Zobrazeno 1 - 10
of 122
pro vyhledávání: '"M. . Voevoda"'
Autor:
V. . Gafarov, M. . Voevoda, E. . Gromova, V. . Maximov, A. . Gafarova, I. . Gagulin, N. . Yudin, T. . Mishakova, D. . Panov
Publikováno v:
Обозрение психиатрии и медицинской психологии имени В.М. Бехтерева, Vol 0, Iss 1, Pp 66-70 (2018)
Objective: to study the association polimorfizma-G308A gene tumor necrosis factor TNF-α and sleep disturbances in the male population aged 25-64 in metropolis of Western Siberia (Novosibirsk). Methods: Under the III screening of the WHO program «MO
Externí odkaz:
https://doaj.org/article/d6aaff0552494fd89b862352c53b1a89
Autor:
V. A. Ivanisenko, E. V. Gaisler, N. V. Basov, A. D. Rogachev, S. V. Cheresiz, T. V. Ivanisenko, P. S. Demenkov, E. L. Mishchenko, O. P. Khripko, Yu. I. Khripko, S. M. Voevoda, T. N. Karpenko, A. J. Velichko, M. I. Voevoda, N. A. Kolchanov, A. G. Pokrovsky
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-14 (2022)
Abstract Metabolomic analysis of blood plasma samples from COVID-19 patients is a promising approach allowing for the evaluation of disease progression. We performed the metabolomic analysis of plasma samples of 30 COVID-19 patients and the 19 contro
Externí odkaz:
https://doaj.org/article/caf7fbbe612f401eb60d121fe206d2bd
Autor:
O. D. Rymar, S. M. Voevoda, E. V. Shakhtshneider, E. M. Stakhneva, S. V. Mustafina, L. V. Shcherbakova
Publikováno v:
Ожирение и метаболизм, Vol 18, Iss 2, Pp 180-189 (2021)
Background: Hyperprolactinemia is one of the most common hypothalamic-pituitary-endocrine disorders in women of reproductive age, with the highest frequency at the age of 25–44 years. In addition to influencing the reproductive system, it is import
Externí odkaz:
https://doaj.org/article/e9aec3b0bbd34f8f9f0e12a182d87cad
Autor:
S. Boytsov, A. Katapano, O. Barbarash, M. Yezhov, A. Meshkov, M. Voevoda, V. Gurevich, V. Kashtalap, D. Duplyakov, N. Vezikova, D. Sadykova
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 20, Iss 1 (2021)
Externí odkaz:
https://doaj.org/article/7b03164bdbc046b2b33ec735f36c2d04
Autor:
S. V. Mustafina, V. I. Alferova, S. M. Voevoda, D. V. Denisova, L. V. Scherbakova, E. M. Stakhneva, O. D. Rymar
Publikováno v:
Clinical and experimental thyroidology. 18:13-22
AIM: To study anthropometric, biochemical and hormonal characteristics of women aged 25-44 with different levels of thyroid- stimulating hormone, prolactin and leptin.MATERIALS AND METHODS: From a representative sample of the young population of the
Autor:
V. I. Alferova, S. V. Mustafina, O. D. Rymar, S. M. Voevoda, L. V. Shcherbakova, E. M. Stakhneva, D. V. Denisova
Publikováno v:
Сибирский научный медицинский журнал. 43:111-123
Reports that the risk of developing cardiovascular diseases in obesity is not the same, led to the allocation of metabolically healthy and unhealthy phenotypes (MHP and MUHP), this concept is based on the ability of adipose tissue to produce a number
Autor:
S. M. Voevoda, L. V. Shcherbakova, D. V. Denisova, E. V. Shakhtshneyder, Yu. I. Ragino, E. M. Stakhneva, O. D. Rymar
Publikováno v:
Атеросклероз, Vol 14, Iss 4, Pp 67-72 (2018)
Objective: to study the association of prolactin with indicators of carbohydrate and lipid metabolism in women of reproductive age 25-45 years. Materials and methods: Clinical and laboratory examination of a random representative sample of women 25-4
Externí odkaz:
https://doaj.org/article/5599ff71b71a409aa34a1e611cc9e136
Publikováno v:
Сибирский научный медицинский журнал. 42:79-86
Aim. To study the spectrum of variants in the PRL, PRLR, PRLHR genes in women of reproductive age with non-tumor hyperprolactinemia. Material and methods. In women with non-tumor hyperprolactinemia (n = 15), targeted high-throughput sequencing of the
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Autor:
M I Voevoda, A A Ivanova, E V Shakhtshneider, A K Ovsyannikova, S V Mikhailova, K S Astrakova, S M Voevoda, O D Rymar
Publikováno v:
Терапевтический архив, Vol 88, Iss 4, Pp 117-124 (2016)
To verify the type of diabetes mellitus (DM) remains an extremely important problem in endocrinology, as along with types 1 and 2 DM there are rarer hereditary types of DM, including maturity-onset diabetes of the young (MODY). The latter is a geneti
Externí odkaz:
https://doaj.org/article/f4bb730962c046e6bb96d1f201a88a02