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1Academic Journal
Πηγή: Высшая школа: научные исследования.
Θεματικοί όροι: гиперактивация сперматозоидов, интрацитоплазматическая инъекция сперматозоида, кофеин, вспомогательные репродуктивные технологии, экстракорпоральное оплодотворение, подвижность сперматозоидов
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2Academic Journal
Συγγραφείς: Prikulis J., Stepanyan L.G., Sagurova Y.M., Komarova E.M., Lesik E.A., Dzhemlikhanova L.K., Niauri D.A., Borovets S.Y., Gzgzyan A.M., Kogan I.Y.
Πηγή: Marine Medicine; Vol 10, No 4 (2024); 26-32 ; Морская медицина; Vol 10, No 4 (2024); 26-32 ; 2587-7828 ; 2413-5747
Θεματικοί όροι: marine medicine, spermogram, sperm motility, in vitro fertilization, intracytoplasmic sperm injection, clinical pregnancy, live birth, assisted reproductive technologies, морская медицина, спермограмма, подвижность сперматозоидов, экстракорпоральное оплодотворение, интрацитоплазматическая инъекция сперматозоида, клиническая беременность, живорождение, вспомогательные репродуктивные технологии
Περιγραφή αρχείου: application/pdf
Relation: https://seamed.bmoc-spb.ru/jour/article/view/774/676; GXEHOJ
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3Academic Journal
Συγγραφείς: I. S. Krysanov, V. S. Krysanova, V. Yu. Ermakova, И. С. Крысанов, В. С. Крысанова, В. Ю. Ермакова
Πηγή: FARMAKOEKONOMIKA. Modern Pharmacoeconomics and Pharmacoepidemiology; Vol 16, No 2 (2023); 221-235 ; ФАРМАКОЭКОНОМИКА. Современная фармакоэкономика и фармакоэпидемиология; Vol 16, No 2 (2023); 221-235 ; 2070-4933 ; 2070-4909
Θεματικοί όροι: анализ влияния на бюджет, follitropin alfa, assisted reproductive technologies, ART, in vitro fertilization, IVF, intracytoplasmic sperm injection, ICSI, cost-effectiveness analysis, budget impact analysis, фоллитропин альфа, вспомогательные репродуктивные технологии, ВРТ, экстракорпоральное оплодотворение, ЭКО, интрацитоплазматическая инъекция сперматозоида, ИКСИ, анализ «затраты–эффективность»
Περιγραφή αρχείου: application/pdf
Relation: https://www.pharmacoeconomics.ru/jour/article/view/828/473; Кулаков В.И., Назаренко Т.А., Тер-Аванесов Г.В. Бесплодный брак: достижения, проблемы, перспективы. Тезисы конференции «Мужское здоровье»; 2003.; Mascarenhas M.N., Flaxman S.R., Boerma T., et al. National, regional, and global trends in infertility prevalence since 1990: a systematic analysis of 277 health surveys. PLoS Med. 2012; 9 (12): e1001356. https://doi.org/10.1371/journal.pmed.1001356.; Boivin J., Bunting L., Collins J.A., et al. International estimates of infertility prevalence and treatment-seeking: potential need and demand for infertility medical care. Hum Reprod. 2007; 22 (6): 1506–12. https://doi.org/10.1093/humrep/dem046.; Rutstein S.O., Shah I.H. Infecundity infertility and childlessness in developing countries. URL: https://dhsprogram.com/pubs/pdf/CR9/CR9.pdf (дата обращения 03.03.2023).; Устинова Т.А., Артымук Н.В., Власова В.В., Пыжов А.Я. Бесплодие в Кемеровской области. Мать и дитя в Кузбассе. 2010; 1: 37–9.; Ринчиндоржиева М.П., Колесников С.И., Сутурина Л.В. и др. Эпидемиология женского бесплодия городского населения Республики Бурятия. Бюллетень Восточно-Сибирского научного центра Сибирского отделения Российской академии медицинских наук. 2011; 4-2: 295–8.; Фролова Н.И., Белокриницкая Т.Е., Анохова Л.И. и др. Распространенность и характеристика бесплодия у женщин молодого фертильного возраста Забайкальского края. Бюллетень Восточно-Сибирского научного центра Сибирского отделения Российской академии медицинских наук. 2014; 4: 54–8.; Литвинова Е.В., Носкова О.В., Былым Г.В. О клинических и демографических аспектах бесплодия и путях преодоления его последствий. Вестник гигиены и эпидемиологии. 2021; 25 (2): 196–202.; De Geyter C., Wyns C., Calhaz-Jorge C., et al. 20 years of the European IVF-monitoring Consortium registry: what have we learned? A comparison with registries from two other regions. Hum Reprod. 2020; 35 (12): 2832–49. https://doi.org/10.1093/humrep/deaa250.; Российская ассоциация репродукции человека. Регистр ВРТ: отчет за 2020 г. URL: https://www.rahr.ru/d_registr_otchet/RegistrVRT_2020.pdf (дата обращения 03.03.2023).; Федеральный проект «Финансовая поддержка семей при рождении детей». URL: https://mintrud.gov.ru/ministry/programms/demography/1 (дата обращения 03.03.2023).; Калугина А.А., Боярский К.Ю., Маколкин А.А. и др. Обзор результатов клинических исследований фоллитропина дельта в протоколах овариальной стимуляции. Первый опыт применения в России. Акушерство и гинекология. 2021; 11: 246–64. https://doi.org/10.18565/aig.2021.11.246-264.; Busso C., Soares S., Pellicer A. (2019) Pathogenesis, clinical manifestations, and diagnosis of ovarian hyperstimulation syndrome. URL: https://www.uptodate.com/contents/pathogenesis-clinical-manifestations-and-diagnosis-of-ovarian-hyperstimulation-syndrome (дата обращения 03.02.2023).; Государственный реестр лекарственных средств. Официальная инструкция по применению лекарственного препарата Рековелль®. URL: https://grls.rosminzdrav.ru/grls.aspx (дата обращения 17.02.2023).; Methley A.M., Campbell S., Chew-Graham C., et al. PICO, PICOS and SPIDER: a comparison study of specificity and sensitivity in three search tools for qualitative systematic reviews. BMC Health Serv Res. 2014; 14: 579. https://doi.org/10.1186/s12913-014-0579-0.; Nyboe Andersen A., Nelson S.M., Fauser B.C., et al. Individualized versus conventional ovarian stimulation for in vitro fertilization: a multicenter, randomized, controlled, assessor-blinded, phase 3 noninferiority trial. Fertil Steril. 2017; 107 (2): 387–96.e4. https://doi.org/10.1016/j.fertnstert.2016.10.033.; Bosch E., Havelock J., Martin F.S., et al. Follitropin delta in repeated ovarian stimulation for IVF: a controlled, assessor-blind Phase 3 safety trial. Reprod Biomed Online. 2019; 38 (2): 195–205. https://doi.org/10.1016/j.rbmo.2018.10.012.; Fernández-Sánchez M., Visnova H., Yuzpe A., et al. Individualization of the starting dose of follitropin delta reduces the overall OHSS risk and/or the need for additional preventive interventions: cumulative data over three stimulation cycles. Reprod Biomed Online. 2019; 38 (4): 528–37. https://doi.org/10.1016/j.rbmo.2018.12.032.; Ягудина Р.И., Сороковиков И.В. Методология проведения анализа «затраты-полезность» при проведении фармакоэкономических исследований. ФАРМАКОЭКОНОМИКА Современная фармакоэкономика и фармакоэпидемиология. 2012; 5 (2): 9–12.; Омельяновский В.В., Авксентьева М.В., Хачатрян Г.Р. и др. Методические рекомендации по использованию математического моделирования в клинико-экономических исследованиях и исследованиях с использованием анализа влияния на бюджет. М.: ФГБУ «ЦЭККМП» Минздрава России»; 2019: 59 с.; Государственный реестр лекарственных средств. URL: https://grls.rosminzdrav.ru/Default.aspx (дата обращения 27.01.2023).; Методические рекомендации по способам оплаты медицинской помощи за счет средств обязательного медицинского страхования. URL: https://www.ffoms.gov.ru/upload/iblock/e60/e60ae170a1b14490d9f2315f77e37304.pdf (дата обращения 07.02.2023).; Постановление Правительства РФ от 29.12.2022 № 2497 «О Программе государственных гарантий бесплатного оказания гражданам медицинской помощи на 2023 год и на плановый период 2024 и 2025 годов». URL: http://publication.pravo.gov.ru/Document/View/0001202212310044 (дата обращения 23.01.2023).; Омельяновский В.В., Авксентьева М.В., Сура М.В. и др. Методические рекомендации по проведению сравнительной клинико-экономической оценки лекарственного препарата (новая редакция). М.: ФГБУ «ЦЭККМП»; 2018.; https://www.pharmacoeconomics.ru/jour/article/view/828
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4Academic Journal
Συγγραφείς: Yu. V. Olefir, E. A. Efremov, M. A. Rodionov, A. R. Zhuvilko, D. M. Popov, D. M. Monakov, Ю. В. Олефир, Е. А. Ефремов, М. А. Родионов, А. Р. Живулько, Д. М. Попов, Д. М. Монаков
Πηγή: Andrology and Genital Surgery; Том 24, № 4 (2023); 67-72 ; Андрология и генитальная хирургия; Том 24, № 4 (2023); 67-72 ; 2412-8902 ; 2070-9781
Θεματικοί όροι: внутриматочная инсеминация, male infertility, in vitro fertilization, intracytoplasmic sperm injection, intrauterine insemination, мужское бесплодие, экстракорпоральное оплодотворение, интрацитоплазматическая инъекция сперматозоида
Περιγραφή αρχείου: application/pdf
Relation: https://agx.abvpress.ru/jour/article/view/706/551; Krawetz S.A. Paternal contribution: new insights and future challenges. Nat Revi Genet 2005;6(8):633–42. DOI:10.1038/nrg1654; Рогозин Д.С. Мужская фертильность: обзор литературы января – марта 2021 года. Вестник урологии 2021;9(2):142–9. DOI:10.21886/2308-6424-2021-9-2-142-149; Коршунов М.Н., Коршунова Е.С., Кызласов П.С. и др. Структурные нарушения хроматина сперматозоидов. Патофизиологические аспекты. Клиническая значимость. Вестник урологии 2021;9(1):95–104. DOI:10.21886/2308-6424-2021-9-1-95-104; Руднева С.А., Брагина Е.Е., Арифулин Е.А. и др. Фрагментация ДНК в сперматозоидах и ее взаимосвязь с нарушением сперматогенеза. Андрология и генитальная хирургия 2014;15(4):26–33. DOI:10.17650/2070-9781-2014-4-26-33; Рыжков А.И., Шорманов И.С., Соколова С.Ю. Фрагментация ДНК сперматозоидов. Есть ли связь с основными параметрами спермы и возрастом? Экспериментальная и клиническая урология 2020;(4):58–64. DOI:10.29188/2222-8543-2020-13-4-58-64; Авадиева Н.Э. Применение ДНК фрагментации спермы в андрологической практике. Вестник урологии 2019;7(1):7–11. DOI:10.21886/2308-6424-2019-7-1-7-11; Agarwal A., Majzoub A., Esteves S.C. et al. Clinical utility of sperm DNA fragmentation testing: practice recommendations based on clinical scenarios. Transl Androl Urol 2016;5(6):935–50. DOI:10.21037/tau.2016.10.03; Aitken R.J. Oxidative stress and the etiology of male infertility. J Assist Reprod Genet 2016;33(12):1691–2. DOI:10.1007/s10815-016-0791-4; Aitken R.J. DNA damage in human spermatozoa; important contributor to mutagenesis in the offspring. Transl Androl Urol 2017;6(Suppl 4):S761–4. DOI:10.21037/tau.2017.09.13; Bui A.D., Sharma R., Henkel R., Agarwal A. Reactive oxygen species impact on sperm DNA and its role in male infertility. Andrologia 2018;50(8):e13012. DOI:10.1111/and.13012; Esteves S.C., Gosálvez J., López-Fernández C. et al. Diagnostic accuracy of sperm DNA degradation index (DDSi) as a potential noninvasive biomarker to identify men with varicocele-associated infertility. Int Urol Nephrol 2015;47(9):1471–7. DOI:10.1007/s11255-015-1053-6; Rima D., Shiv B.K., Bhavna C. et al. Oxidative stress induced damage to paternal genome and impact of meditation and yoga – can it reduce incidence of childhood cancer? Asian Pac J Cancer Prev 2016;17(9):4517–25.; Коршунов М.Н., Коршунова Е.С., Даренков С.П. Клиническая эффективность использования тестикулярных сперматозоидов в программах репродуктивных технологий при высоком показателе ДНК-фрагментации. Урологические ведомости 2017;7(5):57–8.; González-Marín C., Gosálvez J., Roy R. Types, causes, detection and repair of DNA fragmentation in animal and human sperm cells. Int J Mol Sci 2012;13(11):14026–52. DOI:10.3390/ijms131114026; Simon L., Brunborg G., Stevenson M. et al. Clinical significance of sperm DNA damage in assisted reproduction outcome. Hum Reprod 2010;25(7):1594–608. DOI:10.1093/humrep/deq103; Simon L., Emery B.R., Carrell D.T. Review: diagnosis and impact of sperm DNA alterations in assisted reproduction. Best Pract Res Clin Obstet Gynaecol 2017;44:38–56. DOI:10.1016/j.bpobgyn.2017.07.003; Simon L., Lutton D., McManus J., Lewis S.E. Sperm DNA damage measured by the alkaline Comet assay as an independent predictor of male infertility and in vitro fertilization success. Fertil Steril 2011;95(2):652–7. DOI:10.1016/j.fertnstert.2010.08.019; Simon L., Murphy K., Shamsi M.B. et al. Paternal influence of sperm DNA integrity on early embryonic development. Hum Reprod 2014;29(11):2402–12. DOI:10.1093/humrep/deu228; Simon L., Proutski I., Stevenson M. et al. Sperm DNA damage has a negative association with live-birth rates after IVF. Reprod BioMed Online 2013;26(1):68–78. DOI:10.1016/j.rbmo.2012.09.019; Santi D., Spaggiari G., Simoni M. Sperm DNA fragmentation index as a promising predictive tool for male infertility diagnosis and treatment management – meta-analyses. Reprod Biomed Online 2018;37(3):315–26. DOI:10.1016/j.rbmo.2018.06.023; Spanò M., Kolstad A.H., Larsen S.B. et al. The applicability of the flow cytometric sperm chromatin structure assay in epidemiological studies. Asclepios. Hum Reprod 1998;13(9):2495–505. DOI:10.1093/humrep/13.9.2495; Evenson D.P., Jost L.K., Marshall D. et al. Utility of the sperm chromatin structure assay as a diagnostic and prognostic tool in the human fertility clinic. Hum Reprod 1999;14(4):1039–49. DOI:10.1093/humrep/14.4.1039; Evenson D.P., Wixon R.L. Environmental toxicants cause sperm DNA fragmentation as detected by the Sperm Chromatin Structure Assay (SCSA®). Toxicol Appl Pharmacol 2005;207(2 Suppl):532–7. DOI:10.1016/j.taap.2005.03.021; Malić Vončina S., Golob B., Ihan A. et al. Sperm DNA fragmentation and mitochondrial membrane potential combined are better for predicting natural conception than standard sperm parameters. Fertil Steril 2016;105(3):637–44.e.1. DOI:10.1016/j.fertnstert.2015.11.037; Vandekerckhove F.W., De Croo I., Gerris J. et al. Sperm chromatin dispersion test before sperm preparation is predictive of clinical pregnancy in cases of unexplained infertility treated with intrauterine insemination and induction with clomiphene citrate. Front Med (Lausanne) 2016;3:63. DOI:10.3389/fmed.2016.00063; Bungum M., Humaidan P., Axmon A. et al. Sperm DNA integrity assessment in prediction of assisted reproduction technology outcome. Hum Reprod 2007;22(1):174–9. DOI:10.1093/humrep/del326; Bungum M., Humaidan P., Spano M. et al. The predictive value of sperm chromatin structure assay (SCSA) parameters for the outcome of intrauterine insemination, IVF and ICSI. Hum Reprod 2004;19(6):1401–8. DOI:10.1093/humrep/deh280; Duran E.H., Morshedi M., Taylor S., Oehninger S. Sperm DNA quality predicts intrauterine insemination outcome: a prospective cohort study. Hum Reprod 2002;17(12):3122–8. DOI:10.1093/humrep/17.12.3122; Rilcheva V.S., Ayvazova N.P., Ilieva L.O. et al. Sperm DNA integrity test and assisted reproductive technology (Art) outcome. J Biomed Clin Res 2016;9:21–9. DOI:10.1515/jbcr-2016-0003; Chen Q., Zhao J.Y., Xue X., Zhu G.X. The association between sperm DNA fragmentation and reproductive outcomes following intrauterine insemination, a meta-analysis. Reprod Toxicol 2019;86:50–5. DOI:10.1016/j.reprotox.2019.03.004; Sugihara A., Van Avermaete F., Roelant E. et al. The role of sperm DNA fragmentation testing in predicting intra-uterine insemination outcome: a systematic review and meta-analysis. Eur J Obstet Gynecol Reprod Biol 2020;244:8–15. DOI:10.1016/j.ejogrb.2019.10.005; Li Z., Wang L., Cai J., Huang H. Correlation of sperm DNA damage with IVF and ICSI outcomes: a systematic review and meta-analysis. J Assist Reprod Genet 2006;23(9–10):367–76. DOI:10.1007/s10815-006-9066-9; Zhao J., Zhang Q., Wang Y., Li Y. Whether sperm deoxyribonucleic acid fragmentation has an effect on pregnancy and miscarriage after in vitro fertilization/intracytoplasmic sperm injection: a systematic review and meta-analysis. Fertil Steril 2014;102(4):998–1005e.8. DOI:10.1016/j.fertnstert.2014.06.033; Osman A., Alsomait H., Seshadri S. et al. The effect of sperm DNA fragmentation on live birth rate after IVF or ICSI: a systematic review and meta-analysis. Reprod Biomed Online 2015;30:120–7. DOI:10.1016/j.rbmo.2014.10.018; Deng C., Li T., Xie Y. et al. Sperm DNA fragmentation index influences assisted reproductive technology outcome: a systematic review and meta-analysis combined with a retrospective cohort study. Andrologia 2019;51(6):e13263. DOI:10.1111/and.13263; Lewis S.E.M. The place of sperm DNA fragmentation testing in current day fertility management. Middle East Fertil Soc J 2013;18(2):78–82. DOI:10.1016/j.mefs.2013.01.010; Meseguer M., Santiso R., Garrido N. et al. Effect of sperm DNA fragmentation on pregnancy outcome depends on oocyte quality. Fertil Steril 2011;95(1):124–8. DOI:10.1016/j.fertnstert.2010.05.055; Zini A., Jamal W., Cowan L., Al-Hathal N. Is sperm DNA damage associated with IVF embryo quality? A systematic review. J Assist Reprod Genet 2011;28(5):391–7. DOI:10.1007/s10815-011-9544-6; Moskovtsev S.I., Jarvi K., Mullen J.B. et al. Testicular spermatozoa have statistically significantly lower DNA damage compared with ejaculated spermatozoa in patients with unsuccessful oral antioxidant treatment. Fertil Steril 2010;93(4):1142–6. DOI:10.1016/j.fertnstert.2008.11.005; Greco E., Scarselli F., Iacobelli M. et al. Efficient treat ment of infertility due to sperm DNA damage by ICSI with testicular spermatozoa. Hum Reprod 2005;20(1):226–30. DOI:10.1093/humrep/deh590; Arafa M., AlMalki A., AlBadr M. et al. ICSI outcome in patients with high DNA fragmentation: testicular versus ejaculated spermatozoa. Andrologia 2018;50(1). DOI:10.1111/and.12835; Zhang J., Xue H., Qiu F. et al. Testicular spermatozoon is superior to ejaculated spermatozoon for intracytoplasmic sperm injection to achieve pregnancy in infertile males with high sperm DNA damage. Andrologia 2019;51(2):e13175. DOI:10.1111/and.13175; Pabuccu E.G., Caglar G.S., Tangal S. et al. Testicular versus ejaculated spermatozoa in ICSI cycles of nor mozoospermic men with high sperm DNA fragmen tation and previous ART failures. Andrologia 2017;49(2). DOI:10.1111/and.12609; Hayden R.P., Wright D.L., Toth T.L., Tanrikut C. Selective use of percutaneous testis biopsy to optimize IVF-ICSI outcomes: a case series. Fertil Res Pract 2016;2:7. DOI:10.1186/s40738-016-0020-y; Esteves S.C., Sánchez-Martín F., Sánchez-Martín P. et al. Comparison of reproductive outcome in oligozoospermic men with high sperm DNA fragmentation undergoing intracytoplasmic sperm injection with ejaculated and testicular sperm. Fertil Steril 2015;104(6):1398–405. DOI:10.1016/j.fertnstert.2015.08.028; Mehta A., Bolyakov A., Schlegel P.N., Paduch D.A. Higher pregnancy rates using testicular sperm in men withsevere oligospermia. Fertil Steril 2015;104(6):1382–7. DOI:10.1016/j.fertnstert.2015.08.008; Bradley C.K., McArthur S.J., Gee A.J. et al. Intervention improves assisted conception intracytoplasmic sperm injection outcomes for patients with high levels of sperm DNA fragmentation: a retrospective analysis. Andrology 2016;4(5):903–10. DOI:10.1111/andr.12215; Alharbi M., Hamouche F., Phillips S. et al. Use of testicular sperm in couples with SCSA-defined high sperm DNA fragmentation and failed intracytoplasmic sperm injection using ejaculated sperm. Asian J Androl 2020;22(4):348–53. DOI:10.4103/aja.aja_99_19; Esteves S.C., Roque M., Bradley C.K., Garrido N. Reproductive outcomes of testicular versus ejaculated sperm for intracytoplasmic sperm injection among men with high levels of DNA fragmentation in semen: systematic review and meta-analysis. Fertil Steril 2017;108(3):456–67.e1. DOI:10.1016/j.fertnstert.2017.06.018.; https://agx.abvpress.ru/jour/article/view/706
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5Academic Journal
Συγγραφείς: N. P. Naumov, T. V. Shatylko, S. I. Gamidov, A. Y. Popova, R. I. Safiullin, Н. П. Наумов, Т. В. Шатылко, С. И. Гамидов, А. Ю. Попова, Р. И. Сафиуллин
Πηγή: Andrology and Genital Surgery; Том 23, № 3 (2022); 61-71 ; Андрология и генитальная хирургия; Том 23, № 3 (2022); 61-71 ; 2412-8902 ; 2070-9781
Θεματικοί όροι: время разжижения, assisted reproductive technologies, intracytoplasmic sperm injection, sperm agglutination, dilution time, вспомогательные репродуктивные технологии, интрацитоплазматическая инъекция сперматозоида, агглютинация сперматозоидов
Περιγραφή αρχείου: application/pdf
Relation: https://agx.abvpress.ru/jour/article/view/586/474; Jo J., Lee S.H., Lee J.M., Jerng U.M. Semen quality improvement in a man with idiopathic infertility treated with traditional Korean medicine: a case report. Explore (NY) 2015;11(4):320–3. DOI:10.1016/j.explore.2015.04.007; Hamada A., Esteves S.C., Nizza M., Agarwal A. Unexplained male infertility: diagnosis and management. Int Braz J Urol 2012;38(5):576–94. DOI:10.1590/s1677-55382012000500002; Kumar R. Male infertility – current concepts. Indian J Urol 2011;21(1):39–40. DOI:10.4103/0970-1591.78419; Nicolau P., Miralpeix E., Solà I. et al. Alcohol consumption and in vitro fertilization: a review of the literature. Gynecol Endocrinol 2014;30(11):759–63. DOI:10.3109/09513590.2014.938623; Sanchez M., Aran B., Blanco J. et al. Preliminary clinical and FISH results on hyaluronic acid sperm selection to improve ICSI. Hum Reprod 2005;20:i200. Available at: https://www.researchgate.net/publication/285075274_Preliminary_clinical_and_FISH_results_on_hyaluronic_acid_sperm_selection_to_improve_ICSI (access date: 22.05.2022).; Artini P.G., Obino M.E., Carletti E. et al. Conventional IVF as a laboratory strategy to rescue fertility potential in severe poor responder patients: the impact of reproductive aging. Gynecol Endocrinol 2013;29(11):997–1001. DOI:10.3109/09513590.2013.822063; Gupta S., Sharma R., Agarwal A. Antisperm antibody testing: a comprehensive review of its role in the management of immunological male infertility and results of a global survey of clinical practices. World J Mens Health 2022;40(3):380–98. DOI: 0.5534/wjmh.210164; Vazquez-Levin M.H., Marín-Briggiler C.I., Veaute C. Antisperm antibodies: invaluable tools toward the identification of sperm proteins involved in fertilization. Am J Reprod Immunol 2014;72(2):206–18. DOI:10.1111/aji.12272; Mazumdar S., Levine A.S. Antisperm antibodies: etiology, pathogenesis, diagnosis, and treatment. Fertil Steril 1998;70(5):799–810. DOI:10.1016/s0015-0282(98)00302-1; Restrepo B., Cardona-Maya W. [Antisperm antibodies and fertility association (In Spanish)]. Actas Urol Esp 2013;37(9):571–8. DOI:10.1016/j.acuro.2012.11.003; Kaur G., Thompson L.A., Dufour J.M. Sertoli cells – immunological sentinels of spermatogenesis. Semin Cell Dev Biol 2014;30:36–44. DOI:10.1016/j.semcdb.2014.02.011; Francavilla F., Santucci R., Barbonetti A., Francavilla S. Naturally-occurring antisperm antibodies in men: interference with fertility and clinical implications. An update. Front Biosci 2007;12(8):2890–911. DOI:10.2741/2280; Lombardo F., Gandini L., Dondero F., Lenzi A. Immunology and immunopathology of the male genital tract: antisperm immunity in natural and assisted reproduction. Hum Reprod Update 2001;7(5):450–6. DOI:10.1093/humupd/7.5.450; Dimitrov D.G., Urbánek V., Zvĕrina J. et al. Correlation of asthenozoospermia with increased antisperm cell-mediated immunity in men from infertile couples. J Reprod Immunol 1994;27(1):3–12. DOI:10.1016/0165-0378(94)90011-6; Verón G.L., Molina R.I., Tissera A.D. Incidence of sperm surface autoantibodies and relationship with routine semen parameters and sperm kinematics. Am J Reprod Immunol 2016;76(1):59–69. DOI:10.1111/aji.12519; Gopalkrishnan K., Padwal V., Balaiah D. Does seminal fluid viscosity influence sperm chromatin integrity? Arch Androl 2000;45(2):99–103. DOI:10.1080/014850100418783; https://agx.abvpress.ru/jour/article/view/586
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6Academic Journal
Συγγραφείς: D. A. Doronicheva, N. S. Stuleva, Д. А. Дороничева, Н. С. Стулева
Πηγή: Obstetrics, Gynecology and Reproduction; Vol 14, No 2 (2020); 246-251 ; Акушерство, Гинекология и Репродукция; Vol 14, No 2 (2020); 246-251 ; 2500-3194 ; 2313-7347
Θεματικοί όροι: ГИФТ, IVF, assisted reproductive technologies, ART, intracytoplasmic sperm injection, ICSI, gamete intrafallopian tube transfer, GIFT, ЭКО, вспомогательные репродуктивные технологии, ВРТ, интрацитоплазматическая инъекция сперматозоида в ооцит, ИКСИ, перенос гамет в просвет маточной (фаллопиевой) трубы
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7Academic Journal
Συγγραφείς: V. V. Litvinov, A. N. Sulima, M. A. Kharitonova, A. A. Klepukov, I. Yu. Ermilova, Yu. Yu. Maclygina, В. В. Литвинов, А. Н. Сулима, М. А. Харитонова, А. А. Клепуков, И. Ю. Ермилова, Ю. Ю. Маклыгина
Πηγή: Andrology and Genital Surgery; Том 20, № 3 (2019); 78-85 ; Андрология и генитальная хирургия; Том 20, № 3 (2019); 78-85 ; 2412-8902 ; 2070-9781 ; 10.17650/2070-9781-2019-20-3
Θεματικοί όροι: клинический случай, Ca2+-ionophore, in vitro fertilization, intracytoplasmic sperm injection, intracytoplasmic morphologically normal sperm injection, pregnancy, clinical case, Ca2+-ионофор, экстракорпоральное оплодотворение, интрацитоплазматическая инъекция сперматозоида, интрацитоплазматическая инъекция морфологически нормального сперматозоида, беременность
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8Academic Journal
Συγγραφείς: A. V. Zobova, A. Kh. Dudarova, G. K. Sakharova, V. Yu. Smol'nikova, N. P. Makarova, А. В. Зобова, А. Х. Дударова, Г. К. Сахарова, В. Ю. Смольникова, Н. П. Макарова
Πηγή: Andrology and Genital Surgery; Том 16, № 4 (2015); 10-17 ; Андрология и генитальная хирургия; Том 16, № 4 (2015); 10-17 ; 2412-8902 ; 2070-9781 ; 10.17650/2070-9781-2015-16-4
Θεματικοί όροι: вспомогательные репродуктивные технологии, male infertility, hyaluronic acid, sperm selection, intracytoplasmic sperm injection, physiological intracytoplasmic sperm injection, assisted reproductive technologies, мужское бесплодие, гиалуроновая кислота, селекция сперматозоидов, интрацитоплазматическая инъекция сперматозоида, физиологическая интрацитоплазматическая инъекция сперматозоида
Περιγραφή αρχείου: application/pdf
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Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm. Hum Reprod 2010;25(10):2647–54.; Palermo G., Joris H., Devroey P., van Steirteghem A.C. Pregnancies after intracytoplasmic injection of single spermatozoon into an oocyte. Lancet 1992;340(8810):17–8.; Celik-Ozenci C., Jakab A., Kovacs T. et al. Sperm selection for ICSI: shape properties do not predict the absence or presence of numerical chromosomal aberrations. Hum Reprod 2004;19(9):2052–9.; Zini A., Finelli A., Phang D., Jarvi K. Influence of semen processing technique on human sperm DNA integrity. Urology 2000;56(6):1081–4.; Lucas H., Lammers J., Pfeffer J. et al. Conventional IVF versus ICSI in sibling oocytes: A French experience analysis for BLEFCO. Gynecol Obstet Fertil 2010;38(9):515–20.; Henkel R.R., Schill W.B. Sperm preparation for ART. Reprod Biol Endocrinol 2003;1:108.; A practical guide to select gametes and embryos. Ed.M. Montag. CRC Press, Taylor & Francis Group, 2014.; Parmegiani L., Cognigni G.E., Bernardi S. et al. “Physiologic ICSI”: hyaluronic acid (HA) favors selection of spermatozoa without DNA fragmentation and with normal nucleus, resulting in improvement of embryo quality. Fertil Steril 2010;93(2):598–604.; Suarez S.S., Pacey A.A. Sperm transport in the female reproductive tract. Hum Reprod Update 2006;12(1):23–37.; Aitken R., Bowie H., Buckingham D. et al. Sperm penetration into a hyaluronic acid polymer as a means of monitoring functional competence. J Androl 1992;13(1):44–54.; Cayli S., Jakab A., Ovari L. et al. Biochemical markers of sperm function: male fertility and sperm selection for ICSI. Reprod Biomed Online 2003;7(4):462–8.; Huszar G., Ozenci C.C., Cayli S. et al. Hyaluronic acid binding by human sperm indicates cellular maturity, viability, and unreacted acrosomal status. Fertil Steril 2003;79 Suppl 3:1616–24.; Huszar G., Stone K., Dix D., Vigue L. Putative creatine kinase M-isoform in human sperm is identified as the 70-kilodalton heat shock protein HspA2. Biol Reprod 2000;63(3):925–32.; Yeung C.H., Majumder G.C., Rolf C. et al. The role of phosphocreatine kinase in the motility of human spermatozoa supported by different metabolic substrates. Mol Hum Reprod 1996;2(8):591–6.; Huszar G., Celik-Ozenci C., Cayli S. et al. Semen characteristics after overnight shipping: preservation of sperm concentrations, HspA2 ratios, CK activity, cytoplasmic retention, chromatin maturity, DNA integrity, and sperm shape. J Androl 2004;25(4):593–604.; Jakab A., Sakkas D., Delpiano E. et al. Intracytoplasmic sperm injection: a novel selection method for sperm with normal frequency of chromosomal aneuploidies. Fertil Steril 2005;84(6):1665–73.; Huszar G., Jakab A., Sakkas D. et al. Fertility testing and ICSI sperm selection by hyaluronic acid binding: clinical and genetic aspects. Reprod Biomed Online 2007;14(5):650–63.; Nixon B., Aitken R.J. The biological significance of detergent-resistant membranes in spermatozoa. J Reprod Immunol 2009;83(1–2):8–13.; Gadella B.M. The assembly of a zona pellucida binding protein complex in sperm. Reprod Domest Anim 2008;43 Suppl 5:12–9.; Tanphaichitr N., Carmona E., Bou Khalil M. et al. New insights into spermzona pellucida interaction: involvement of sperm lipid rafts. Front Biosci 2007;12:1748–66.; Redgrove K.A., Anderson A.L., McLaughlin E. A. et al. Investigation of the mechanisms by which the molecular chaperone HSPA2 regulates the expression of sperm surface receptors involved in human sperm-oocyte recognition. Mol Hum Reprod 2013;19(3):120–35.; Redgrove K.A., Nixon B., Baker M.A. et al. The molecular chaperone HSPA2 plays a key role in regulating the expression of sperm surface receptors that mediate sperm-egg recognition. PLoS One 2012;7(11):e50851.; Motiei M., Tavalaee M., Rabiei F. et al. Evaluation of HSPA2 in fertile and infertile individuals. Andrologia 2013;45(1):66–72.; Evans E.A., Zhang H., Martin-DeLeon P.A. SPAM1(PH-20) protein and mRNA expression in the epididymides of humans and macaques: utilizing laser microdissection/ RT-PCR. Reprod Biol Endocrinol 2003;1:54.; Sabeur K., Cherr G.N., Yudin A.I. et al. The PH-20 protein in human spermatozoa. J Androl 1997;18(2):151–8.; Asquith K.L., Baleato R.M., McLaughlin E.A. et al. Tyrosine phosphorylation activates surface chaperones facilitating sperm-zona recognition. J Cell Sci 2004;117(Pt 16):3645–57.; Nixon B., Mitchell L.A., Anderson A.L. et al. Proteomic and functional analysis of human sperm detergent resistant membranes. J Cell Physiol 2011;226(10):2651–65.; Redgrove K.A., Anderson A.L., Dun M.D. et al. Involvement of multimeric protein complexes in mediating the capacitation-dependent binding of human spermatozoa to homologous zonae pellucidae. Dev Biol 2011;356(2):460–74.; Dun M.D., Smith N.D., Baker M.A. et al. The chaperonin containing TCP1 complex (CCT/TRiC) is involved in mediating sperm-oocyte interaction. J Biol Chem 2011;286(42):36875–87.; Kimura M., Kim E., Kang W. et al. Functional roles of mouse sperm hyaluronidases, HYAL5 and SPAM1, in fertilization. Biol Reprod 2009;81(5):939–47.; Lathrop W.F., Carmichael E.P., Myles D.G., Primakoff P. cDNA cloning reveals the molecular structure of a sperm surface protein, PH-20, involved in spermegg adhesion and the wide distribution of its gene among mammals. J Cell Biol 1990;111(6 Pt 2):2939–49.; Carmona E., Weerachatyanukul W., Soboloff T. et al. Arylsulfatase A is present on the pig sperm surface and is involved in sperm-zona pellucida binding. Dev Biol 2002;247(1):182–96.; Tantibhedhyangkul J., Weerachatyanukul W., Carmona E. et al. Role of sperm surface arylsulfatase A in mouse sperm – zona pellucida binding. Biol Reprod 2002;67(1):212–9.; Dix D.J., Allen J.W., Collins B.W. et al. HSP70-2 is required for desynapsis of synaptonemal complexes during meiotic prophase in juvenile and adult mouse spermatocytes. Development 1997;124(22):4595–603.; Osheroff J.E., Visconti P.E., Valenzuela J.P. et al. Regulation of human sperm capacitation by a cholesterol effluxstimulated signal transduction pathway leading to protein kinase A-mediated up-regulation of protein tyrosine phosphorylation. Mol Hum Reprod 1999;5(11):1017–26.; Cherr G.N., Yudin A.I., Overstreet J.W. The dual functions of GPI-anchored PH-20: hyaluronidase and intracellular signaling. Matrix Biol 2001;20(8):515–25.; Vandevoort C.A., Cherr G.N., Overstreet J.W. Hyaluronic acid enhances the zona pellucida-induced acrosome reaction of macaque sperm. J Androl 1997;18(1):1–5.; Sabeur K., Cherr G.N., Yudin A.I., Overstreet J.W. Hyaluronic acid enhances induction of the acrosome reaction of human sperm through interaction with the PH-20 protein. Zygote 1998;6(2):103–11.; Cherr G.N., Yudin A.I., Li M.W. et al. Hyaluronic acid and the cumulus extracellular matrix induce increases in intracellular calcium in macaque sperm via the plasma membrane protein PH-20. Zygote 1999;7(3):211–22.; Morales C.R., Badran H., El-Alfy M. et al. Cytoplasmic localization during testicular biogenesis of the murine mRNA for Spam1(PH-20), a protein involved in acrosomal exocytosis. Mol Reprod Dev 2004;69(4):475–82.; Ganguly A., Bansal P., Gupta T. et al. “ZP domain” of human zona pellucida glycoprotein-1 binds to human spermatozoa and induces acrosomal exocytosis. Reprod Biol Endocrinol 2010;8:110.; Hunnicutt G.R., Mahan K., Lathrop W.F. et al. Structural relationship of sperm soluble hyaluronidase to the sperm membrane protein PH-20. Biol Reprod 1996;54(6):1343–9.; Xu H., Liu F., Srakaew N. et al. Sperm arylsulfatase A binds to mZP2 and mZP3 glycoproteins in a nonenzymatic manner. Reproduction 2012;144(2): 209–19.; Reitinger S., Laschober G.T., Fehrer C. et al. Mouse testicular hyaluronidase-like proteins SPAM1 and HYAL5 but not HYALP1 degrade hyaluronan. Biochem J 2007;401(1):79–85.; Lin Y., Mahan K., Lathrop W.F. et al. A hyaluronidase activity of the sperm plasma membrane protein PH-20 enables sperm to penetrate the cumulus cell layer surrounding the egg. J Cell Biol 1994;125(5):1157–63.; Meyers S.A., Yudin A.I., Cherr G.N. et al. Hyaluronidase activity of macaque sperm assessed by an in vitro cumulus penetration assay. Mol Reprod Dev 1997;46(3):392–400.; Talbot P. Hyaluronidase dissolves a component in the hamster zona pellucida. J Exp Zool 1984;229(2):309–16.; Dandekar P., Talbot P. Perivitelline space of mammalian oocytes: extracellular matrix of unfertilized oocytes and formation of a cortical granule envelope following fertilization. Mol Reprod Dev 1992;31(2):135–43.; Yudin A.I., Li M.W., Robertson K.R. et al. Characterization of the active site of monkey sperm hyaluronidase. 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Spermatozoa bound to solid state hyaluronic acid show chromatin structure with high DNA chain integrity: an acridine orange fluorescence study. J Androl 2010;31(6):566–72.; Bartoov B., Berkovitz A., Eltes F. et al. Real-time fine morphology of motile human sperm cells is associated with IVF-ICSI outcome. J Androl 2002;23(1):1–8.; Cayli S., Sakkas D., Vigue L. et al. Cellular maturity and apoptosis in human sperm: creatine kinase, caspase-3 and Bcl-XL levels in mature and diminished maturity sperm. Mol Hum Reprod 2004;10(5):365–72.; Tarozzi N., Nadalini M., Bizzaro D. et al. Sperm-hyaluronan-binding assay: clinical value in conventional IVF under Italian law. Reprod Biomed Online 2009;19 Suppl 3:35–43.; Razavi S.H., Nasr-Esfahani M.H., Deemeh M.R. et al. Evaluation of zeta and HA-binding methods for selection of spermatozoa with normal morphology, protamine content and DNA integrity. Andrologia 2010;42(1):13–9.; Worrilow K.C., Eid S., Woodhouse D. et al. Use of hyaluronan in the selection of sperm for intracytoplasmic sperm injection (ICSI): significant improvement in clinical outcomes – multicenter, double-blinded and randomized controlled trial. Hum Reprod 2013;28(2):306–14.; Huszar G., Vigue L., Morshedi M. Sperm creatine phosphokinase M-isoform ratios and fertilizing potential of men: a blinded study of 84 couples treated with in vitro fertilization. Fertil Steril 1992;57(4):882–8.; Benchaib M., Braun V., Lornage J. et al. Sperm DNA fragmentation decreases the pregnancy rate in an assisted reproductive technique. Hum Reprod 2003;18(5):1023–8.; Virro M.R., Larson-Cook K.L., Evenson D.P. Sperm chromatin structure assay(SCSA) parameters are related to fertilization, blastocyst development, and ongoing pregnancy in in vitro fertilization and intracytoplasmic sperm injection cycles. Fertil Steril 2004;81(5):1289–95.; Seli E., Sakkas D. Spermatozoal nuclear determinants of reproductive outcome: implications for ART. Hum Reprod Update 2005;11(4):337–49.; Zini A., Borman J.M., Belzile E., Ciampi A. Sperm DNA damage is associated with an increased risk of pregnancy loss after IVF and ICSI: Systematic review and meta-analysis. Hum Reprod 2008;23(12):2663–8.; Allen J.W., Dix D.J., Collins B.W. et al. Hsp70-2 is part of the synaptonemal complex in mouse and hamster spermatocytes. Chromosoma 1996;104(6):414–21.; Dix D.J., Allen J.W., Collins B.W. et al. Targeted gene disruption of Hsp70–2 results in failed meiosis, germ cell apoptosis, and male infertility. Proc Natl Acad Sci USA 1996;93(8):3264–8.; Eddy E.M. Role of heat shock protein Hsp70–2 in spermatogenesis. Rev Reprod 1999;4(1):23–30.; Parmegiani L., Cognigni G.E., Filicori M. Sperm selection: effect on sperm DNA quality. Adv Exp Med Biol 2014;791:151–72.; Worrilow K.C., Eid S., Matthews J. et al. Multi-site clinical trial evaluating PICSI, a method for selection of hyaluronan bound sperm (HBS) for use in ICSI: improved clinical outcomes. Hum Reprod 2010;25(Suppl 1):i7.; Parmegiani L., Cognigni G.E., Ciampaglia W. et al. Efficiency of hyaluronic acid(HA) sperm selection. J Assist Reprod Genet 2010;27(1):13–6.; Nasr-Esfahani M.H., Razavi S., Vahdati A.A. et al. Evaluation of sperm selection procedure based on hyaluronic acid binding ability on ICSI outcome. J Assist Reprod Genet 2008;25(5):197–203.; Van Den Bergh M., Fahy-Deshe M., Hohl M.K. Pronuclear zygote score following intracytoplasmic injection of hyaluronan-bound spermatozoa: a prospective randomized study. Reprod Biomed Online 2009;19(6): 796–801.; Sanchez M., Aran B., Blanco J. et al. Preliminary clinical and FISH results on hyaluronic acid sperm selection to improve ICSI. Hum Reprod 2005;20(Suppl 1):i200.; Parmegiani L., Cognigni G.E., Filicori M. Risks in injecting hyaluronic acid non-bound spermatozoa. Reprod Biomed Online 2010;20(3):437–8.; https://agx.abvpress.ru/jour/article/view/160
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9Academic Journal
Συγγραφείς: ЗОБОВА АНАСТАСИЯ ВАЛЕРЬЕВНА, ДУДАРОВА А.Х., САХАРОВА Г.К., СМОЛЬНИКОВА В.Ю., МАКАРОВА Н.П.
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10Academic Journal
Πηγή: Андрология и генитальная хирургия.
Θεματικοί όροι: 0301 basic medicine, 03 medical and health sciences, ЭКСТРАКОРПОРАЛЬНОЕ ОПЛОДОТВОРЕНИЕ,IN VITRO FERTILIZATION,МУЖСКОЕ БЕСПЛОДИЕ,MALE INFERTILITY,ГИАЛУРОНОВАЯ КИСЛОТА,HYALURONIC ACID,СЕЛЕКЦИЯ СПЕРМАТОЗОИДОВ,SPERM SELECTION,ИНТРАЦИТОПЛАЗМАТИЧЕСКАЯ ИНЪЕКЦИЯ СПЕРМАТОЗОИДА,INTRACYTOPLASMIC SPERM INJECTION,ФИЗИОЛОГИЧЕСКАЯ ИНТРАЦИТОПЛАЗМАТИЧЕСКАЯ ИНЪЕКЦИЯ СПЕРМАТОЗОИДА,PHYSIOLOGICAL INTRACYTOPLASMIC SPERM INJECTION,ВСПОМОГАТЕЛЬНЫЕ РЕПРОДУКТИВНЫЕ ТЕХНОЛОГИИ,ASSISTED REPRODUCTIVE TECHNOLOGIES
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11Academic Journal
Συγγραφείς: Ковалев, В.Ю., Шишкин, А.Г.
Θεματικοί όροι: интрацитоплазматическая инъекция сперматозоида, семантическая сегментация, сверточные нейронные сети
Relation: 46;4; Dspace\SGAU\20230602\104073
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12Academic Journal
Συγγραφείς: I. I. Vityazeva, Ирина Ивановна Витязева
Πηγή: Andrology and Genital Surgery; Том 15, № 2 (2014); 6-22 ; Андрология и генитальная хирургия; Том 15, № 2 (2014); 6-22 ; 2412-8902 ; 2070-9781 ; 10.17650/2070-9781-2014-2
Θεματικοί όροι: микрохирургическая техника извлечения сперматозоидов, in vitro fertilization, intracytoplasmatic sperm injection, obstructive and nonobstructive azoospermia, microdissection testicular sperm extraction, sperm retrieval rate, AZF-deletions, экстракорпоральное оплодотворение, интрацитоплазматическая инъекция сперматозоида в ооцит, обструктивная и необструктивная азооспермия
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Relation: https://agx.abvpress.ru/jour/article/view/90/84; Willott G.M. Frequency of azoospermia. Forensic Sci Int 1982;20(1):9–10.; Jarow J.P., Espeland M.A., Lipshultz L.I. Evaluation of the azoospermic patients. J Urol 1989;142(1):62–5.; Черных В.Б. Ген муковисцидоза и нарушение фертильности у мужчин. Андрол и генит хир 2010; (4):23–31.; Matsumiya K., Namiki M., Takahara S. et al. Clinical study of azoospermia. Int J Androl 1994;17(3):140–2.; Raman J.D., Schlegel P. Testicular sperm extraction with intracytoplasmic sperm injection is successful for the treatment of nonobstructive azoospermia associated with cryptorchidism. J Urol 2003;170(4 Pt 1):1287–90.; Silber S.J., Rodriguez-Rigau L.J. Quantitative analysis of testicle biopsy: determination of partial obstruction and prediction of sperm count after surgery for obstruction. Fertil Steril 1981;36(4):480–5.; Silber S., Nagy Z., Devroey P. et al. Distribution of spermatogenesis in the testicles of azoospermic men: the presence or abscence of spermatids in the testes of men with germinal failure. Hum Reprod 1997;12(11):2422–8.; Palermo G.D., Joris K., Devroey P., Van Steirteghem A.C. Pregnancies after intracytoplasmic injection of single spermatozoon into an oocyte. Lancet 1992;340(8810):17–8.; Van Steirteghem A.C., Nagy Z., Joris H. et al. Higher fertilization and implantation rates after intracytoplasmic sperm injection. Hum Reprod 1993;8(7):1061–6.; Temple-Smith P.D., Southwick G.J., Yates C.A. et al. Human pregnancy by in vitro fertilization (IVF) using sperm aspirated from the epididymis. J In Vitro Fert Embryo Transf 1985;2(3):119–22.; Craft I., Benett V., Nicholson N. Fertilising ability of testicular spermatozoa (Letter). Lancet 1993;342(8875):864.; Schoysman R., Vanderzwalmen P., Nijs M. et al. Pregnancy after fertilisation with human testicular spermatozoa. Lancet 1993;342(8881):1237.; Devroey P., Liu J., Nagy Z. et al. Normal fertilization of human oocytes alter testicular sperm extraction and intracytoplasmic sperm injection. Fertil Steril 1994;62(3):639–41.; Devroey P., Liu J., Nagy Z. et al. Pregnancies after testicular sperm extraction and intracytoplasmic sperm injection in nonobstructive azoospermia. Hum Reprod 1995;10(6):1457–60.; Tournaye H., Camus M., Goosens A. et al. Recent concepts in the management of infertility because of non-obstructive azoospermia. Hum Reprod 1995;10(Suppl 1):115–9.; Meniru G.I., Gorgy A., Podsiadly B.T., Craft I.L. Results of percutaneous epididymal sperm aspiration and intracytoplasmic sperm injection in two major groups of patients with obstructive azoospermia. Hum Reprod 1997;12(11):2443–6.; Friedler S., Raziel A., Strassburger D. et al. Testicular sperm retrieval by percutaneous fine needle sperm aspiration compared with testicular sperm extraction by open biopsy in men with non-obstructive azoospermia. Hum Reprod 1997;12(7):1488–93.; Rosenlund B., Kvist U., Plöen L. et al. A comparison between open and percutaneous needle biopsies in men with azoospermia. Hum Reprod 1998;13(5):1266–71.; Schlegel P.N. Testicular sperm extraction: microdissection improves sperm yield with minimal tissue excision. Hum Reprod 1999;14(1):131–5.; Silber S.J. Microsurgical TESE and the distribution of spermatogenesis in nonobstructive azoospermia. Hum Reprod 2000;15(11):2278–84.; Schlegel P.N., Su L.M. Physiological consequences of testicular sperm extraction. Hum Reprod 1997;12(8):1688–92.; Tournaye H., Camus M., Vandervorst M. et al. Surgical sperm retrieval for intracytoplasmic sperm injection. Int J Androl 1997;20(Suppl 3):69–73.; Gil-Salom M., Romero J., Minguez Y. et al. Testicular sperm extraction and intracytoplasmic sperm injection: A chance of fertility in nonobstructive azoospermia. J Urol 1998;160(6 Pt 1):2063–7.; Tash J.A., Schlegel P.N. Histologic effects of testicular sperm extraction on the testicle in men with nonobstructive azoospermia. Urology 2001;57(2):334–7.; Ezeh U.I., Moore H.D.M., Cooke I.D. A prospective study of multiple needle biopsies versus a single open biopsy for testicular sperm extraction in en with non-obstructive azoospermia. Hum Reprod 1998;13(11):3075–80.; Van Peperstraten A., Proctor M.L., Johnson N.P., Philipson G. Techniques for surgical retrieval of sperm prior to ICSI for azoospermia. Cochrane Database Syst Rev 2006;(3):CD002807.; Foresta C., Garolla A., Betella A. et al. Doppler ultrasound of the testis in azoospermic subjects as a parameter of testicular function. Hum Reprod 1998;13(11):3090–3.; Har-Toov J., Eytan O., Hauser R. et al. A new power Doppler ultrasound guiding technique for improved testicular sperm extraction. Fertil Steril 2004;81(2):430–4.; Jezek D., Knuth U.A., Schulze W. Successful testicular sperm extraction (TESE) in spite of high serum follicle stimulating hormone and azoospermia: correlation between testicular morphology, TESE results, semen analysis and serum hormone values in 103 infertile men. Hum Reprod 1998;13(5):1230–4.; Levin H.S. Testicular biopsy in the study of male infertility : its current usefulness, histologic techniques, and prospects for the future. Hum Pathol 1979;10(5):569–84.; Tournaye H., Verheyen G., Nagy P. et al. Are there any predictive factors for successful testicular sperm recovery in azoospermic patients? Hum Reprod 1997;12(1):80–6.; Krausz C., Quinatana-Murci L., McElreavey K. Prognostic value of Y deletion analysis: What is the clinical prognostic value of Y chromosome microdeletion analysis? Hum Reprod 2000;15(7):1431–4.; Tiepolo L., Zuffardi O. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum Genet 1976;34(2):119–24.; Vogt P.H., Edelmann A., Kirsch S. et al. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum Mol Genet 1996;5(7):933–43.; Черных В.Б. Микроделеционный анализ AZF-локуса в рамках комплексного клинико-генетического обследования мужчин с азооспермией и олигоспермией. Автореф. дис. … канд. vед. наук. М., 2002.; Fu L., Ding X., Shen M. et al. [Screening and clinical phenotype analysis of microdeletions of azoospermia factor region on Y chromosome in 1011 infertile men]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2012;29(2):184–7.; Brandell R.A., Mielnik A., Liotta D. et al. AZFb deletions predict the absence of spermatozoa with testicular sperm extraction: preliminary report of a prognostic genetic test. Hum Reprod 1998;13(10):2812–5.; Foresta C., Moro E., Ferlin A. Prognostic value of Y deletion analysis. The role of current methods. Hum Reprod 2001;16(8):1543–7.; Sadeghi-Nejad H., Farrokhi F. Genetics of azoospermia: current knowledge, clinical implications, and future directions. Part II: Y chromosome microdeletions. J Urol 2007;4(4):192–206.; Schoor R.A., Elhanbly S., Niederberger C.S., Ross L.S. The role of testicular biopsy in the modern management of male infertility. J Urol 2002;167(1):197–200.; McLachlan R.I., Rajpert-De Meyts E., Hoei-Hansen C.E. et al. Histological evaluation of the human testis – approaches to optimizing the clinical value of the assessment: mini review. Hum Reprod 2007;22(1):2–16.; Андрология. Мужское здоровье и дисфункция репродуктивной системы. Под ред. Э. Нишлага, Г.М. Бере. М.: ООО «Медицинское информационное агентство», 2005. С. 185–7.; Efficacy and safety of highly purified urinary follicle-stimulating hormone with human chorionic gonadotropin for treating men with isolated hypogonadotropic hypogonadism. European Metrodin HP Study Group. Fertil Steril 1998;70(2):256–62.; Büchter D., Behre H.M., Kliesch S., Nieschlag E. Pulsatile GnRH or human chorionic gonadotropin / human menopausal gonadotropin as effective treatment for men with hypogonadotropic hypogonadism: a review of 42 cases. Eur J Endocrinol 1998;139(3):298–303.; Fahmy I., Kamal A., Shamloul R. et al. ICSI using testicular sperm in male hypogonadotrophic hypogonadism unresponsive to gonadotrophin therapy. Hum Reprod 2004;19(7):1558–61.; Akarsu C., Caglar G., Vicdan K. et al. Pregnancies achieved by testicular sperm recovery in male hypogonadotrophic hypogonadism with persistent azoospermia. Reprod Biomed Online 2009;18(4):455–9.; Tsujimura A. Microdissection testicular sperm extraction: prediction, outcome, and complications. Int J Urol 2007;14(10):883–9.; Hibi H., Ohori T., Yamada Y. et al. Probability of sperm recovery in nonobstructive azoospermic patients presenting with testes volume less than 10 ml/FSH level exceeding 20 mIU/ml. Arch Androl 2005;51(3):225–31.; Ramasamy R., Lin K., Gosden L.V. et al. High serum FSH levels in men with nonobstructive azoospermia does not affect success of microdissection testicular sperm extraction. Fertil Steril 2009;92(2):590–3.; Muttukrishna S., Yussoff H., Naidu M. et al. Serum anti-Müllerian hormone and inhibin B in disorders of spermatogenesis. Fertil Steril 2007;88(2):516–8.; Mostafa T., Amer M.K., Abdel-Malak G. et al. Seminal plasma anti-Müllerian hormone level correlates with semen parameters but does not predict success of testicular sperm extraction (TESE). Asian J Androl 2007;9(2):265–70.; Ballescá J.L., Balasch J., Calafell J.M. et al. Serum inhibin B determination is predictive of successful testicular sperm extraction in men with non-obstructive azoospermia. Hum Reprod 2000;15(8): 1734–8.; Von Eckardstein S., Simoni M., Bergmann M. et al. Serum inhibin B in combination with serum follicle-stimulating hormone (FSH) is a more sensitive marker than serum FSH alone for impaired spermatogenesis in men, but cannot predict the presence of sperm in testicular tissue samples. J Clin Endocrinol Metab 1999;84(7):2496–501.; Tunc L., Kirac M., Gurocak S. et al. Can serum Inhibin B and FSH levels, testicular histology and volume predict the outcome of testicular sperm extraction in patients with non-obstructive azoospermia? Int Urol Nephrol 2006;38(3–4):629–35.; Nagata Y., Fujita K., Banzai J. et al. Seminal plasma inhibin-B level is a useful predictor of the success of conventional testicular sperm extraction in patients with non-obstructive azoospermia. J Obstet Gynaecol Res 2005;31(5):384–8.; Duvilla E., Lejeune H., Trombert-Paviot B. et al. Significance of inhibin B and anti-Müllerian hormone in seminal plasma: a preliminary study. Fertil Steril 2008;89(2):444–8.; Tsujimura A., Matsumiya K., Miyagawa Y. et al. Prediction of successful outcome of microdissection testicular sperm extraction in men with idiopathic nonobstructive azoospermia. J Urol 2004;172(5 Pt 1):1944–7.; Rodrigo L., Rubio C., Mateu E. et al. Analysis of chromosomal abnormalities in testicular and epididymal spermatozoa from azoospermic ICSI patients by fluorescence insitu hybridization. Hum Reprod 2004;19(1):118–23.; Bonaparte E., Moretti M., Colpi G.M. et al. ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic men. Hum Reprod 2010;25(6):1398–403.; Ando M., Yamaguchi K., Chiba K. et al. Expression of VASA mRNA in testis as a significant predictor of sperm recovery by microdissection testicular sperm extraction in patient with nonobstructive azoospermia. J Androl 2012;33(4):711–6.; Castrillon D.H., Quade B.J., Wang T.Y. et al. The human VASA gene is specifically expressed in the germ cell lineage. Proc Natl Acad Sci USA 2000;97(17):9585–90.; Nayernia K., Adham I.M., Burkhardt-Göttges E. et al. Asthenozoospermia in mice with targeted deletion of the sperm mitochondrion-associated cysteine-rich protein (Smcp) gene. Mol Cell Biol 2002;22(9):3046–52.; Zalata A., El-Samanoudy A.Z., Shaalan D. et al. Seminal clusterin gene expression associated with seminal variables in fertile and infertile men. J Urol 2012;188(4):1260–4.; Schlegel P.N., Tanrikut A., Li P.S. Microdissection testicular sperm extraction (TESE) in non-obstructive azoospermia. Fertil Steril 2006;86:S519.; Okada H., Dobashi M., Yamazaki T. et al. Conventional versus microdissection testicular sperm extraction for non obstructive azoospermia. J Urol 2002;168:1063–7.; Amer M., Ateyah A., Hany R., Zohdy W. Prospective comparative study between microsurgical and conventional sperm extraction in non-obstructive azoospermia: follow-up by serial ultrasound examinations. Hum Reprod 2000;15(3):653–6.; Ramasamy R., Yagan N., Schlegel P.N. Structural and functional changes to the testis after conventional versus microdissection testicular sperm extraction. Urology 2005;65(6):1190–4.; Mulhall J.P., Ghaly S.W., Aviv N., Ahmed A. The utility of optical loupe magnification for testis sperm extraction in men with nonobstructive azoospermia. J Androl 2005;26(2):178–81.; Tsujimura A., Matsumiya K., Miyagawa Y. et al. Conventional multiple or microdissection testicular sperm extraction: a comparative study. Hum Reprod 2002;17(11):2924–29.; Okubo K., Ogura K., Ichioka K. et al. Testicular sperm extraction for non-obstructive azoospermia: results with conventional and microsurgical techniques. Hinyokika Kiyo 2002;48(5):275–80.; Donoso P., Tournaye H., Devroey P. Which is the best sperm retrieval technique for nonobstructive azoospermia? A systematic review. Hum Reprod Update 2007;13(6):539–49.; Tsujimura A., Miyagawa Y., Takao T. et al. Salvage microdissection testicular sperm extraction after failed conventional testicular sperm extraction in patients with nonobstructive azoospermia. J Urol 2006;175(4):1446–9.; Ramasamy R., Schlegel P.N. Microdissection testicular sperm extraction: effect of prior biopsy on success of sperm retrieval. J Urol 2007;177(4):1447–9.; Ostad M., Liotta D., Ye Z., Schlegel P.N. Testicular sperm extraction for nonobstructive azoospermia: results of a multibiopsy approach with optimized tissue dispersion. Urology 1998;52(4):692–6.; Schlegel P.N., Palermo G.D., Goldstein M. et al. Testicular sperm extraction with intracytoplasmic sperm injection for nonobstructive azoospermia. Urology 1997;49(3):435–40.; Ramasamy R., Fisher E.S., Ricci J.A. et al. Duration of microdissection testicular sperm extraction procedures: relationship to sperm retrieval success. J Urol 2011;185(4):1394–7.; Ghalayini I.F., Al-Ghazo M.A., Hani O.B. et al. Clinical comparison of conventional testicular sperm extraction and microdissection techniques for non-obstructive azoospermia. J Clin Med Res 2011;3(3):124–31.; Nicopoullos J.D., Gilling-Smith C., Almeida P.A., Ramsay J.W. The results of 154 ICSI cycles using surgically retrieved sperm from azoospermic men. Hum Reprod 2004;19(3):579–85.; Mercan R., Urman B., Alatas C. et al. Outcome of testicular sperm retrieval procedures in non-obstructive azoospermia: percutaneous aspiration versus open biopsy. Hum Reprod 2000;15(7):1548–51.; Khadra A., Abdulhadi I., Ghunain S., Kilani Z. Efficiency of percutaneous sperm aspiration as a mode of sperm collection for intracytoplasmic sperm injection in nonobstructive azoospermia. J Urol 2003;169(2):603–5.; Karacan M., Alwaeely F., Erkan S. et al. Outcome of intracytoplasmic sperm injection cycles with fresh testicular spermatozoa obtained on the day of or the day before oocyte collection and with cryopreserved testicular sperm in patients with azoospermia. Fertil Steril 2013;100(4):975–80.; Esteves S.C., Agarwal A. Reproductive outcomes, including neonatal data, following sperm injection in men with obstructive and nonobstructive azoospermia: case series and systematic review. Clinics (São Paulo) 2013;68(Suppl 1):141–50.; Gul U., Turunc T., Haydardedeoglu B. et al. Sperm retrieval and live birth rates in presumed Sertoli-cell-only syndrome in testis biopsy: a single centre experience. Andrology 2013;1(1):47–51.; Harrington T.G., Schauer D., Gilbert B.R. Percutaneous testis biopsy: an alternative to open testicular biopsy in the evaluation of the subfertile man. J Urol 1996;156(5):1647–51.; Ron-El R., Strauss S., Friedler S. et al. Serial sonography and colour flow Doppler imaging following testicular and epididymal sperm extraction. Hum Reprod 1998;13(12):3390–3.; Schill T., Bals-Pratsch M., Küpker W. et al. Clinical and endocrine follow-up of patients after testicular sperm extraction. Fertil Steril 2003;79(2):281–6.; Andersson A.M., Jorgensen N., Frydelund Larsen L. et al. Impaired Leydig cell function in infertile men: A study of 357 idiopathic infertile men and 318 proven fertile controls. J Clin Endocrinol Metab 2004;89(7):3161–7.; Everaert K., De Croo I., Kerckhert W. et al. Long term effects of micro-surgical testicular sperm extraction on androgen status on patients with non obstructive azoospermia. BMC Urol 2006;6:9.; Oliveira Filho A.B., Souza R.S., Azeredo Oliveira M.T. et al. Microdissection testicular sperm extraction causes spermatogenic alterations in the contralateral testis. Genet Mol Res 2010;9(3):1405–13.; https://agx.abvpress.ru/jour/article/view/90
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13Academic Journal
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14Academic Journal
Συγγραφείς: Нефедова, А., Пестова, Т., Русакова, М., Брюхин, Г.
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15Academic Journal
Πηγή: Андрология и генитальная хирургия.
Θεματικοί όροι: 3. Good health, ВСПОМОГАТЕЛЬНЫЕ РЕПРОДУКТИВНЫЕ ТЕХНОЛОГИИ,ASSISTED REPRODUCTIVE TECHNOLOGIES,ЭКСТРАКОРПОРАЛЬНОЕ ОПЛОДОТВОРЕНИЕ,IN VITRO FERTILIZATION,ИНТРАЦИТОПЛАЗМАТИЧЕСКАЯ ИНЪЕКЦИЯ СПЕРМАТОЗОИДА В ООЦИТ,INTRACYTOPLASMATIC SPERM INJECTION,ОБСТРУКТИВНАЯ И НЕОБСТРУКТИВНАЯ АЗООСПЕРМИЯ,OBSTRUCTIVE AND NONOBSTRUCTIVE AZOOSPERMIA,МИКРОХИРУРГИЧЕСКАЯ ТЕХНИКА ИЗВЛЕЧЕНИЯ СПЕРМАТОЗОИДОВ,SPERM RETRIEVAL RATE,ЧАСТОТА ИЗВЛЕЧЕНИЯ СПЕРМАТОЗОИДОВ,MICRODISSECTION TESTICULAR SPERM EXTRACTION,AZF-ДЕЛЕЦИИ,AZF-DELETIONS
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16Academic Journal
Πηγή: Человек. Спорт. Медицина.
Θεματικοί όροι: ЭКСТРАКОРПОРАЛЬНОЕ ОПЛОДОТВОРЕНИЕ (ЭКО),ИНТРАЦИТОПЛАЗМАТИЧЕСКАЯ ИНЪЕКЦИЯ СПЕРМАТОЗОИДА В ООЦИТ (ИКСИ),ФОЛЛИКУЛОСТИМУЛИРУЮЩИЙ ГОРМОН (ФСГ),ЧЕЛОВЕЧЕСКИЙ МЕНОПАУЗАЛЬНЫЙ ГОРМОН (ЧМГ),IN VITRO FERTILIZATION (IVF),INTRACYTOP-LASMIC SPERM INJECTION IN THE OOCYTE (ICSI),FOLLICLE-STIMULATING HORMONE (FSH),HUMAN MENOPAUSAL HORMONE (HMG), 0502 economics and business, 05 social sciences
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17Academic Journal
Πηγή: Вестник репродуктивного здоровья.
Θεματικοί όροι: 3. Good health, ЭКСТРАКОРПОРАЛЬНОЕ ОПЛОДОТВОРЕНИЕ, ВСПОМОГАТЕЛЬНЫЕ РЕПРОДУКТИВНЫЕ ТЕХНОЛОГИИ, ИНТРАЦИТОПЛАЗМАТИЧЕСКАЯ ИНЪЕКЦИЯ СПЕРМАТОЗОИДА В ООЦИТ (ИКСИ), ПРЕИМПЛАНТАЦИОННАЯ ГЕНЕТИЧЕСКАЯ ДИАГНОСТИКА (ПГД), КРИОКОНСЕРВАЦИЯ ГАМЕТ И ЭМБРИОНОВ, IN VITRO FERTILIZATION (IVF), ASSISTED REPRODUCTIVE TECHNOLOGY (ART), INTRACYTOPLASMIC SPERM INJECTION IN THE OOCYTE (ICSI), PREIMPLATATION GENETIC DIAGNOSIS (PGD)
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18Academic Journal
Συγγραφείς: Олефир Ю.В., Ефремов Е.А., Родионов М.А., Живулько А.Р., Попов Д.М., Монаков Д.М.
Πηγή: Андрология и генитальная хирургия
Θεματικοί όροι: Sperm DNA damage, male infertility, in vitro fertilization, intracytoplasmic sperm injection, intrauterine insemination, фрагментация ДНК сперматозоидов, мужское бесплодие, экстракорпоральное оплодотворение, интрацитоплазматическая инъекция сперматозоида, внутриматочная инсеминация
Διαθεσιμότητα: https://repository.rudn.ru/records/article/record/105762/
