Zobrazeno 1 - 6
of 6
pro vyhledávání: '"T.V. Usenko"'
Publikováno v:
Репродуктивная эндокринология, Iss 63-64, Pp 67-71 (2022)
This article presents a description of our own case of ultrasound prenatal diagnostics of complex combined heart disease (complete atrioventricular communication in combination with tetralogy of Fallot) at 19–20 weeks of gestation with ultrasound m
Externí odkaz:
https://doaj.org/article/f4eb9f9fcd644c39b1810a4b488e0ec5
Autor:
O.V. Reshavska, N.M. Nedopytanska, Ye.A. Bahlii, T.V. Usenko, L.V. Tkachenko, T.I. Kliuchynska, T.V. Verbova
Publikováno v:
Ukrainian Journal of Modern Toxicological Aspects. 92:68-83
The herbicide propisochlor is widely used in agriculture of Ukraine. Its intensive usage is potentially dangerous due to residues in agricultural products, ecosystems, as well as effects on animals’ and humans’ organisms. This fact necessitates t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3940a09356479d32f026e9b5a2c4d668
https://doi.org/10.33273/2663-4570-2022-92-1-68-83
https://doi.org/10.33273/2663-4570-2022-92-1-68-83
Autor:
T.P. Borysova, I.V. Tverdokhlib, O.Yu. Obolonska, A.S Korolenko, K.I. Diahovets, D.M. Surkov, T.V. Usenko
Publikováno v:
Morphologia. 15:28-38
Background. Kidney has protracted nephrogenesis and depend on hemodynamic changes on the highest level in support of natural transition to extrauterine circulation. Fetal communications like Ductus Arteriosus take part in the shunting from the aorta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56bd9ec0e92a354511fbfb983f3b4a11
https://doi.org/10.26641/1997-9665.2021.1.28-38
https://doi.org/10.26641/1997-9665.2021.1.28-38
Publikováno v:
prenatal diagnosis.
Apert syndrome is a rare monogenic autosomal dominant disorder characterized by severe craniosynostosis, hypoplastic mediofacial structures and symmetric syndactyly of the upper and lower limbs. De novo case with Apert synclrome fetus was detected pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5ba64d7e0c15585fd1e9d3bcb1bdfe2
https://doi.org/10.21516/2413-1458-2018-17-2-134-140
https://doi.org/10.21516/2413-1458-2018-17-2-134-140
Publikováno v:
prenatal diagnosis.
Meckel — Gruber syndrome (MGS) is a rare lethal autosomal recessive disorder characterised by occipital encephalocele, polydactyly and bilateral dysplastic cystic kidneys. A case of prenatal diagnosis of MGS at 12 weeks of gestation is described. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d19848b52edb19b50bf2560bf354a0c
https://doi.org/10.21516/2413-1458-2018-17-1-62-67
https://doi.org/10.21516/2413-1458-2018-17-1-62-67
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.