Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M. I. Yablonskaya"'
Publikováno v:
RUDN Journal of Agronomy and Animal Industries, Vol 0, Iss 1, Pp 15-20 (2016)
In vitro coculture of plant tissue explants with beneficial microorganisms enhance their tolerance to abiotic and biotic stresses. The induced resistance response caused by the inoculants is referred to as “biotization”. There is enough experimen
Externí odkaz:
https://doaj.org/article/b3482fea947a488b97f2ec2b39291e1d
Autor:
M. I. Yablonskaya, E. A. Nikolayeva, A. N. Semyachkina, O. N. Komarova, M. L. Babayan, M. N. Kharabadze, Yu. I. Davydova, A. R. Zabrodina
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 63, Iss 2, Pp 64-69 (2018)
IXa glycogenosis is the most common of the currently known 15 types of glycogenosis. The disease has X-linked recessive inheritance, is caused by mutations in the PHKA2 gene localized on the short arm of X chromosome in the Хр22.13 region. The main
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9641c4ddf759534aa4e9df5d7cfdb928
https://www.ped-perinatology.ru/jour/article/view/647
https://www.ped-perinatology.ru/jour/article/view/647
Autor:
A. N. Semyachkina, V. S. Sukhorukov, T. M. Bukina, M. I. Yablonskaya, E. S. Merkuryeva, M. N. Kharabadze, E. A. Proskurina, E. Yu. Zakharova, A. V. Brydun, P. A. Shatalov, P. V. Novikov
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 59, Iss 4, Pp 48-55 (2016)
The paper gives the data available in the literature, which reflect the manifestations, diagnosis, and current treatments of the rare (orphan) inherited disease glycogen storage disease type II or Pomp disease in children, as well as its classificati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::95c54d67c4391bd6b235b6611a76f246
https://www.ped-perinatology.ru/jour/article/view/58
https://www.ped-perinatology.ru/jour/article/view/58
Autor:
E. A. Nikolaeva, M. I. Yablonskaya, M. N. Kharabadze, Yu. I. Davydova, O. N. Komarova, P. V. Novikov
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 2, Pp 66-71 (2016)
The term phenylketonuria encompasses some genetically heterogeneous diseases from a group of hereditary amino acid metabolic disorders, the key biochemical sign of which is a steady increase in blood phenylalanine levels – hyperphenylalaninemia. Ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::f9de301cb885a8627acbe45166d5ea81
https://www.ped-perinatology.ru/jour/article/view/99
https://www.ped-perinatology.ru/jour/article/view/99
Autor:
M. I. Yablonskaya, P. V. Novikov, E. G. Agapov, I. V. Zolkina, E. A. Yuryeva, M. N. Kharabadze
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 4, Pp 57-62 (2016)
The rare hereditary diseases encountered in the practice of pediatricians, pediatric neurologists, and geneticists include Lesch—Nyhan syndrome associated with purine metabolic disorders caused by mutations in the HPRT1 gene encoding the enzyme hyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::6b1609695d09db92a1e6fd9bffa0b58b
https://www.ped-perinatology.ru/jour/article/view/136
https://www.ped-perinatology.ru/jour/article/view/136
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 60, Iss 5, Pp 26-32 (2016)
The paper reviews the current literature on immune-mediated pediatric epilepsies. It describes the clinical picture, laboratory diagnosis, and treatment of autoimmune encephalitides (limbic encephalitis and anti-NMDA-receptor antibody encephalitis),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::72e9c5c554c4a0542b7b1f52e35cbf2c
https://www.ped-perinatology.ru/jour/article/view/151
https://www.ped-perinatology.ru/jour/article/view/151
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 61, Iss 3, Pp 51-57 (2016)
The common cause of mitochondrial diseases is mutations in the POLG1 gene encoding the catalytic subunit of DNA-polymerase gamma that is responsible for the replication and repair of mitochondrial DNA. Diseases associated with POLG1 gene defects are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a86603d266a42c6f8648eaef1d088b6
https://doi.org/10.21508/1027-4065-2016-61-3-51-57
https://doi.org/10.21508/1027-4065-2016-61-3-51-57