Zobrazeno 1 - 10 of 34 pro vyhledávání: '"G R, Mutovin"'
1
Aicardi–Goutieres syndrome in children with idiopathic epilepsy
Autor: N. O. Bryukhanova, S. S. Zhilina, S. O. Aivazyan, T. V. Ananieva, M. S. Belenikin, T. V. Kozhanova, T. I. Meshcheryakova, R. A. Zinchenko, G. R. Mutovin, N. N. Zavadenko
Publikováno v: Rossijskij Vestnik Perinatologii i Pediatrii, Vol 61, Iss 2, Pp 68-75 (2016)
This article describes 9 clinical cases of Aicardi–Goutieres syndrome (AGS) in children admitted to the hospital of the Scientific and Practical Center of Medical Care for Children with Resistant Multifocal Epilepsy. Epilepsy, psychomotor retardati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4648179edcaafd9a95031fcbea3f04f
https://www.ped-perinatology.ru/jour/article/view/304
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2
An allelic variant of congenital Salih myopathy
Autor: M. S. Belenikin, S. S. Zhilina, A. A. Barinov, M. Yu. Shоrina, N. O. Bryukhanova, R. M. Magomedova, T. I. Meshcheryakova, A. N. Petrin, I. A. Demidova, G. G. Prokopiev, G. R. Mutovin, A. G. Prityko
Publikováno v: Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 3, Pp 89-93 (2016)
The paper describes the steps and problems of diagnosing congenital myopathy with early respiratory disorders. While differentially diagnosing, the authors consider congenital myopathies, in which early cardiac involvement is encountered. Since the c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::65c35516ebd68a499713276027ec7bbf
https://www.ped-perinatology.ru/jour/article/view/213
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5
[The frequency of chromosome aberrations in the lymphocytes of children with thyroid diseases living in Bryansk Province]
Autor: E K, Khandogina, S V, Zvereva, V A, Ageĭkin, L F, Marchenko, V V, Shakhtarin, G R, Mutovin, A P, Akif'ev
Publikováno v: Radiatsionnaia biologiia, radioecologiia. 35(5)
The number of unstable chromosome aberrations was determined in peripheral blood lymphocytes from 15 children with thyreopathology living in Klintsy (Bryansk Province); the mean age was 14 years. The number of dicentric chromosome is determined to be
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::13d58553b2a98dd4059605191687f034
https://pubmed.ncbi.nlm.nih.gov/7489093
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6
[The cytogenetic examination of different groups of children living in regions of Bryansk Province contaminated as a result of the Chernobyl accident]
Autor: E K, Khandogina, V A, Ageĭkin, S V, Zvereva, L F, Marchenko, G R, Mutovin, G P, Snigireva, R V, Lenskaia, V M, Buiankin, V V, Shakhtarin, A P, Akif'ev
Publikováno v: Radiatsionnaia biologiia, radioecologiia. 35(5)
The frequency of chromosome aberrations (CA) was studied in peripheral blood lymphocytes from healthy children and children with thyreopathology living in the city of Klintsy, Bryansk Province (contamination level up to 5 Ci/km2), and two Moscow grou
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4368d6fc1f5df0557d8bf8d1abf0ab0d
https://pubmed.ncbi.nlm.nih.gov/7489092
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7
[An evaluation of the radioprotective action of antioxidants on normal human cells and in genomic diseases by using different cytogenetic tests]
Autor: S V, Zvereva, G R, Mutovin, E K, Khandogina, L F, Marchenko, E V, Neudakhin, R G, Artamonov, A P, Akif'ev
Publikováno v: Radiobiologiia. 33(3)
In studying the radioprotective action of natural and synthesised antioxydants a decreased yield of chromosome aberrations with respect to those in untreated cells was noted in normal cells irradiated in phase G1 whereas no radioprotective effect was
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8748d74859fb03a4257e3917d1bb9446
https://pubmed.ncbi.nlm.nih.gov/8332722
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8
[State of the neuroendocrine system in children with congenital defects of development dependent on changes in the karyotype]
Autor: G R, Mutovin, Iu A, Kniazev, L F, Marchenko
Publikováno v: Pediatriia. (6)
Forty children with multiple congenital developmental abnormalities (MCDA) without any visible changes in the karyotype and 36 MCDA children having visible changes in the karyotype were examined for the status of the neuroendocrine system. The childr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e3dc8a0e9847ab47a61bd23a406fc625
https://pubmed.ncbi.nlm.nih.gov/2144336
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