Zobrazeno 1 - 10
of 15
pro vyhledávání: '"S. Yu. Semykin"'
Role of Anaerobic Flora in Development of Bronchopulmonary Infection in Children with Mucoviscidosis
Publikováno v:
Антибиотики и Химиотерапия, Vol 54, Iss 3-4, Pp 26-28 (2020)
Externí odkaz:
https://doaj.org/article/7f5239bd2019425e8d36deba7297ce73
Autor:
Ye. L. Amelina, I. K. Asherova, I. K. Volkov, Т. Ye. Gembitskaya, Ye. K. Ginter, N. А. Il’yenkova, N. I. Kapranov, I. P. Karimova, N. Yu. Kashirskaya, Ye. I. Kondrat’yeva, М. N. Kostyleva, S. А. Krasovsky, N. B. Merzlova, L. P. Nazarenko, L. S. Namazova-Baranova, А. F. Neretina, V. S. Nikonova, А. V. Orlov, S. S. Postnikov, Т. А. Protasova, S. Yu. Semykin, D. F. Sergienko, О. I. Simonova, I. D. Uspenskaya, М. Yu. Chernukha, L. А. Shabalova, I. А. Shaginyan, V. D. Sherman
Publikováno v:
Вопросы современной педиатрии, Vol 13, Iss 6, Pp 89-95 (2014)
The pulmonary drug administration for the treatment of a pulmonary affection in cystic fibrosis is highly effective. This consensus document summarizes data on inhalation intake of bronchodilators, mucolytics, anti-inflammatory drugs, including gluco
Externí odkaz:
https://doaj.org/article/6524667aa0ed4fb08cf3767cd4dcf923
Autor:
O. I. Simonova, О. А. Ereshko, D. А. Makarova, S. Yu. Semykin, I. Yu. Asaturova, V. Yu. Brisin, K. S. Volkov, А. Yu. Tomilova
Publikováno v:
Вопросы современной педиатрии, Vol 13, Iss 4, Pp 110-117 (2014)
Background: The basis of the treatment of patients with cystic fibrosis (CF) is kinesitherapy — a special respiratory gymnastics and drainage of a bronchial tree. The increase of efficiency of a complex of medical rehabilitation measures can be rea
Externí odkaz:
https://doaj.org/article/d46d2526b13b4da78629e86bf1b66bf7
Autor:
Yu.A. Bocharova, S. Yu. Semykin, I V Chebotar, A V Lyamin, O.V. Kondratenko, N I Fedorova, S.V. Polikarpova, S.V. Zhilina, Dmitriy Korostin, A V Chaplin, N. A. Mayansky, Tatiana Savinova
Publikováno v:
Russian Clinical Laboratory Diagnostics. 66:629-634
Cystic fibrosis (CF) is a common genetic disease, manifested by airway obstruction and chronic respiratory infection. The most prevalent infectious agent in airways of CF patients is Pseudomonas aeruginosa. This study aimed to determine sequence-type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925274199f0c17f07569249138571dc5
https://doi.org/10.51620/0869-2084-2021-66-10-629-634
https://doi.org/10.51620/0869-2084-2021-66-10-629-634
Autor:
N.Yu. Kashirskaya, Elena Kondratyeva, A.Yu. Voronkova, M. Starinova, O. I. Simonova, V. V. Shadrina, D. Sergienko, S. Yu. Semykin
Publikováno v:
PULMONOLOGIYA. 31:159-166
Identifying the initial manifestations of pulmonary functional disorders associated with cystic fibrosis (CF) is essential for timely correction of the therapy and improvement of the prognosis.The aim of the study was to identify the age periods with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4402c9f072239ea13c19a4ced5c27d9
https://doi.org/10.18093/0869-0189-2021-31-2-159-166
https://doi.org/10.18093/0869-0189-2021-31-2-159-166
Autor:
Yu. A. Bocharova, T. A. Savinova, A. V. Lyamin, O. V. Kondratenko, S. V. Polikarpova, S. V. Zhilina, N. I. Fedorova, S. Yu. Semykin, A. V. Chaplin, D. O. Korostin, N. A. Mayansky, I. V. Chebotar
Publikováno v:
Klinicheskaia laboratornaia diagnostika. 67(5)
Stenotrophomonas maltophilia is a common opportunistic microorganism and an important respiratory pathogen in cystic fibrosis (CF). The aim of this study was to determine antimicrobial resistance phenotypes, sequence-types (ST) and genetic determinan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22c7ecccd9d3868d118ab6aa037b7c8e
https://pubmed.ncbi.nlm.nih.gov/35613352
https://pubmed.ncbi.nlm.nih.gov/35613352
Autor:
S A Krasovsky, E L Amelina, A V Chernyak, V S Nikonova, A Yu Voronkova, N Yu Kashirskaya, N I Kapranov, V P Chistyakova, V A Samoilenko, S Yu Semykin, O I Simonova, N V Petrova, Yu V Gorinova, A G Chuchalin
Publikováno v:
Терапевтический архив, Vol 84, Iss 3, Pp 54-58 (2012)
Aim. To estimate survival median and its changes, number of patients over 18 years of age for 1991—2000 and 2001-2010 for 20-year period (1991-2010), to elucidate factors affecting survival for 2001—2010 in mucoviscidosis children living in Mosco
Externí odkaz:
https://doaj.org/article/b6d3026bd05d474ab3ca03632235560b
Publikováno v:
Russian Pediatric Journal. 21:188-192
A rare clinical case of the development of acute pancreatitis in adolescents with a mixed form of cystic fibrosis having a “mild genotype” of the disease (“mild mutation” of the CFTR gene) and simultaneously the presence of cystic fibrosis-as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::181c75251901ae6bf7062b54e1803adc
https://doi.org/10.18821/1560-9561-2018-21-3-188-192
https://doi.org/10.18821/1560-9561-2018-21-3-188-192
CLINICAL AND GENETIC FEATURES OF CONNECTIVE TISSUE DYSPLASIA SYNDROME IN CYSTIC FIBROSIS IN CHILDREN
Publikováno v:
Russian Pediatric Journal. 21:203-207
The aim of the study was to determine the clinical and genetic features of the syndrome of undifferentiated connective tissue dysplasia (CTD) in cystic fibrosis (CF) children and the possible modifying effect of polymorphisms of connective tissue gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f9978c46100d5d9310e146ca9f170c7
https://doi.org/10.18821/1560-9561-2018-21-4-203-207
https://doi.org/10.18821/1560-9561-2018-21-4-203-207
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 63, Iss 5, Pp 20-28 (2018)
The article considers the issue of cystic fibrosis – a monogenic autosomal recessive disease. It describes the history of the CFTR gene discovery, the further search for modifier genes to explain the variability of the clinical manifestations of cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43d54c680b890c214793a3a66fc1abe
https://www.ped-perinatology.ru/jour/article/view/718
https://www.ped-perinatology.ru/jour/article/view/718