Zobrazeno 1 - 10
of 48
pro vyhledávání: '"E. L. AMELINA"'
Autor:
E. I. Kondratyeva, A. I. Tlif, A. Yu. Voronkova, E. L. Amelina, N. Yu. Kashirskaya, S. A. Krasovsky, M. A. Starinova, T. L. Kuraeva
Publikováno v:
Сахарный диабет, Vol 26, Iss 5, Pp 418-426 (2023)
BACKGROUND: In recent decades, the life expectancy of patients with CF has increased, which leads to an increase in the frequency of conditions associated with impaired carbohydrate metabolism.AIM: to analyze the impact of cystic fibrosis-associated
Externí odkaz:
https://doaj.org/article/12a6b36fd78d452fba1270a44826dc92
Autor:
E. I. Kondratieva, S. V. Trishina, A. V. Yurieva, N. V. Komlev, V. A. Tanaga, V. A. Terentiev, A. Yu. Voronkova, E. L. Amelina, A. V. Chernyak, S. A. Krasovskiy, V. Yu. Brisin, M. M. Khachiyan, E. V. Vodovozova, E. A. Enina, L. N. Ledeneva, E. T. Yagubyants, M. M. Chepurnaya
Publikováno v:
Медицинский совет, Vol 0, Iss 4, Pp 108-119 (2022)
Introduction. Cystic fibrosis (CF) is a hereditary disease with genetic heterogeneity and clinical polymorphism. Expanding the range of knowledge about the characteristics of the course of the disease in different regions is important to achieve the
Externí odkaz:
https://doaj.org/article/bb59d1bd922144f289478f54bb633000
Publikováno v:
Медицинский совет, Vol 0, Iss 8, Pp 48-53 (2019)
Among diseases of ENT organs at patients with the CF prevails chronic rhinosinusitis. Stagnation of the infected dense slime in the paranasal sinus and violation of nasal breath aggravates weight of a course of lung pathology. Timely inspection and t
Externí odkaz:
https://doaj.org/article/2c2868767e6640fdb06999b99bf5bb01
Autor:
S. A. Krasovsky, E. L. Amelina, A. V. Chernyak, E. I. Kondratieva, J. V. Gorinova, O. G. Zonenko, D. F. Sergienko, A. R. Tatarsky
Publikováno v:
Медицинский совет, Vol 0, Iss 21, Pp 72-77 (2019)
A non-interventional prospective cohort study was conducted on adult patients with cystic fibrosis, who received mucolytic therapy with 7% NaCl solution combined with 0.1% hyaluronic acid (medical product Hyaneb) and 7% NaCl solution for 4 and 8 week
Externí odkaz:
https://doaj.org/article/b1391bb682a840169a28d588d7ea2e3b
Autor:
S. A. Krasovskiy, E. L. Amelina, U. V. Gorinova, A. V. Chernyak, M. V. Afanasjeva, N. A. Krilova, G. L. Shumkova, O. G. Zonenko, A. R. Tatarskiy
Publikováno v:
Клиническая практика, Vol 9, Iss 4, Pp 25-32 (2018)
Background: Evaluation of the main clinical and functional indicators and their relationship with the treatment and diagnostic care at different time periods can contribute to the development of further effective medical strategies and globally lead
Externí odkaz:
https://doaj.org/article/7c5d6f8496d34e43b1c92b494f6e0c73
Autor:
I. A. Shaginyan, M. Yu. Chernukha, L. R. Avetisyan, E. A. Siyanova, D. G. Kulyastova, O. S. Medvedeva, T. B. Priputnevich, D. Yu. Trofimov, A. V. Gordeev, E. I. Kondratieva, E. L. Amelina, S. A. Krasovskiy
Publikováno v:
Эпидемиология и вакцинопрофилактика, Vol 16, Iss 6, Pp 5-13 (2017)
Relevance. Life expectancy of cystic fibrosis patients mostly depends on the degree of respiratory system damage caused by opportunistic microorganisms, which is due to the fact that 90-95% of deaths of cystic fibrosis patients are caused by lung inf
Externí odkaz:
https://doaj.org/article/23b2824b74614215b0d1ef49fb034791
Autor:
S. V. POLIKARPOVA, E. I. KONDRATYEVA, L. A. SHABALOVA, N. V. PIVKINA, S. V. ZHILINA, A. Y. VORONKOVA, V. D. SHERMAN, V. S. NIKONOVA, N. I. KAPRANOV, N. Y. KASHIRSKAYA, S. Y. SEMYKIN, E. L. AMELINA, S. A. KRASOVSKY
Publikováno v:
Медицинский совет, Vol 0, Iss 15, Pp 84-89 (2016)
Chronic lower respiratory tract infection in patients with cystic fibrosis (CF) is the major factor determining the severity of the clinical course and prognosis of the disease. The purpose of the study was to investigate the prevailing respiratory m
Externí odkaz:
https://doaj.org/article/9fde4088c52346b292623b7a73c2d83c
Autor:
N. Yu. Kashirskaya, S. A. Krasovsky, A. V. Chernyak, V. D. Sherman, A. Yu. Voronkova, L. A. Shabalova, V. S. Nikonova, Yu. V. Gorinova, O. I. Simonova, E. L. Amelina, E. I. Kondrat’eva, N. I. Kapranov, N. V. Petrova, R. A. Zinchenko
Publikováno v:
Вопросы современной педиатрии, Vol 14, Iss 4, Pp 503-508 (2015)
Cystic fibrosis is multiple organ pathology that requires a complex treatment. Its standardization and pharmacoeconomic analysis are absolutely necessary. We performed a retrospective analysis of the trends in life expectancy of cystic fibrosis patie
Externí odkaz:
https://doaj.org/article/469ac005c5ab44a3b76219cbd0d47e2f
Autor:
S. A. Krasovskii, N. Yu. Kashirskaya, M. V. Usacheva, E. L. Amelina, A. V. Chernyak, Zh.K. Naumenko
Publikováno v:
Вопросы современной педиатрии, Vol 13, Iss 2, Pp 36-43 (2014)
Background: To establish features of a clinical course of a disease at patients depending on age of firstly determine diagnosis of cystic fibrosis. Patients and methods: We examined 130 patients with cystic fibrosis aged under 25 years old. Depending
Externí odkaz:
https://doaj.org/article/b34b275b0d2c4dc6aed3a9e34d11d79f
Autor:
S. A. Krasovskii, V. S. Nikonova, N. Yu. Kashirskaya, E. I. Kondrat'eva, A. V. Chernyak, N. I. Kapranov, E. L. Amelina, V. D. Sherman, V. A. Samoilenko, A. Yu. Voronkova, L. A. Shabalova, O. I. Simonova, M. V. Usacheva, V. V. Chernikov
Publikováno v:
Вопросы современной педиатрии, Vol 12, Iss 1, Pp 17-23 (2013)
The aim of this study was to assess different clinical and genetic, microbiological and functional features of patients with cystic fibrosis living in Moscow and Moscow region on the 31st December, 2010. The mean age of the patients was 12,1±9,6 yea
Externí odkaz:
https://doaj.org/article/f51de47f38dc47499787b8f479273248