Zobrazeno 1 - 5
of 5
pro vyhledávání: '"I.M. Galdina"'
Autor:
M.A. Gonchar, G.R. Muratov, O.L. Logvinova, E.M. Pushkar, E.P. Pomazunovskaya, E.V. Omelchenko, N.V. Shulga, I.M. Galdina, A.S. Zubko, N.V. Strebul
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 2, Pp 194-203 (2018)
The article deals with the modern principles for the diagnosis and treatment of peroxisomal biogenesis disorders of Zellweger syndrome spectrum according to the recommendations of the Global Foundation for Peroxisomal Disorders 2016. The authors pres
Externí odkaz:
https://doaj.org/article/84bb6d9348ae4a098b07ab8c27f7d706
Autor:
M.A. Gonchar, A.S. Senatorova, G.R. Muratov, E.V. Omelchenko, I.M. Galdina, E.M. Pushkar, N.N. Yablonskaya, T.F. Kolibaeva, A.A. Khomovskaya
Publikováno v:
Zdorovʹe Rebenka, Vol 12, Iss 4, Pp 527-530 (2017)
In the article, the authors analyze the literature, as well as the results of their own long-term experience in the diagnosis of genetically determined renal diseases accompanied by the development of chronic renal failure. The main causes of disease
Externí odkaz:
https://doaj.org/article/02d0d9bef1be4c11ad04b90b85879bd6
Autor:
N.N. Yablonskaya, E.V. Omelchenko, G.R. Muratov, I.M. Galdina, A.S. Senatorova, T.F. Kolibaeva, A.A. Khomovskaya, M.A. Gonchar, E.M. Pushkar
Publikováno v:
CHILD`S HEALTH. 12:527-530
In the article, the authors analyze the literature, as well as the results of their own long-term experience in the diagnosis of genetically determined renal diseases accompanied by the development of chronic renal failure. The main causes of disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3bcbf0b74c7aa7857a85d44608954ec
https://doi.org/10.22141/2224-0551.12.4.2017.107636
https://doi.org/10.22141/2224-0551.12.4.2017.107636
Autor:
A.S. Zubko, E.V. Omelchenko, M.A. Gonchar, E.M. Pushkar, G.R. Muratov, E.P. Pomazunovskaya, I.M. Galdina, N.V. Strebul, N.V. Shulga, O.L. Logvinova
Publikováno v:
CHILD`S HEALTH. 13:194-203
The article deals with the modern principles for the diagnosis and treatment of peroxisomal biogenesis disorders of Zellweger syndrome spectrum according to the recommendations of the Global Foundation for Peroxisomal Disorders 2016. The authors pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27f18fa35393bc099fb624f6076cb3f5
https://doi.org/10.22141/2224-0551.13.2.2018.129554
https://doi.org/10.22141/2224-0551.13.2.2018.129554
Autor:
M.A. Gonchar, E.M. Pushkar, G.R. Muratov, A.A. Homovskaya, T.F. Kolibaeva, A.S. Senatorova, N.N. Yablonskaya, I.M. Galdina
Publikováno v:
Sovremennaâ Pediatriâ, Iss 5(77), Pp 107-111 (2016)
The variety of the causes and symptoms of chronic renal failure, severe consequences of the disease attracted the attention of professionals of different specialties, thus, renal failure has long ceased to be a narrow problem which is solved only by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9728b0b7fab4d4d4acbb0857d5d5359a
https://med-expert.com.ua/en/clinical-observation-and-management-of-chronic-renal-failure-in-a-child-with-hereditary-determined-pathology-of-kidneys/
https://med-expert.com.ua/en/clinical-observation-and-management-of-chronic-renal-failure-in-a-child-with-hereditary-determined-pathology-of-kidneys/