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  1. 1
    Academic Journal

    Contributors: Авторы заявляют об отсутствии финансирования исследования.

    Source: Complex Issues of Cardiovascular Diseases; Том 14, № 3 (2025); 112-120 ; Комплексные проблемы сердечно-сосудистых заболеваний; Том 14, № 3 (2025); 112-120 ; 2587-9537 ; 2306-1278 ; undefined

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    Relation: https://www.nii-kpssz.com/jour/article/view/1692/1053; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1692/2093; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1692/2094; https://www.nii-kpssz.com/jour/article/downloadSuppFile/1692/2095; Шарипова З.У., Ахрарова Н.А., Умарова М.С. Особенности течения послеоперационного периода у детей с врожденными пороками сердца. Science and innovation. 2024; 3 (Special Issue 54): 408-413. doi:10.5281/zenodo.14185925.; Саперова Е.В., Вахлова И.В. Врожденные пороки сердца у детей: распространенность, факторы риска, смертность. Вопросы современной педиатрии. 2017; 16(2): 126-133.; Санталова Г.В., Шорохов С.Е., Стадлер Е.Р., Авраменко А.А., Горбунова А.В., Нуруллина А.В. Критические врожденные пороки сердца новорожденных. Вопросы практической педиатрии. 2019; 14(5): 78-86. doi:10.20953/1817-7646-2019-5-76-86.; Zubrzycki M., Schramm R., Costard-Jäckle A., Grohmann J., Gummert J.F., Zubrzycka M. Cardiac Development and Factors Influencing the Development of Congenital Heart Defects (CHDs): Part I. Int J Mol Sci. 2024;25(13):7117. doi:10.3390/ijms25137117.; Villavicencio-Guzmán L., Sánchez-Gómez C., Jaime-Cruz R., Ramírez-Fuentes T.C., Patiño-Morales C.C., Salazar-García M. Human Heart Morphogenesis: A New Vision Based on In Vivo Labeling and Cell Tracking. Life. 2023;13:165. doi:10.3390/life13010165.; Courtney J.A., Cnota J.F., Jones H.N. The Role of Abnormal Placentation in Congenital Heart Disease; Cause, Correlate, or Consequence? Front Physiol. 2018;9:1045. doi:10.3389/fphys.2018.01045.; Cole C.R., Yutzey K.E., Brar A.K., Goessling L.S., Van Vickle-Chavez S.J., Cunningham M.W., Eghtesady P. Congenital Heart Disease Linked to Maternal Autoimmunity against Cardiac Myosin. J Immunol. 2014;192:4074-4082. doi:10.4049/jimmunol.1301264.; Salmeri N., Seidenari A., Cavoretto P.I., Papale M., Candiani M., Farina A. Maternal prepregnancy weight as an independent risk factor for congenital heart defect: systematic review and meta-analysis stratified by subtype and severity of defect. Ultrasound Obstet Gynecol. 2024;64(3):294-307. doi:10.1002/uog.27659.; Понасенко А.В., Цепокина А.В. Посттранскрипционное регулирование в развитии врождённых пороков сердца: значение микроРНК. Комплексные проблемы сердечно-сосудистых заболеваний. 2019;8(3):85-95. doi:10.17802/2306-1278-2019-8-3-85-95.; Kelly A.C., Powell T.L., Jansson T. Placental function in maternal obesity. Clin Sci (Lond). 2020;134(8):961-984. doi:10.1042/CS20190266.; Артымук Н.В., Тачкова О.А., Шурыгин С.Н. "Порочный репродуктивный круг" ожирения: обзор литературы. Доктор.Ру. 2018; (10)154: 22-26. doi:10.31550/1727-2378-2018-154-10-22-26.; Xiao-Xia Wu, Ru-Xiu Ge, Le Huang, Fu-Ying Tian, Yi-Xuan Chen, Lin-Lin Wu, Jian-Min Niu. Maternal Obesity and the Risk of Congenital Heart Defects: the Mediation Effect of Pregestational Diabetes. Preprint 20 April 2021. doi:10.21203/rs.3.rs-430110/v1; Liang J. Progress of pregestational diabetes mellitus and congenital heart defects. Int J Pediatr. 2010;37:484-486. doi:10.3760/CMA.J.ISSN.1673-4408.2010.05.014.; Chen Z., Mao S., Guo L., Qin J., Yang L.X., Liu Y. Effect of maternal pregestational diabetes mellitus on congenital heart diseases. World J Pediatr. 2022;19:303-314. doi:10.1007/s12519-022-00582-w.; Sharifi A., Ekram K., Wali W. The spectrum of congenital heart defects in neonates of diabetic mothers. Pediomaternal Nurs J. 2023;9(2). doi:10.20473/pmnj.v9i2.39020.; Chen L., Yang T., Chen L., Wang L., Wang T., Zhao L., Ye Z., Zhang S., Luo L., Zheng Z., Qin J. Risk of congenital heart defects in offspring exposed to maternal diabetes mellitus: An updated systematic review and meta-analysis. Arch Gynecol Obstet. 2019;300:1491-1506. doi:10.1007/s00404-019-05289-4.; Ibrahim S., Gaborit B., Lenoir M., Collod-Beroud G., Stefanovic S. Maternal Pre-Existing Diabetes: A Non-Inherited Risk Factor for Congenital Cardiopathies. Int J Mol Sci. 2023;24:16258. doi:10.3390/ijms242316258.; Köse S., Sözlü S., Bölükbaşi H., Ünsal N., Gezmen-Karadağ M. Obesity is associated with folate metabolism. Int J Vitam Nutr Res. 2020;90(3-4):353-364. doi:10.1024/0300-9831/a000602.; Gu Q., Li Y., Cui Z.L., Luo X.P. Homocysteine, folate, vitamin B12 and B6 in mothers of children with neural tube defects in Xinjiang, China. Acta Paediatr. 2012;101:e486-e490. doi:10.1111/j.1651-2227.2012.02781.x.; Mitchell L.E., Long J., Garbarini J., Paluru P., Goldmuntz E. Variants of folate metabolism genes and risk of left-sided cardiac defects. Birth Defects Res A Clin Mol Teratol. 2010;88:48-53. doi:10.1002/bdra.20635.; Li F. Folic acid and birth defects. Int J Pediatr. 2019;46:640-643. doi:10.3760/CMA.J.ISSN.1673-4408.2019.09.006.; Liu H., Ou J., Chen Y., Chen Q., Luo M., Wang T., Qin J. Association of Maternal Folate Intake and Offspring MTHFD1 and MTHFD2 Genes with Congenital Heart Disease. Nutrients. 2023;15:3502. doi:10.3390/nu15163502.; Yelbuz T.M, Waldo K.L, Kumiski D.H, Stadt H.A., Wolfe R.R., Leatherbury L., Kirby M.L. Shortened outflow tract leads to altered cardiac looping after neural crest ablation. Circulation. 2002;106:504-510. doi:10.1161/01.CIR.0000023044.44974.8A.; Szymanski P., Klisiewicz A., Lubiszewska B., Lipczyńska M., Konka M., Kuśmierczyk M., Hoffman P. Functional anatomy of tricuspid regurgitation in patients with systemic right ventricles. J Am Soc Echocardiogr. 2010;23:504-510. doi:10.1016/j.echo.2010.02.006.; Liu S., Joseph K., Lisonkova S., Rouleau J., Van Den Hof M., Sauve R., Kramer M. Association Between Maternal Chronic Conditions and Congenital Heart Defects: A Population-Based Cohort Study. Circulation. 2013; 128: 583–589. doi:10.1161/CIRCULATIONAHA.112.001054.; Kilkenny K., Frishman W. Preeclampsia's Cardiovascular Aftermath: A Comprehensive Review of Consequences for Mother and Offspring. Cardiology in review. 2024. doi:10.1097/CRD.0000000000000639.; Тезиков Ю.В., Липатов И.С., Гогель Л.Ю., Азаматов А.Р., Эрметов В.К. Перинатальный подход к клинической классификации хронической плацентарной недостаточности: стандартизация диагностики и акушерской тактики. Наука и инновации в медицине. 2019; 4 (1): 8–15. doi:10.35693/2500-1388-2019-4-1-8-15.; Brodwall K., Leirgul E., Greve G., Vollset S., Holmstrøm H., Tell G., Øyen N. Possible Common Aetiology behind Maternal Preeclampsia and Congenital Heart Defects in the Child: a Cardiovascular Diseases in Norway Project Study. Paediatric and perinatal epidemiology. 2016; 30 (1): 76–85. doi:10.1111/ppe.12252.; Liu J., Zhao G., Xie J., Wu S., Li B., Yao J. There is a Strong Association between Early Preeclampsia and Congenital Heart Defects: A Large Population-Based, Retrospective Study. Gynecologic and Obstetric Investigation. 2020; 86: 40–47. doi:10.1159/000506804.; Emanuel J., Iannuzzelli A., Venkataraman V. Investigating the Link Between Preeclampsia/Eclampsia in Mothers and Cardiovascular Risk Among Their Neurodivergent Children. Research Posters. 2024. doi:10.31986/issn.2689-0690_rdw.stratford_research_day.141_2024.; Lin S., Herdt-Losavio M., Gensburg L., Marshall E., Druschel C. Maternal asthma, asthma medication use, and the risk of congenital heart defects. Birth Defects Res A Clin Mol Teratol. 2009;85:161-168. doi:10.1002/bdra.20523.; Szabó A, Mayor R. Mechanisms of neural crest migration. Annu Rev Genet. 2018;52:43-63. doi:10.1146/annurev-genet-120417-031559.; Чернова Т.М., Тимченко В.Н., Павлова Е.Б., Баракина Е.В. Врожденные краснуха и корь в периоде глобальной ликвидации. Педиатрия. 2019;98(3):172-179.; George S., Viswanathan R., Sapkal G. Molecular aspects of the teratogenesis of rubella virus. Biol Res. 2019;52:47. doi:10.1186/s40659-019-0254-3.; Bilz N., Willscher E., Binder H., Böhnke J., Stanifer M.L., Hübner D., Boulant S., Liebert U.G., Claus C. Teratogenic Rubella Virus Alters the Endodermal Differentiation Capacity of Human Induced Pluripotent Stem Cells. Cells. 2019;8:870. doi:10.3390/cells8080870.; Priyanka P., Vyas V., Deora S., Nag V.L., Singh K. Epidemiology, etiology and clinical associations of congenital heart disease identified during congenital rubella syndrome surveillance. J Trop Pediatr. 2022;68(6). doi:10.1093/tropej/fmac089.; Yazigi A., De Pecoulas A., Vauloup-Fellous C., Grangeot-Keros L., Ayoubi J.M., Picone O. Fetal and neonatal abnormalities due to congenital rubella syndrome: a review of literature. J Matern Fetal Neonatal Med. 2017;30(3):274-278. doi:10.3109/14767058.2016.1169526.; Osman M., Zakaria M., Alnofal M., Hamdoun S.A., Alissa M.S. Congenital rubella syndrome: a case report. Int J Contemp Pediatr. 2020;7(4):1-3. doi:10.18203/2349-3291.ijcp20204052.; Kuciene .R, Dulskienė V. Selected environmental risk factors and congenital heart defects. Medicina (Kaunas). 2008;44(11):827-832. doi:10.3390/medicina44110104.; Shalen E.F, McGrath L.B, Bhamidipati C.M, Garcia I.C., Ramsey K., Broberg C.S., Khan A.M. Substance Use Disorders Are Prevalent in Adults With Congenital Heart Disease and Are Associated With Increased Healthcare Use. Am J Cardiol. 2023;192:24-30. doi:10.1016/j.amjcard.2023.01.012.; Cipollone D., Amati F., Carsetti R., Placidi S., Biancolella M., D'Amati G., Novelli G., Siracusa G., Marino B. A multiple retinoic acid antagonist induces conotruncal anomalies, including transposition of the great arteries, in mice. Cardiovasc Pathol. 2006;15:194-202. doi:10.1016/j.carpath.2006.04.001.; Liu Y., Xiao A. Epigenetic regulation in neural crest development. Birth Defects Res A Clin Mol Teratol. 2011;91:788-796. doi:10.1002/bdra.20783.; Taylor I.M, Wiley M.J, Agur A. Retinoic acid-induced heart malformations in the hamster. Teratology. 1980;21:193-197. doi:10.1002/tera.1420210208.; Kuehl K.S, Loffredo C.A. Genetic and environmental influences on malformations of the cardiac outflow tract. Expert Rev Cardiovasc Ther. 2005;3:1125-1130. doi:10.1586/14779072.3.6.1125.; Loffredo C.A, Silbergeld E.K, Ferencz C., Zhang J. Association of transposition of the great arteries in infants with maternal exposures to herbicides and rodenticides. Am J Epidemiol. 2001;153:529-536. doi:10.1093/aje/153.6.529.; Шабалдин А.В., Цепокина А.В., Шмулевич С.А., Табакаев М.В., Шабалдина Е.В. Влияние социальных, медицинских и экологических факторов на формирование спорадических врожденных пороков сердца. Российский вестник перинатологии и педиатрии. 2018; 63(1): 14–21. doi:10.21508/1027-4065-2018-63-1-14-21.; Yang B., Qu Y., Guo Y., Markevych I., Heinrich J., Bloom M.S., Bai Z., Knibbs L.C., Li S., Chen G. et al. Maternal exposure to ambient air pollution and congenital heart defects in China. Environ Int. 2021;153:106548. doi:10.1016/j.envint.2021.106548; Michel S., Atmakuri A., Von Ehrenstein O. Prenatal exposure to ambient air pollutants and congenital heart defects: An umbrella review. Environ Int. 2023;178:108076. doi:10.1016/j.envint.2023.108076.; Gorini F., Chiappa E., Gargani L., Picano E. Potential Effects of Environmental Chemical Contamination in Congenital Heart Disease. Pediatr Cardiol. 2014;35:559-568. doi:10.1007/s00246-014-0870-1.; Carmichael S., Yang W., Roberts E., Kegley S.E., Padula A.M., English P.B., Lammer E.J., Shaw G.M. Residential agricultural pesticide exposures and risk of selected congenital heart defects among offspring in the San Joaquin Valley of California. Environ Res. 2014;135:133-138. doi:10.1016/j.envres.2014.08.030.; Hu C., Huang K., Fang Y., Yang X.J., Ding K., Jiang W., Hua X.G., Huang D.Y., Jiang Z.X., Zhang X.J. Maternal air pollution exposure and congenital heart defects in offspring: A systematic review and meta-analysis. Chemosphere. 2020;253:126668. doi:10.1016/j.chemosphere.2020.126668.

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    Academic Journal

    Subject Geographic: USPU

    Relation: Специальное образование. 2019. № 3 (55)

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    Academic Journal

    Source: Ukrainian Journal of Perinatology and Pediatrics; No. 3(91) (2022): Ukrainian Journal of Perinatology and Pediatrics; 54-60
    Украинский журнал Перинатология и Педиатрия; № 3(91) (2022): Ukrainian Journal of Perinatology and Pediatrics; 54-60
    Український журнал Перинатологія і Педіатрія; № 3(91) (2022): Український журнал Перинатологія і Педіатрія; 54-60

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    Academic Journal

    Source: Ukrainian Therapeutical Journal; № 3-4 (2018); 86-95
    Украинский терапевтический журнал; № 3-4 (2018); 86-95
    Український терапевтичний журнал; № 3-4 (2018); 86-95

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    Academic Journal

    Source: Actual Problems of Pediatry, Obstetrics and Gynecology; No. 1 (2008) ; Актуальные вопросы педиатрии, акушерства и гинекологии; № 1 (2008) ; Актуальні питання педіатрії, акушерства та гінекології; № 1 (2008) ; 2415-301X ; 2411-4944 ; 10.11603/24116-4944.2008.1

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    Academic Journal

    Source: Rational Pharmacotherapy in Cardiology; Vol 15, No 2 (2019); 258-264 ; Рациональная Фармакотерапия в Кардиологии; Vol 15, No 2 (2019); 258-264 ; 2225-3653 ; 1819-6446 ; 10.20996/1819-6446-2019-15-2

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    Relation: https://www.rpcardio.com/jour/article/view/1923/1812; Williams B., Mancia G., Spiering W. et al.; Authors/Task Force Members. 2018 ESC/ESH Guidelines for the management of arterial hypertension: The Task Force for the management of arterial hypertension of the European Society of Cardiology and the European Society of Hypertension: The Task Force for the management of arterial hypertension of the European Society of Cardiology and the European Society of Hypertension. J Hypertens. 2018;36(10):1953-2041. doi:10.1097/HJH.0000000000001940.; Obisesan TO., Obisesan O.A., Martins S. et al. High blood pressure, hypertension, and high pulse pressure are associated with poorer cognitive function in persons aged 60 and older: the Third National Health and Nutrition Examination Survey. J Am Geriatr Soc. 2008;56:501-9. doi:10.1111/j.15325415.2007.01592.x.; Kuo H.K., Sorond IF, Iloputaife I. et al. Effect of blood pressure on cognitive functions in elderly persons. J Gerontol A Biol Sci Med Sci. 2004;59:1191-4. doi:10.1111/j.1532-5415.2007.01592.x.; Waldstein S.R., Giggey P.P., Thayer J.F, Zonderman A.B. Nonlinear relations of blood pressure to cognitive function: the Baltimore Longitudinal Study of Aging. Hypertension. 2005;45:374-9. doi:10.1161/01.HYP.0000156744.44218.74.; Elias M.F, Wolf PA., D'Agostino R.B. et al. Untreated blood pressure level is inversely related to cognitive functioning: the Framingham Study Am J Epidemiol. 1993;138:353-64.; Launer L.J., Masaki K., Petrovitch H. et al. The association between midlife blood pressure levels and late-life cognitive function: the Honolulu-Asia Aging Study, JAMA. 1 995;274:1846-51.; Elias P.K., Elias M.F, Robbins M.A., Budge M.M. Blood pressure related cognitive decline: does age make a difference? Hypertension. 2004;44:631-6. doi:10.1161/01.HYP.0000145858.07252.99; Debette S., Seshadri S., Beiser A. et al. Midlife vascular risk factor exposure accelerates structural brain aging and cognitive decline. Neurology 2011 ;77:461-8. doi:10.1212/WNL.0b013e318227b227.; Kohler S., Baars M.A., Spauwen P. et al. Temporal evolution of cognitive changes in incident hypertension: prospective cohort study across the adult age span. Hypertension. 2014;63:245-51. doi:10.1161/hYPERTENSIONAHA.113.02096.; Парфенов В.А., Старчина Ю.А. Когнитивные нарушения у пациентов с артериальной гипертензией и их лечение. Неврология, Нейропсихиатрия, Психосоматика. 2011 ;3(1):27-33. doi:10.14412/2074-2711-2011-130.; Cui J., Yu R., Li M. et al. Intervention affects the cognitive performance of middle-aged patients with essential hypertension. Int J Clin Exp Med 2016;9(1):308-315.; Shehab A., Abdulle A. Cognitive and autonomic dysfunction measures in normal controls, white coat and borderline hypertension.). BMC Cardiovasc Disord. 2011 ;11:3. doi:10.1186/1471-2261-11-3.; Парфенов В.А., Остроумова Т.М., Остроумова О.Д., Павлеева Е.Е. Особенности клинической картины у пациентов среднего возраста с эссенциальной артериальной гипертензией. Терапевтический Архив. 2018;90(9): 1 5-26. doi:10.26442/terarkh20189091526.; Obisesan TO., Obisesan O.A., Martins S. et al. High blood pressure, hypertension, and high pulse pressure are associated with poorer cognitive function in persons aged 60 and older: the Third National Health and Nutrition Examination Survey J Am Geriatr Soc. 2008;56:501-9. doi:10.1111/j.1532-5415.2007.01592.x.; Waldstein S.R., Rice S.C., Thayer J.F. et al. Pulse pressure and pulse wave velocity are related to cognitive decline in the Baltimore Longitudinal Study of Aging. Hypertension. 2008;51:99-1 04. doi:10.1161/HYPERTENSIONAHA.107.093674.; Kilander L., Nyman H., Boberg M. et al. Hypertension is related to cognitive impairment: a 20-year follow-up of 999 men. Hypertension. 1998; 31:780-6.; Tsivgoulis G., Alexandrov A.V, Wadley V.G. et al. Association of higher diastolic blood pressure levels with cognitive impairment. Neurology 2009;73:589-95. doi:10.1212/WNL.0b013e3181b38969.; Waldstein S.R., Giggey P.P., Thayer J.F, Zonderman A.B. Nonlinear relations of blood pressure to cognitive function: the Baltimore Longitudinal Study of Aging. Hypertension. 2005;45:374-9. doi :10.1161/01.HYP.0000156744.44218.74.; White WB., Wolfson L., Wakefield D.B. et al. Average Daily Blood Pressure, not Office Blood Pressure, is Associated with Progression of Cerebrovascular Disease and Cognitive Decline in Older People. Circulation. 2011 ;1 24(21 ):231 2-9. doi:10.1161/CIRCULATIONAHA.111.037036; Conway K.S., Forbang N., Beben T et al. Relationship Between 24-Hour Ambulatory Blood Pressure and Cognitive Function in Community-Living Older Adults: The UCSD Ambulatory Blood Pressure Study. Am J Hypertens. 2015;28(12):1444-52. doi:10.1093/ajh/hpv042.; Gonzalez-Rojas C.A., Pino-Ramirez G., Partida A.G. et al. Ambulatory blood pressure and cognitive function in nondemented older adults: Findings of the maracaibo aging study. Alzheimer's & Dementia: 2010;6(4 Suppl):S477.; Conway K.S., Forbang N., Beben T. et al. Relationship Between 24-Hour Ambulatory Blood Pressure and Cognitive Function in Community-Living Older Adults: The UCSD Ambulatory Blood Pressure Study, Am J Hypertens. 2015;28(12):1444-52. doi:10.1093/ajh/hpv042.; Nagai M., HoshideS., Ishikawa J. et al. Ambulatory blood pressure as an independent determinant of brain atrophy and cognitive function in elderly hypertension. J Hypertens. 2008;26(8):1636-41. doi:10.1097/HJH.0b013e3283018333.; Okuno J., Yanag H. Cognitive impairment and nocturnal blood pressure fall in treated elderly hypertensives. Environ Health Prev Med. 2003;8(4):124-32. doi:10.1007/BF02897916.; Sierra C., Salamero M., Domenech M. et al. Circadian Blood Pressure Pattern and Cognitive Function in Middle-aged Essential Hypertensive Patients. Rev Esp Cardiol (Engl Ed). 2015;68(2):1 57-8. doi :10.1016/j.rec.2014.09.009.; O'Brien E., Parati G., Stergiou G. et al.; European Society of Hypertension Working Group on Blood Pressure Monitoring Guidelines European Society of Hypertension Position Paper on Ambulatory Blood Pressure Monitoring. Journal of Hypertension. 2013;31 (9):1 731 -68. doi:10.1097/HJH.0b013e328363e964.; Bellelli G., Pezzini A., Bianchetti A., Trabucchi M. Increased blood pressure variability may be associated with cognitive decline in hypertensive elderly subjects with no dementia. Arch Intern Med. 2002;1 62(4):483-4.; Cho N., Hoshide S., Nishizawa M. et al. Relationship Between Blood Pressure Variability and Cognitive Function in Elderly Patients With Good Blood Pressure Control. Am J Hypertens. 2018;31(3):293-8. doi :10.1093/ajh/hpx155.; Kanemary A., Kanemary K., Kuwajima I. 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    Academic Journal

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    Relation: Мануша Ю. І. Висвітлення спільних патогенетичних механізмів розвитку системного запалення при неалкогольній жировій хворобі печінки та ішемічній хворобі серця / Ю. І. Мануша, Ю. М. Казаков // Актуальні проблеми сучасної медицини. – 2017. – № 3 (59), Т. 17. – С. 277–281.; https://repository.pdmu.edu.ua/handle/123456789/3139

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