Výsledky vyhledávání - "E.V. KUDRYAVTSEVA"

THE METHODOLOGY OF TEACHING CIVIL PROCEDURE (MEMORIES OF MIKHAIL KONSTANTINOVICH TREUSHNIKOV)

Autor: E.V. KUDRYAVTSEVA

Publikováno v: Herald of Civil Procedure. 11:22-33

The article is dedicated to the memory of Mikhail Konstantinovich Treushnikov, Doctor of Law, Professor, Honored Scientist, Head of the Department of Civil Procedure of the Law Faculty of the Lomonosov Moscow State University. The article analyzes th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8e4e95de342d8929f7dc0bbf7c273e5a
https://doi.org/10.24031/2226-0781-2021-11-5-22-33

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Late diagnosis of complete androgen insensitivity syndrome: Case report

Autor: E.V. Kudryavtseva, V.V. Kovalev, A.V. Geets, O.V. Patsyuk

Publikováno v: Sexologies. 30:e119-e123

Summary Objective To demonstrate a case of late detection of complete androgen insensitivity syndrome (CAIS). Case report A case of CAIS is presented, which was identified in a patient at 32 years old. A complete general examination was carried out.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dff591418c517e01375cc02cb492c5fd
https://doi.org/10.1016/j.sexol.2021.06.007

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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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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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