Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Oleksii Khaniukov"'
Publikováno v:
Journal of V. N. Karazin Kharkiv National University: Series Medicine, Vol 43, Pp 40-48 (2021)
As a permanent blockage of the pathogenetic chains of the disease prevents its progression and decompensation, medication adherence remains a cornerstone in the management of chronic heart failure. Poor adherence leads to an increase in chronic heart
Externí odkaz:
https://doaj.org/article/96303e1c5623489b857965cb3972c06e
Autor:
Oleksii Khaniukov, Valerii Chornyi, Ihor Yevstihnieiev, Ihor Hutnik, Oleksandra Smolianova, Nataliia Romuz, Kateryna Esterkina, Kateryna Pervieieva
Publikováno v:
Journal of V. N. Karazin Kharkiv National University: Series Medicine, Vol 41, Pp 115-122 (2021)
Background. Lesch-Nyhan syndrome is inherent X-linked recessive genetic disorder with decreased activity of hypoxanthine-guanine phosphoribosyltransferase (HGPRT). The disease is characterized by presence of the classical triad: hyperuricemia, neurol
Externí odkaz:
https://doaj.org/article/e1ff0e65a17c4914bd65645e208c3d6a
Autor:
Oleksii Khaniukov
Publikováno v:
Ukraïnsʹkij žurnal medicini, bìologìï ta sportu. 7:76-82
The purpose of the study was to evaluate hemodynamic changes in middle-aged and older patients with coronary artery disease and anemia, against the background of standard therapy, as well as in combination with L-arginine. Materials and methods. 53 p
Background: Comorbidities and sex differences play a major role in chronic heart failure (CHF). However, it is unknown whether the prevalence of comorbidities differs between heart failure with preserved ejection fraction, mildly reduced ejection fra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef8165ff9ec4a23d81d6078447c5271e
https://doi.org/10.21203/rs.3.rs-2770634/v1
https://doi.org/10.21203/rs.3.rs-2770634/v1
Autor:
Ihor Hutnik, Oleksandra Smolianova, Kateryna Esterkina, Kateryna Pervieieva, Oleksii Khaniukov, Valerii Chornyi, Ihor Yevstihnieiev, Nataliia Romuz
Publikováno v:
Journal of V. N. Karazin Kharkiv National University: Series Medicine, Vol 41, Pp 115-122 (2021)
Background. Lesch-Nyhan syndrome is inherent X-linked recessive genetic disorder with decreased activity of hypoxanthine-guanine phosphoribosyltransferase (HGPRT). The disease is characterized by presence of the classical triad: hyperuricemia, neurol
Publikováno v:
Women's Health. 7:96-102
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a5b5fc562967a2102c7c96039a4b930f
http://www.scopus.com/inward/record.url?eid=2-s2.0-85059245427&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85059245427&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::abb75d9a037e95afcdc83354d7703874
http://www.scopus.com/inward/record.url?eid=2-s2.0-85046267672&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-85046267672&partnerID=MN8TOARS