Zobrazeno 1 - 10
of 10
pro vyhledávání: '"E. K. Zhekaite"'
Autor:
L. Ya. Klimov, S. V. Dolbnya, E. I. Kondratyeva, A. A. Dyatlova, E. A. Enina, V. A. Kuryaninova, A. N. Kasyanova, E. K. Zhekaite, D. V. Bobryshev, I. V. Markarova, T. M. Vdovina, A. A. Shaforost
Publikováno v:
Медицинский совет, Vol 0, Iss 2, Pp 240-249 (2019)
The article presents the results of vitamin D tests in children with cystic fibrosis and in healthy children living in the South of Russia. The study showed the high prevalence of vitamin D deficiency and inadequate levels in patients with cystic fib
Externí odkaz:
https://doaj.org/article/576a773de7d342e6b174a4e23231422d
Autor:
V. D. Sherman, E. I. Kondratieva, A. Y. Voronkova, N. Y. Kashirskaya, L. A. Shabalova, V. S. Nikonova, E. K. Zhekaite, S. I. Kutsev
Publikováno v:
Медицинский совет, Vol 0, Iss 18, Pp 124-128 (2017)
Study objective: comparative evaluation of clinical status of patients with cystic fibrosis (CF) 6–9 years, the diagnosis of which was established before the start of neonatal screening (NS) for MV in the Moscow region and in same age group since t
Externí odkaz:
https://doaj.org/article/946811a28f8543908e247106ef41bf70
Autor:
V. A. Strelnikova, A. G. Tsverava, D. Yu. Ovsyannikov, E. K. Zhekaite, O. B. Kondakova, P. V. Berejansky, K. V. Savostyanov, V. V. Gorev, M. I. Airapetyan, O. G. Topilin
Publikováno v:
PULMONOLOGIYA. 33:259-265
Primary ciliary dyskinesia (PCD) is an orphan disease associated with mutations in several genes. It is a ciliopathy, an abnormality of the cilia and flagella. Ciliopathies include the extremely rare Simpson - Golabi - Bemel syndrome (SSGB) type II.T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc44c962c4dad5cfcc59f6b4ed233c0a
https://doi.org/10.18093/0869-0189-2023-33-2-259-265
https://doi.org/10.18093/0869-0189-2023-33-2-259-265
Autor:
E. D. Nikolaeva, D. Yu. Ovsyannikov, V. A. Strel’nikova, D. P. Polyakov, T. V. Tronza, O. A. Karpova, I. R. Fatkhullina, Е. E. Bragina, O. A. Shchagina, M. A. Starinova, S. А. Krasovskiy, T. A. Kyian, E. K. Zhekaite
Publikováno v:
PULMONOLOGIYA. 33:198-209
Primary ciliary dyskinesia (PCD) (Online Mendelian Inheritance in Man - OMIM - #242650) is a rare hereditary disease, which is based on a defect in the ultrastructure of the cilia epithelium of the respiratory tract which leads to the motor function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94ff5f9eac7033db1a4568f7610405d3
https://doi.org/10.18093/0869-0189-2023-33-2-198-209
https://doi.org/10.18093/0869-0189-2023-33-2-198-209
Autor:
E. I. Kondratyeva, N. D. Odinaeva, E. K. Zhekaite, E. V. Pasnova, I. R. Fatkhullina, T. Yu. Maksimycheva, V. D. Sherman, S. I. Kutsev
Publikováno v:
PULMONOLOGIYA. 33:189-197
Pathogenetic therapy for the treatment of cystic fibrosis (CF) has been developed that modulates the CFTR protein and restores its activity as a chloride channel. This treatment is represented by CFTR modulators for various genotypes covering 85 - 90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2140ccfe91d3d04584580c439990461
https://doi.org/10.18093/0869-0189-2023-33-2-189-197
https://doi.org/10.18093/0869-0189-2023-33-2-189-197
Autor:
E. K. Zhekaite, E. I. Kondratyeva
Publikováno v:
PULMONOLOGIYA. 32:270-280
Pseudomonas aeruginosa is the most common highly pathogenic flora in patients with cystic fibrosis. It is associated with severe lung damage and affects life expectancy. According to the register of patients with cystic fibrosis in the Russian Federa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aef8c402a33161e85b32cf42d1d530bd
https://doi.org/10.18093/0869-0189-2022-32-2-270-280
https://doi.org/10.18093/0869-0189-2022-32-2-270-280
Autor:
E. I. Kondratyeva, E. V. Loshkova, I. N. Zakharova, Yu. F. Shubina, E. K. Zhekaite, V. S. Nikonova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 66, Iss 2, Pp 78-84 (2021)
The article presents the results of assessing the content of vitamin D in children and adolescents under 18 years old ( n =1501) in Moscow and the Moscow region, the average age was 13.45±11.76 years ( Me 15.00 years). The optimal level of 25(OH)D 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17351c0175dac54bf1337b91a75efcf8
https://doi.org/10.21508/1027-4065-2021-66-2-78-84
https://doi.org/10.21508/1027-4065-2021-66-2-78-84
Autor:
Kondratyeva, Elena Ivanovna, Sherman, V. D., M. A. Mukhina, O. I. Simonova, Kashirskaya, N. Yu, Malakhov, A. B., E. K. Zhekaite, Yu. V. Gorinova, E. V. Boitsova
Publikováno v:
Pediatria. Journal named after G.N. Speransky. 99:91-97
Objective of the research: to assess the prevalence and course of COVID-19 in children and adolescents with cystic fibrosis (CF) in the Russian Federation Materials and methods: up to September 1, 2020, 10 cases of COVID-19 in CF patients were regist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0053a57aff3f75718de119e7b2252fae
https://doi.org/10.24110/0031-403x-2020-99-6-91-97
https://doi.org/10.24110/0031-403x-2020-99-6-91-97
Autor:
E. I. Kondratyeva, S. A. Krasovsky, N. Yu. Kashirskaya, E. L. Amelina, E. K. Zhekaite, V. D. Sherman, O. I. Simonova, Yu. V. Gorinova, E. V. Boitsova, M. A. Mukhina, I. N. Butyugina, M. A. Makarova, A. B. Malakhov
Publikováno v:
PULMONOLOGIYA. 30:544-552
Since the beginning of the COVID-19 epidemic, the European cystic fibrosis society (ECFS) has decided to launch a special ECFS-COVID-19 program to collect information on the of COVID-19 characteristics in the patients with cystic fibrosis (CF). The r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::348459bb3517f5126d7ac11a248904e2
https://doi.org/10.18093/0869-0189-2020-30-5-544-552
https://doi.org/10.18093/0869-0189-2020-30-5-544-552
Autor:
E I, Kondratyeva, E K, Zhekaite, N D, Odinaeva, A Yu, Voronkova, V D, Sherman, E V, Loshkova, Yu L, Mel'yanovskaya, A E, Zod'binova, Yu F, Shubina, R M, Budzinsky
Publikováno v:
Voprosy pitaniia. 89(2)
Vitamin D deficiency is widespread in patients with cystic fibrosis (CF). From 2016 to 2018, prophylactic doses of vitamin D were prescribed for the patients of the Russian cystic fibrosis Center in accordance with the National cystic fibrosis consen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::289b574f8c23c5448ce9514d73ab08bc
https://pubmed.ncbi.nlm.nih.gov/32459908
https://pubmed.ncbi.nlm.nih.gov/32459908