Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Olena Fedota"'
Autor:
Valeriia Dorofieieva, Olena Fedota
Publikováno v:
Journal of V. N. Karazin Kharkiv National University: Series Medicine, Vol 45, Iss 45, Pp 24-36 (2022)
Introduction. The relevance of the study of genetic pathologies is due to the growing prevalence in most countries, disability and mortality of persons, high costs of support and treatment. The modern classifications include various forms of porphyri
Externí odkaz:
https://doaj.org/article/c69c8af2d37146f58ec4b84a6ff852cb
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:
Olena Fedota, Nina Puzik, Inessa Skrypkina, Volodymyr Babalyan, Larysa Mitiohlo, Serhii Ruban, Serhii Belyaev, Oleksandr O. Borshch, Oleksandr V. Borshch
Publikováno v:
Acta Biologica Szegediensis. 66:7-15
The chronic consumption of mycotoxin-contaminated forage tends to the weight loss of young cattle, decreasing the reproductive success of adult animals, milk yield, and tolerance to high temperatures. The aim of this paper was to study the eff ects o
Autor:
Olena Fedota
Publikováno v:
Ukraïnsʹkij žurnal medicini, bìologìï ta sportu. 7:120-126
The purpose of the study was to ilustrate the analysis of etiological factors of liver cirrhosis using clinical and anamnestic data and the results of instrumental, laboratory and genetic researches. Materials and methods. The data of anamnesis and o
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
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 9:1-5
INTRODUCTION: According to the data by World Health Organization, the broad and often insufficiently substantiated prescription of antibiotics, including for prophylactic purposes, has led to the growth of antibiotic-resistant microflora, which is a
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
Autor:
Galina Gubina-Vakulik, Sergei G. Belyaev, Olena Fedota, Iryna S. Belyaeva, Natalia S. Nestertsova, Olena V. Doroganova
Publikováno v:
Wiadomości Lekarskie. 74:190-195
Objective The aim: Study of the functional morphology of placenta in a sedentary lifestyle of a woman during pregnancy. Patients and methods Materials and methods: Object of the study: placentas obtained as a result of deliveries at term from women,
Autor:
V. M. Vorontsov, N. G. Puzik, T. V. Tyzhnenko, L. V. Roschenyuk, Kharkiv Regional Clinical Skin, Olena Fedota, P. P. Ryzhko
Publikováno v:
Ukrainian Biochemical Journal, Vol 92, Iss 1, Pp 66-74 (2020)
Methotrexate (MTX) is the immunosuppressive anti-inflammatory drug and the antagonist of the enzyme dihydrofolate reductase. Pharmacogenomic studies and clinical evidences suggest that altered response to MTX in patients with different diseases is as
Publikováno v:
ScienceRise: Medical Science, Vol 0, Iss 4 (37), Pp 29-33 (2020)
About 75 % of the world’s population loses ability to lactose tolerance in adulthood. The study of tolerance to lactose (LT) or lactase persistence (LP) in Ukrainians is necessary to identify the association of this trait with multifactorial pathol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ac15cf6437a8f9760feca7d50596cdc
https://zenodo.org/record/3971676
https://zenodo.org/record/3971676