Zobrazeno 1 - 4
of 4
pro vyhledávání: '"О. I. Simonova"'
Publikováno v:
Вопросы современной педиатрии, Vol 13, Iss 6, Pp 67-71 (2014)
Background: A long-term plating of Pseudomonas aeruginosa in patients with cystic fibrosis is a sign of damage of the lung tissues with rapid progression of the disease and decrease in a respiratory function. The early pathogen detection is necessary
Externí odkaz:
https://doaj.org/article/1d8d03860d774f98a1980cc7eb8579f2
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
Publikováno v:
Voprosy Sovremennoj Pediatrii, Vol 13, Iss 6, Pp 67-71 (2014)
Background: A long-term plating of Pseudomonas aeruginosa in patients with cystic fibrosis is a sign of damage of the lung tissues with rapid progression of the disease and decrease in a respiratory function. The early pathogen detection is necessary
Autor:
L. А. Shabalova, N.Yu. Kashirskaya, S. Yu. Semykin, L. S. Namazova-Baranova, А. V. Orlov, V.D. Sherman, М. Yu. Chernukha, Т. Ye. Gembitskaya, I. Asherova, S.S. Postnikov, Ye. K. Ginter, N. А. Il’yenkova, Т. А. Protasova, Ye. L. Amelina, I. P. Karimova, М. N. Kostyleva, I. D. Uspenskaya, D. Sergienko, А. F. Neretina, Ye. I. Kondrat’yeva, I. А. Shaginyan, I. K. Volkov, N. Kapranov, L. P. Nazarenko, О. I. Simonova, N. B. Merzlova, V.S. Nikonova, S. Krasovsky
Publikováno v:
Voprosy Sovremennoj Pediatrii, 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