Zobrazeno 1 - 10 of 49 pro vyhledávání: '"I.V. Kanivets"'
1
The role of fetal chromosomal aberrations in the genesis of recurrent and sporadic miscarriage
Autor: S.A. Korostelev, V.V. Kovalev, Yu.K. Kievskaya, Perinatology named after Academician V.I.Kulakov, Moscow, Russian Federation, 'Genomed' Llc, Moscow, Russian Federation, I.I.Baranov I.I.Baranov, E.V. Kudryavtseva, I.V. Kanivets, N. N. Potapov
Publikováno v: Voprosy ginekologii, akušerstva i perinatologii. 20:34-39
Objective. To compare the frequency and nature of embryo/fetus chromosomal abnormalities (CA) in sporadic and recurrent pregnancy loss. Patients and methods. A retrospective cohort study that included 1000 patients with pregnancy loss at 6–12 weeks
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::63cee9bf7ccbd9f23ad262bc6b8e7550
https://doi.org/10.20953/1726-1678-2021-1-34-39
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2
The use of chromosomal microarray analysis for diagnostics of chromosomal pathology in fetal central nervous system malformations
Autor: I.V. Kanivets, Denis V Pyankov, J. K. Kievskaya, E.V. Kudryavtseva, S.A. Korostelev
Publikováno v: Акушерство, гинекология и репродукция, Vol 14, Iss 4, Pp 449-456 (2020)
Introduction. The prevalence of congenital malformations (CMFs) in fetal central nervous system (CNS) ranges from 1.5 to 3 % and covers around 29 % among all malformations, whereas percentage in the structure of perinatal and infant mortality reaches
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c74a07a66efa53d9b6320b00bd1755c4
https://doi.org/10.17749/2313-7347/ob.gyn.rep.2020.160
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4
Low Fetal Fraction of Cell-free DNA Identified by Non-invasive Prenatal DNA Testing: Possible Causes, Clinical Significance, and Tactics
Autor: E.V. Kudryavtseva, V.V. Kovalev, S.A. Korostelev, Russian Federation Moscow, I.I.Baranov I.I.Baranov, Yu.K. Kievskaya, Russian Federation Ekaterinburg, Ooo Genomed, I.V. Kanivets
Publikováno v: Doctor.Ru. 19:49-54
Study Objective: To compare the rates of fetal chromosomal abnormalities (CA) detected during initial non-invasive prenatal DNA testing (NIPT) with the rates of CA found through repeat NIPT in patients with low fetal fraction or low quality of cell-f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5a3db21e3d78e7ef91af475c3fb4fed7
https://doi.org/10.31550/1727-2378-2020-19-8-49-54
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9
SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold
Autor: J.K. Kievskaya, N.V. Shilova, I.V. Kanivets, E.V. Kudryavtseva, D.V. Pyankov, S.A. Korostelev
Publikováno v: Sovremennye tekhnologii v meditsine. 13(6)
The study included 225 pregnant women who underwent invasive prenatal diagnostic procedures following the detection of an isolated thickening of the fetal nuchal fold. The fetal material obtained was examined using a cytogenetic test; if a normal kar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda9203ed6e3ba28f83ca7c3b3c10c69
https://pubmed.ncbi.nlm.nih.gov/35265361
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