Zobrazeno 1 - 5
of 5
pro vyhledávání: '"T Yu, Belyaeva"'
Autor:
E. M. Tolstova, N. S. Zaytseva, O. V. Zaytseva, S. R. Kuzina, D. V. Khaspekov, E. V. Efimova, I. V. Turishchev, T. Yu. Belyaeva
Publikováno v:
Медицинский совет, Vol 0, Iss 1, Pp 236-242 (2022)
Concomitant congenital malformations are an actual problem in pediatrics. Association of tracheobronchial tree anomalies and congenital heart disease (CHD) could be the cause of the patient’s condition deterioration before and after cardiac surgery
Externí odkaz:
https://doaj.org/article/21d3b301db4c41bbb04e0ff50089e635
Takayasu’s arteritis in a child with prolonged fever. Differential diagnosis. Clinical case analysis
Autor:
N. A. Chegodaeva, E. B. Olkhova, O. V. Zaytseva, N. A. Savitskaya, E. E. Lokshina, I. I. Khmelkova, N. R. Shamratova, T. Yu. Belyaeva
Publikováno v:
Медицинский совет, Vol 0, Iss 11, Pp 140-147 (2021)
Takayasu’s arteritis is a chronic granulomatous arteritis with predominant involvement of the aorta and its main branches. It occurs both in youth and childhood, manifests between the ages of 10 and 30 years, female patients predominate. This artic
Externí odkaz:
https://doaj.org/article/0c827009faca4cf4b92b099a3cea808c
Publikováno v:
Meditsinskiy sovet = Medical Council. :28-33
The problem of community-acquired pneumonia in children remains relevant at the present time. Complicated forms, which include pleural empyema, abscess, necrotizing pneumonia, bronchopleural fistulas and acute respiratory distress syndrome do not dec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f312cdfca37b53d9a9e69985132770c
https://doi.org/10.21518/ms2023-025
https://doi.org/10.21518/ms2023-025
Autor:
T. Yu. Belyaeva, M. V. Besedina, I. V. Turishchev, O. V. Zaytseva, N. S. Zaytseva, Moscow State Medical, E. E. Lokshina, E. M. Tolstova
Publikováno v:
Practical Medicine. 18:6-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3819444f7fcf4261207360a53d1cf4ba
https://doi.org/10.32000/2072-1757-2020-3-6-13
https://doi.org/10.32000/2072-1757-2020-3-6-13
Autor:
N I, Melnikova, E V, Kartseva, A S, Kirsanov, I A, Strogonov, L N, Ageeva, G D, Kharitonova, E B, Olhova, T Yu, Belyaeva
Publikováno v:
Anesteziologiia i reanimatologiia. 60(3)
Diagnosis of amino acid metabolism disorders according to the clinics without laboratory diagnosis is almost impossible in infants with a history of neonatal and/or premorbid background and multi-organ failure. Mortality due to hereditary tyrosinemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a4244d871a064e3b4fc8ec2d4341fda1
https://pubmed.ncbi.nlm.nih.gov/26415289
https://pubmed.ncbi.nlm.nih.gov/26415289