aysylu F. Murtazina, S. S. Nikitin, Peter Sparber, S. A. Kurbatov, A. V. Polyakov, M. D. Orlova, G. E. Rudenskaya, T. B. Milovidova, Elena L. Dadali, T. V. Fedotova, O. A. Shchagina
Publikováno v: Nervno-Myšečnye Bolezni, 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://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7e7c8ca36bdc603f1e9feabacf68c02
https://nmb.abvpress.ru/jour/article/view/385
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