Zobrazeno 1 - 10
of 59
pro vyhledávání: '"S A Krasovsky"'
Autor:
V. V. Shmarin, D. A. Pukhalskaya, S. A. Krasovsky, Yu. M. Chudakova, A. V. Martynov, G. V. Shmarina
Publikováno v:
Медицинская иммунология, Vol 26, Iss 5, Pp 1045-1052 (2024)
Cystic fibrosis (CF) is one of the most common autosomal-recessive inherited diseases. The primary genetic defect in CF is aligned CFTR gene mutation which encodes a membrane protein functioning as cAMP-depended chloride channel. Classic phenotypical
Externí odkaz:
https://doaj.org/article/d2bd8462184245d5921303507e9f8409
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:
E. I. Kondratyeva, A. Yu. Voronkova, N. Yu. Kashirskaya, S. A. Krasovsky, M. A. Starinova, E. L. Amelina, S. N. Avdeev, S. I. Kutsev
Publikováno v:
PULMONOLOGIYA. 33:171-181
A registry of patients with cystic fibrosis (CF) of the Russian Federation has been compiled annually since 2011. Analysis of the national registry with large amounts of clinical and laboratory data helps understand changes in demographic indicators,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5782626d9492675e536014f2d3bd8cb6
https://doi.org/10.18093/0869-0189-2023-33-2-171-181
https://doi.org/10.18093/0869-0189-2023-33-2-171-181
Autor:
L V Vinokurova, G E Baimakanova, S A Krasovsky, S Yu Silvestrova, E A Dubtsova, G G Varvanina, D S Bordin
Publikováno v:
Терапевтический архив, Vol 90, Iss 10, Pp 84-88 (2018)
In order to optimize the therapy, the functional state of the pancreas (P) and the peculiarities of metabolic activity of intestinal microbiota in adults with cystic fibrosis (CF) were assessed. Materials and methods. 14 CF patients (20-34 years, 7 m
Externí odkaz:
https://doaj.org/article/e387a1ee1ace4d39a342b13818f035b0
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
Autor:
N A Krylova, E L Amelina, S A Krasovsky, N A Karchevskaya, E A Tarabrin, A M Gasanov, D F Ibragimova, S V Golovinsky
Publikováno v:
Терапевтический архив, Vol 89, Iss 12, Pp 51-55 (2017)
Aim. To evaluate the efficiency of nocturnal hyperalimentation in adult patients with cystic fibrosis (CF) and respiratory failure. Subjects and methods. The investigation enrolled 17 patients older than 18 years (mean age, 25.6±4.2 years) diagnosed
Externí odkaz:
https://doaj.org/article/3fda5702636446049a7e5e604a064977
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