Zobrazeno 1 - 10
of 69
pro vyhledávání: '"M.A. Gonchar"'
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 6, Pp 595-601 (2018)
The article shows a three-level approach to the diagnosis of glycine encephalopathy by the example of a clinical case. The article considers the modern etiology of the disease, based on molecular genetic testing of biallelic genes by DNA sequencing a
Externí odkaz:
https://doaj.org/article/0e0ccef3c44c4503aa8122b5e9cea27e
Autor:
M.A. Gonchar
Publikováno v:
Неонатологія, хірургія та перинатальна медицина, Vol 4, Iss 2(12) (2019)
Problems of diagnosis of neonatal arrhythmias, the main types of rhythm disorders in newborns, the modern approaches to the treatment of arrhythmias in the fetus and newborn are discussed in the article.
Externí odkaz:
https://doaj.org/article/72b595c5ba584cf5b7406e6bc1df0e39
Autor:
O.L. Logvinova, M.A. Gonchar
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 5, Pp 516-523 (2018)
The article presents a modern understanding of the components of the surfactant, the functions of non-serum proteins SP-A, SP-B, SP-C and SP-D. The history of the discovery of protein deficiencies SP-B, SP-C and ABCA3 is described. The authors had an
Externí odkaz:
https://doaj.org/article/f1b08c4dce2142f886fc84801db66d67
Autor:
O.L. Logvinova, M.A. Gonchar
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 5, Pp 502-505 (2018)
This article is a review of the modern world literature on the brain-lung-thyroid syndrome in children. The authors focused on the etiology and features of ontogenesis of the involved organs in the presence of NKX2-1 gene mutation. Particular attenti
Externí odkaz:
https://doaj.org/article/0af8d10aa455488a9333368542be5b15
Autor:
M.A. Gonchar, G.S. Senatorova, O.L. Logvinova, G.R. Muratov, E.M. Pushkar, E.N. Kryzhanovskaya, T.B. Ishchenko, O.P. Pomasunovska, O.V. Bondar, T.N. Ishchenko, V.V. Kornienko
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 3, Pp 294-301 (2018)
Mycoplasma pneumoniae takes the leading place in the etiology of community-acquired pneumonia in children. The article presents the course of macrolide-resistant mycoplasmal pneumonia and modern treatment strategy based on the clinical observation of
Externí odkaz:
https://doaj.org/article/3c4a5b3902d74a06a19bcc424084f4ca
Autor:
Yu.G. Antipkin, A.P. Volosovets, V.G. Maidannik, V.S. Berezenko, R.A. Moiseenko, O.V. Vygovskaya, S.P. Krivopustov, V.N. Zabolotko, N.L. Aryaev, A.E. Abaturov, T.A. Kryuchko, G.V. Beketova, O.M. Okhotnikova, S.A. Kramarev, V.I. Petrenko, A.F. Levitsky, Yu.V. Maroushko, Т.V. Maroushko, Yu.S. Piatnytskyi, O.G. Shadrin, E.N. Mukvich, I.V. Mikichak, T.P. Kosovskaya, V.P. Lisak, Yu.V. Sorokolat, A.V. Tereshchenko, N.V. Banadyga, L.V. Besh, Yu.K. Bolbot, L.N. Boyarskaya, A.B. Volosyanko, M.A. Gonchar, V.M. Dudnik, A.V. Zubarenko, T.M. Klimenko, E.K. Koloskova, G.A. Lezhenko, L.S. Ovcharenko, А.S. Senatorova, A.I. Smiyan, T.V. Sorokman, T.V. Stoeva, O.E. Chernishova, О.A. Tsodikova, T.V. Bondarenko, M.V. Golyak, O.R. Znak, N.N. Efremova, T.E. Karchevich, O.V. Lukyanenko, A.V. Luneva, N.M. Marchenko, S.L. Mikhno, S.G. Pisarenko, T.M. Pokotilova, E.I. Rubanova, O.V. Stashko, N.A. Shmalko, K.N. Shcherbinska, E.V. Mozyrskaya
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 2, Pp 142-152 (2018)
The article deals with the problems of increasing the incidence and prevalence of childhood diseases during 1994–2016 against the background of a global reduction in the staffing of children’s specialists by 1.7 times, with an extremely inadequat
Externí odkaz:
https://doaj.org/article/ccf917b01e5d49a8add94768582378b1
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
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 1, Pp 106-114 (2018)
The article presents own clinical observation of the chromosome 22q11.2 microdeletion syndrome in a child with congenital heart disease. Phenotype also includes facial skull anomalies, immune disorders, developmental delay and even cognitive deficits
Externí odkaz:
https://doaj.org/article/4fa5c0490d8c4ef5903bf17d41849413
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:
O.L. Logvinova, M.A. Gonchar
Publikováno v:
Zdorovʹe Rebenka, Vol 13, Iss 6, Pp 585-587 (2018)
The article presents a modern view on the problem of pulmonary interstitial glycogenosis, describes a typical clinical and morphological picture of the disease, and considers the disease etiology and the possibility of pulmonary interstitial glycogen
Externí odkaz:
https://doaj.org/article/f194b673a6d64eab9201380692128cd4