Zobrazeno 1 - 10
of 81
pro vyhledávání: '"O I, Simonova"'
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
Autor:
N. V. Petrova, N. Y. Kashirskaya, D. K. Saydaeva, A. V. Polyakov, T.A. Adyan, O. I. Simonova, Y. V. Gorinova, E. I. Kondratyeva, V. D. Sherman, O. G. Novoselova, T. A. Vasilyeva, A. V. Marakhonov, M. Macek, E. K. Ginter, R. A. Zinchenko
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Cystic fibrosis (CF; OMIM #219700) is a common autosomal recessive disease caused by pathogenic variants (henceforward mutations) in the cystic fibrosis transmembrane conductance regulator gene (CFTR). The spectrum and frequencies
Externí odkaz:
https://doaj.org/article/592070c75b8342d5ae78cf9010e42d83
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b541ae3d95b754e4cc5b668982a72017
https://doi.org/10.21518/ms2022-011
https://doi.org/10.21518/ms2022-011
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::805fbba104bd36c2a74a2e60198f7e80
https://doi.org/10.21518/2079-701x-2022-16-18-56-63
https://doi.org/10.21518/2079-701x-2022-16-18-56-63
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17600386446e5c6aff198511aadc90fe
https://doi.org/10.31146/1682-8658-ecg-199-3-93-106
https://doi.org/10.31146/1682-8658-ecg-199-3-93-106
Autor:
A. A. Baranov, L. S. Namazova-Baranova, E. A. Vishneva, L. R. Selimzyanova, O. I. Simonova, E. V. Sereda, N. N. Rozinova, E. N. Tzygina, L. K. Katosova, A. V. Lazareva, Yu. V. Gorinova, O. V. Kustova
Publikováno v:
Педиатрическая фармакология, Vol 14, Iss 1, Pp 43-48 (2017)
The article presents the most modern positions of healthcare delivery for children with primary ciliary dyskinesia. Symptoms of this pathology in clinical practice vary that is conditioned by genetic heterogeneity of the disease. The most common dise
Externí odkaz:
https://doaj.org/article/184c21ffc1664041888105ad5625f93c
Autor:
A. A. Baranov, L. S. Namazova-Baranova, O. I. Simonova, E. A. Vishneva, L. R. Selimzyanova, E. V. Sereda, N. N. Rozinova, E. N. Tzygina, L. K. Katosova, A. V. Lazareva, Yu. V. Gorinova, O. V. Kustova
Publikováno v:
Педиатрическая фармакология, Vol 14, Iss 1, Pp 33-42 (2017)
The article is devoted to bronchiectases issue in children and reflects the most actual approaches to the diagnosis and management of patients with this pathology. Information on the true prevalence of bronchiectases both abroad and in Russia varies.
Externí odkaz:
https://doaj.org/article/a33ea86b912f4c1894e00c02631cc3e3
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f905e89a3eddadb4b19ffe6ac3af0bd8
https://doi.org/10.18093/0869-0189-2022-32-4-517-538
https://doi.org/10.18093/0869-0189-2022-32-4-517-538
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