Zobrazeno 1 - 10
of 35
pro vyhledávání: '"S. A. KRASOVSKY"'
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
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. Repina, S. A. Krasovsky, R. V. Rozhivanov, T. M. Sorokina, L. V. Shileiko, M. I. Shtaut, L. F. Kurilo, G. V. Shmarina, T. A. Adyan, N. Y. Kashirskaya, A. V. Polyakov, V. B. Chernykh
Publikováno v:
Андрология и генитальная хирургия, Vol 19, Iss 2, Pp 31-39 (2018)
Introduction. Cystic fibrosis (CF) is common monogenic disease resulted from CFTR gene mutations. A most of CF male patients are infertile due to the obstructive azoospermia, however, the mechanisms of the reduced fertility in male patients without t
Externí odkaz:
https://doaj.org/article/8b0ec55e0eca4a99b1a6b27e482bd461
Autor:
M. I. Shtaut, L. V. Schileiko, S. A. Repina, S. A. Krasovsky, G. V. Shmarina, T. M. Sorokina, L. F. Kurilo, V. B. Chernykh
Publikováno v:
Андрология и генитальная хирургия, Vol 18, Iss 4, Pp 69-76 (2018)
Introduction. Cystic fibrosis (CF) is a common genetic disorder associated with male infertility. Almost all men with CF are infertile due to obstructive azoospermia.The objective is to evaluate semen parameters, excretion of seminal fluid, and sperm
Externí odkaz:
https://doaj.org/article/5cc6c5560f7d41d7adb72df3e08b64ae
CHARACTERISTICS OF CYSTIC FIBROSIS IN THE KRASNODAR REGION ACCORDING TO A EUROPEAN REGISTER FOR 2011
Autor:
M. M. Khachiyan, E. I. Kondratieva, S. A. Krasovsky, A. V. Chernyak, E. I. Kleshenko, V. Y. Brisin
Publikováno v:
Кубанский научный медицинский вестник, Vol 0, Iss 7, Pp 77-83 (2017)
Creation of the Russian register of patients with cystic fibrosis and participation in the program European register is essential for patients in the region and in the country. Result of creating and analyzing annual data register should be the under
Externí odkaz:
https://doaj.org/article/a9e9abe2f01b434f89e38066402d0eea
Autor:
E. I. Kondratyeva, V. D. Sherman, E. L. Amelina, A. Yu. Voronkova, S. A. Krasovsky, N. Yu. Kashirskaya, N. V. Petrova, A. V. Chernyak, N. I. Kapranov, V. S. Nikonova, L. A. Shabalova
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 61, Iss 6, Pp 77-81 (2017)
The aim of this study was to investigate the prevalence of meconium ileus in a Russian population of patients with cystic fibrosis, its clinical and genetic characteristics and outcomes, by analyzing the data available in the 2014 registry of the Rus
Externí odkaz:
https://doaj.org/article/ac588fbd9e0c44a4a296fb9ed7cc446a
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:
S. V. Gautier, S. V. Golovinsky, V. N. Poptsov, O. M. Tsiroulnikova, S. A. Krasovsky, A. A. Mitrokhin, M. M. Vodneva, P. V. Sarygin, D. G. Akhaladze, E. А. Spirina
Publikováno v:
Vestnik Transplantologii i Iskusstvennyh Organov, Vol 18, Iss 2, Pp 110-116 (2016)
Cystic fibrosis (CF) is the third most common indication for lung transplantation. The recipients with CF have shown the best early and late survival rates after surgery. The special group of CF patients consists of those, whose airways were infected
Externí odkaz:
https://doaj.org/article/ed9fa74e6aef4c5d8ed2b9ef4a04f495
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