Zobrazeno 1 - 10
of 70
pro vyhledávání: '"O I Simonova"'
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:
Медицинский совет, Vol 0, Iss 4, Pp 120-127 (2022)
The article describes the features of mucolytic therapy in patients with cystic fibrosis, as the leading pathogenetic mechanism of the disease lies in the compromised mucociliary transport due to the presence of viscous secretions. Particular attenti
Externí odkaz:
https://doaj.org/article/ded6ceba80f54b00b5ba1331de93bbec
Autor:
N. V. Liabina, O. I. Simonova, I. V. Shirokova, E. L. Semikina, E. F. Mavrikidi, I. I. Kondrakhina, Yu. V. Gorinova, V. A. Kerimova
Publikováno v:
Медицинский совет, Vol 0, Iss 1, Pp 226-234 (2022)
Introduction. Cystic fibrosis associated (related) diabetes mellitus (CFDM) is one of the most common severe complications of cystic fibrosis. Today, the issue of the goodness of a single measurement of fasting blood glucose, glycated hemoglobin and
Externí odkaz:
https://doaj.org/article/b0e08dae52234f4f88a251fc6620faec
Publikováno v:
Meditsinskiy sovet = Medical Council. :172-181
Introduction. Progression of pulmonary and heart failure often causes death in patients with cystic fibrosis (95%). Therefore, monitoring of lung condition is very important for patients with cystic fibrosis (CF). Structural changes are visualized by
Publikováno v:
Meditsinskiy sovet = Medical Council. 16:56-63
The article describes the mechanisms of mucostasis and lung damage in cystic fibrosis. Types of mucolytic therapy and importance of inhalation therapy are considered. The authors presented their own classification of mucoactive agents. The principle
Autor:
N. V. Lyabina, O. I. Simonova, I. V. Shirokova, V. P. Chernevich, A. S. Batyrova, А. A. Marushina, A. I. Khavkin, A. Е. Krasnovidova, N. Yu. Kashirskaya
Publikováno v:
Experimental and Clinical Gastroenterology. :93-106
Th e article presents a review on a cystic fibrosis-r elated diabetes, a severe complication of cystic fi brosis in children, which has acquired increasing importance and revealed to contribute in prognosis of the disease in recent years. Which inc
Autor:
E. I. Kondratyeva, S. N. Avdeev, Yu. L. Mizernitskiy, A. V. Polyakov, M. Yu. Chernukha, O. V. Kondratenko, L. S. Namazova-Baranova, E. A. Vishneva, L. R. Selimzyanova, O. I. Simonova, T. E. Gembitskaya, E. E. Bragina, S. A. Rachina, A. B. Malakhov, D. P. Polyakov, N. D. Odinaeva, S. I. Kutsev
Publikováno v:
PULMONOLOGIYA. 32:517-538
Primary ciliary dyskinesia (PCD) is a rare hereditary disease from the group of ciliopathies, which is based on a defect in the cilia ultrastructure of the respiratory epithelium and similar structures (sperm flagella, villi of the fallopian tubes, v
Autor:
D. A. Blagovidov, M. P. Kostinov, O. I. Simonova, A. D. Shmit'ko, N. I. Burkina, M. K. Shahnazaryan
Publikováno v:
Эпидемиология и вакцинопрофилактика, Vol 15, Iss 2, Pp 55-66 (2016)
Chronic Pseudomonas aeruginosa infection is the most common cause of the failure in treatment and of adverse outcomes among children with congenital malformation of the lung (CML) and cystic fibrosis (CF). Purpose: To evaluatae the safety of anti Pse
Externí odkaz:
https://doaj.org/article/3fd7ba53ae854b15b251fcfaeae7ba6e
Autor:
O. I. Simonova
Publikováno v:
Вопросы современной педиатрии, Vol 14, Iss 4, Pp 509-513 (2015)
The article discusses the use of N-acetylcysteine in pediatric practice and examines various clinical effects of acetylcysteine, including in acute respiratory infections in children, and peculiarities of its application. The causes for the phenomeno
Externí odkaz:
https://doaj.org/article/041842b6b899450cb45101de22355e75
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