Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Iurii Sadovnychenko"'
Autor:
Olena Fedota, Iurii Sadovnychenko, Mykola Hryshchenko, Kostiantyn Tyshchenko, Yana Hryshchenko
Publikováno v:
Актуальні проблеми сучасної медицини, Vol 3, Pp 20-27 (2019)
The spectrum and prevalence of genetic pathology among the population of a certain region are determined by the founder effect and microevolution factors and, therefore, are not always comparable in different countries. The study of these indicators
Externí odkaz:
https://doaj.org/article/06e12aaabf1841da836c00b83b95da11
Autor:
Lilia Chorna, Pavlo Ryzhko, Vitalii Vorontsov, Halyna Makukh, Serhii Belyaev, Larysa Roshcheniuk, Olena Fedota, Iurii Sadovnychenko, Igor V. Belozorov, Ivanna Haybonyuk
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 9:291-297
BACKGROUND: Ichthyosis vulgaris is the most common type of Mendelian disorders of cornification, caused by loss-of-function mutations in the gene encoding epidermal protein filaggrin (FLG), namely R501X and 2282del4. FLG 2282del4 mutation in heterozy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::957750acc16df741a49b27ccaa0e7f71
https://doi.org/10.3889/oamjms.2021.6004
https://doi.org/10.3889/oamjms.2021.6004
Autor:
J. V. Gontar, P. P. Ryzhko, L. V. Roshcheniuk, Iurii Sadovnychenko, V. M. Vorontsov, Olena Fedota, I. M. Merenkova
Publikováno v:
Cytology and Genetics. 55:47-52
X-linked recessive ichthyosis (OMIM 308100) is a form of ichthyosis caused by abnormal keratinization and can result in disability, social maladaptation, and decreased quality of life for patients and their families. In most cases the disease is caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d05b1c1e4b9192b115b3bf882ac976a6
https://doi.org/10.3103/s0095452721010072
https://doi.org/10.3103/s0095452721010072
Autor:
Yana Hryshchenko, Mykola Hryshchenko, Iurii Sadovnychenko, Kostiantyn Tyshchenko, Olena Fedota
Publikováno v:
Actual problems of modern medicine.
The spectrum and prevalence of genetic pathology among the population of a certain region are determined by the founder effect and microevolution factors and, therefore, are not always comparable in different countries. The study of these indicators
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73cc6d4546796ce63760525bc52be506
https://doi.org/10.26565/2617-409x-2019-3-03
https://doi.org/10.26565/2617-409x-2019-3-03