Zobrazeno 1 - 10
of 82
pro vyhledávání: '"E A, Vishneva"'
Autor:
Polina S. Arimova, Leyla S. Namazova-Baranova, J. G. Levina, V. G. Kalugina, E. A. Vishneva, E. Yu. Kharitonova
Publikováno v:
Педиатрическая фармакология, Vol 18, Iss 3, Pp 214-220 (2021)
Background. Anti-inflammatory therapy is used to achieve and maintain asthma control, as well as respiratory function indicators monitoring. Telemedicine technologies can be used for this purpose, and it became particularly essential during the COVID
Externí odkaz:
https://doaj.org/article/99d190e5392e4343af549f15ea984ca7
Autor:
L. G. Levina, L. S. Namazova-Baranova, E. A. Vishneva, K. S. Volkov, K. Y. Efendieva, A. A. Alekseeva, V. G. Kalugina, P. S. Arimova
Publikováno v:
Педиатрическая фармакология, Vol 18, Iss 2, Pp 118-133 (2021)
Background. The prevalence of various allergic diseases has increased worldwide in recent decades. Allergy diagnosis in children should be economically optimal and as sparing as possible, while ensuring the high quality of medical care. Objective. Th
Externí odkaz:
https://doaj.org/article/e3815b3466914c2f96c14b8dace073f7
Publikováno v:
Juvenis Scientia, Iss 7, Pp 4-7 (2018)
In the modern worldcardiovascular pathology associated with atherosclerosis has become one of the leading causes of morbidity and mortality of the population, besides, the combined lesion of several vascular pools leads to a worse prognosis at the mo
Externí odkaz:
https://doaj.org/article/2206b489057e44cb833d7ff12ebe554c
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. G. Bokuchava, L. S. Namazova-Baranova, A. A. Alekseeva, K. E. Efendieva, E. A. Vishneva, Yu. G. Levina, N. I. Voznesenskya, E. А. Dobrinina, V. G. Kalugina
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 6, Pp 544-548 (2017)
Background: Children with allergic diseases, especially bronchial asthma, are in need of protection from acute respiratory infections, as anti-epidemic measures cannot prevent the spread of influenza; vaccination remains the best means of prevention.
Externí odkaz:
https://doaj.org/article/62e2b9d70d4b4c01b8099992c1e654e4
Autor:
A. A. Baranov, L. S. Namazova-Baranova, К. V. Savostianov, Т. V. Margieva, E. A. Vishneva, G. Т. Yakhyaeva
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 6, Pp 539-543 (2017)
Hypophosphatasia is a rare genetic disorder caused by deficiency of tissue-specific alkaline phosphatase as a result of mutations in the ALPL gene. Depending on the form and severity of the disease, pathology may spawn in utero, in childhood or in ad
Externí odkaz:
https://doaj.org/article/de9728406f654a64afb9d5ef57fb35f8
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:
A. G. Chuchalin, S. N. Avdeev, Z. R. Aisanov, A. S. Belevskiy, O. S. Vasil’eva, N. A. Geppe, G. L. Ignatova, N. P. Knyazheskaya, A. B. Malakhov, N. I. Meshcheryakova, N. M. Nenasheva, R. S. Fassakhov, R. M. Khaitov, N. I. Il’ina, O. M. Kurbacheva, N. G. Astafieva, I. V. Demko, D. S. Fomina, L. S. Namazova-Baranova, A. A. Baranov, E. A. Vishneva, G. A. Novik
Publikováno v:
PULMONOLOGIYA. 32:393-447
Bronchial asthma is a heterogeneous disease that requires identification of its phenotype and a personalized approach to therapy. At the same time, despite a wide range of therapeutic options, many patients with asthma cannot achieve control over the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebeb06b8468245cfe8cea800e6ea8d2e
https://doi.org/10.18093/0869-0189-2022-32-3-393-447
https://doi.org/10.18093/0869-0189-2022-32-3-393-447
Publikováno v:
Педиатрическая фармакология, Vol 13, Iss 5, Pp 488-493 (2016)
Phytotherapy is one of the oldest treatment methods. Studies and conclusions of the World Health Organization (WHO) Expert evidence of the trend towards greater demand for alternative treatments, including herbal medicine. The article presents such a
Externí odkaz:
https://doaj.org/article/14af059173484271aa0d663e984ed749