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    Academic Journal

    Source: Obstetrics, Gynecology and Reproduction; Vol 18, No 5 (2024); 743-753 ; Акушерство, Гинекология и Репродукция; Vol 18, No 5 (2024); 743-753 ; 2500-3194 ; 2313-7347

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    Relation: https://www.gynecology.su/jour/article/view/2196/1252; Simonsen K.A., Anderson-Berry L.N., Delair S.F. et al. Early-onset neonatal sepsis. Clin Microbiol Rev. 2014;27(1):21–47. https://doi.org/10.1128/CMR.00031-13.; Боронина Л.Г., Саматова Е.В., Пруткин М.Е. Расширение возможностей в диагностике бактериемии и сепсиса у детей многопрофильного стационара. Клиническая лабораторная диагностика. 2019;64(10):613–9. https://doi.org/10.18821/0869-2084-2019-64-10-613-619.; Анохин В.А., Халиуллина С.В., Назарова О.А., Хаертынов Х.С. Случай раннего неонатального сепсиса, обусловленного Corynebacterium amycolatum. Практическая медицина. 2012;7(62):178–80.; Карпова А.Л., Ковалева М.А., Карпов Н.Ю. и др. Врожденная инфекция, вызванная вирусом SARS-CoV-2: обзор литературы и первое клиническое наблюдение у недоношенного новорожденного ребенка в России. Педиатрия имени Г.Н. Сперанского. 2022;101(1):209–14. https://doi.org/10.24110/0031-403X-2022-101-1-209-214.; Карпова А.Л., Мостовой А.В., Мартиросян С.В. и др. Ранний неонатальный сепсис, вызванный Haemophilus influenzae. Акушерство, Гинекология и Репродукция. 2023;17(3):366–75. https://doi.org/10.17749/2313-7347/ob.gyn.rep.2023.415.; Diekema D.J., Pfaller M.A., Jones R.N. et al. Trends in antimicrobial susceptibility of bacterial pathogens isolated from patients with bloodstream infections in the USA, Canada and Latin America. SENTRY Participants Group. Int J Antimicrob Agents. 2000;13(4):257–71. https://doi.org/10.1128/spectrum.01462-21.; Fluit A.C., Jones M.E., Schmitz F.J. et al. Antimicrobial susceptibility and frequency of occurrence of clinical blood isolates in Europe from the SENTRY antimicrobial surveillance program 1997 and 1998. Clin Infect Dis. 2000;30(3):454–60. https://doi.org/10.1086/313710.; Barry R., Houlihan E., Knowles S.J. et al. Antenatal pyelonephritis: a three-year retrospective cohort study of two Irish maternity centres. Eur J Clin Microbiol Infect Dis. 2023;42(7):827–33. https://doi.org/10.1007/s10096-023-04609-6.; Unhanand M., Mustafa M.M., McCracken G.H., Nelson J.D. Gram-negative enteric bacillary meningitis: a twenty-one-year experience. J Pediatr. 1993;122(1):15–21. https://doi.org/10.1016/S0022-3476(05)83480-8.; Sikias P., Biran V., Foix-L'Hélias L. et al.; EOS study group. Early-onset neonatal sepsis in the Paris area: a population-based surveillance study from 2019 to 2021. Arch Dis Child Fetal Neonatal Ed. 2023;108(2):114–20. https://doi.org/10.1136/archdischild-2022-324080.; Nabi S.N., Basak A.K., Kamruzzaman M. et al. Performance of haematological parameters in early diagnosis of clinically suspected neonatal sepsis. Mymensingh Med J. 2019;28(1):193–9.; Shabaan A.E., Elbaz L.M., El-Emshaty W.M., Shouman B. Role of serum (1,3)-β-d-glucan assay in early diagnosis of invasive fungal infections in a neonatal intensive care unit. J Pediatr (Rio J). 2018;94(5):559–65. https://doi.org/10.1016/j.jped.2017.07.020.; Boulos A., Rand K., Johnson J.A. et al. Neonatal sepsis in Haiti. J Trop Pediatr. 2017;63(1):70–3. https://doi.org/10.1093/tropej/fmw077.; Hervás J.A., Ciria L., Henales V. et al. Nonsurgical management of neonatal multiple brain abscesses due to Proteus mirabilis. Helv Paediatr Acta. 1987;42(5–6):451–6.; Casadevall I., Betremieux P., Donnio P.Y. et al. Neonatal Proteus mirabilis septicemia and cerebral abscess. Value of the assay of antibiotics in the puncture fluid. Pediatrie. 1989;44(2):97–101. (In French).; Omoruyi E.A., Evangelista M. Proteus mirabilis septicemia and meningitis in a neonate. J Med Cases. 2014;5(4):245–7. https://doi.org/10.14740/jmc1290w.; Darby C.P., Conner E., Kyong C.U. Proteus mirabilis brain abscess in a neonate. Dev Med Child Neurol. 1978;20(3):366–8. https://doi.org/10.1111/j.1469-8749.1978.tb15226.x.; Okubo T., Shirane R., Mashiyama S. Proteus mirabilis brain abscess in a neonate. No Shinkei Geka. 1984;12(3 Suppl):395–400. (In Japanese).; Carre M., Sarlangue J., Baronnet R. et al. Cerebral abscess caused by Proteus mirabilis in the neonatal period. Arch Fr Pediatr. 1987;44(10):871–4. (In French).; Chung M.H., Kim G., Han A., Lee L. Case report of neonatal Proteus mirabilis meningitis and brain abscess with negative initial image finding: Consideration of serial imaging studies. Neonatal Med. 2017;24(4):187–91. https://doi.org/10.5385/nm.2017.24.4.187.; Lizardo-Barahona J.R., Nieto-Zermeño J., Bracho-Blanchet E. Adrenal abscess in the newborn: a case report and review of the literature. Bol Med Hosp Infant Mex. 1990;47(6):401–4. (In Spanish).; Hashmi M.A., Lodhi M.A., Toor K.M. et al. Emerging antimicrobial resistance in neonatal sepsis. J Coll Physicians Surg Pak. 2020;30(12):1312–5. https://doi.org/10.29271/jcpsp.2020.12.1312.; Ballot D.E., Bandini R., Nana T. et al. A review of-multidrug-resistant Enterobacteriaceae in a neonatal unit in Johannesburg, South Africa. BMC Pediatr. 2019;19(1):320. https://doi.org/10.1186/s12887-019-1709-y.; Aku F.Y., Akweongo P., Nyarko K. et al. Bacteriological profile and antibiotic susceptibility pattern of common isolates of neonatal sepsis, Ho Municipality, Ghana-2016. Matern Health Neonatol Perinatol. 2018;4:2. https://doi.org/10.1186/s40748-017-0071-z.; Jain S., Gaind R., Kothari C. et al. VEB-1 extended-spectrum β-lactamase-producing multidrug-resistant Proteus mirabilis sepsis outbreak in a neonatal intensive care unit in India: clinical and diagnostic implications. JMM Case Rep. 2016;3(4):e005056. https://doi.org/10.1099/jmmcr.0.005056.; Ahmad A., Sarwar N., Aslam R. et al. Pattern of clinical drug resistance and occurrence of Gram negative bacterial neonatal sepsis at a tertiary care hospital. Pak J Pharm Sci. 2021;34(5(Supplementary)):1873–8.; Ullah O., Khan A., Ambreen A. et al. Antibiotic sensitivity pattern of bacterial isolates of neonatal septicemia in Peshawar, Pakistan. Arch Iran Med. 2016;19(12):866–9.; Silverman W.A., Andersen D.H. A controlled clinical trial of effects of water mist on obstructive respiratory signs, death rate and necropsy findings among premature infants. Pediatrics. 1956;17(1):1–10.; Cetinkaya M., Köksal N., Özkan H. A new scoring system for evaluation of multiple organ dysfunction syndrome in premature infants. Am J Crit Care. 2012;21(5):328–37. https://doi.org/10.4037/ajcc2012312.; Мостовой А.В., Карпова А.Л. Искусственная вентиляция легких у новорожденных: физиологические особенности газообмена и механики дыхания как основа для управления параметрами вентиляции. Детские болезни сердца и сосудов. 2016;13(2):79–87.; Карпова А.Л., Мостовой А.В., Прутко Е.Е. и др. Интерлейкин-6 как индикатор тяжести полиорганной недостаточности у недоношенных детей с массой тела менее 1500 г: ретроспективное когортное исследование. Педиатрия имени Г.Н. Сперанского. 2023;102(1):54–63. https://doi.org/10.24110/0031-403X-2023-102-1-54-63.; Eichberger J., Resch E., Resch B. Diagnosis of neonatal sepsis: the role of inflammatory markers. Front Pediatr. 2022;10:840288. https://doi.org/10.3389/fped.2022.840288.; Qiu X., Zhang L., Tong Y. et al. Interleukin-6 for early diagnosis of neonatal sepsis with premature rupture of the membranes: A meta-analysis. Medicine (Baltimore). 2018;97(47):e13146. https://doi.org/10.1097/MD.0000000000013146.; Бронхолегочная дисплазия. Монография. Под ред. Д.Ю. Овсянникова, Н.А. Геппе, А.Б. Малахова, Д.Н. Дегтярева. М., 2020. 175 c.; Мостовой А.В., Карпова А.Л., Попов И.В. и др. Лаваж легких сурфактантом при неонатальном синдроме аспирации мекония как жизнеспасающая респираторная стратегия: клинический случай. Акушерство, Гинекология и Репродукция. 2024;18(4):581–95. https://doi.org/10.17749/2313-7347/ob.gyn.rep.2024.533.; Berger C., Uehlinger J., Ghelfi D. et al. Comparison of C-reactive protein and white blood cell count with differential in neonates at risk for septicaemia. Eur J Pediatr. 1995;154(2):138–44. https://doi.org/10.1007/BF01991918.; Jurges E.S., Henderson D.C. Inflammatory and immunological markers in preterm infants: correlation with disease. Clin Exp Immunol. 1996;105(3):551–5. https://doi.org/10.1046/j.1365-2249.1996.d01-789.x.; Chiesa C., Fabrizio S., Assumma M. et al. Serial measurements of C-reactive protein and interleukin-6 in the immediate postnatal period: reference intervals and analysis of maternal and perinatal confounders. Clin Chem. 2001;47(6):1016–22.; Benitz W.E. Adjunct laboratory tests in the diagnosis of early-onset neonatal sepsis. Clin Perinatol. 2010;37(2):421–38. https://doi.org/10.1016/j.clp.2009.12.001.; Bancalari E., Claure N., Sosenko I.R. Bronchopulmonary dysplasia: changes in pathogenesis, epidemiology and definition. Semin Neonatol. 2003;8(1):63–71. https://doi.org/10.1016/s1084-2756(02)00192-6.; Schuchat A., Dowell S.F. Pneumonia in children in the developing world: new challenges, new solutions. Semin Pediatr Infect Dis. 2004;15(3):181–9. https://doi.org/10.1053/j.spid.2004.05.010.; Puopolo K.M., Benitz W.E., Zaoutis T.E.; COMMITTEE ON FETUS AND NEWBORN; COMMITTEE ON INFECTIOUS DISEASES. Management of neonates born at ≤ 34 6/7 weeks' gestation with suspected or proven early-onset bacterial sepsis. Pediatrics. 2018;142(6):e20182896. https://doi.org/10.1542/peds.2018-2896.; https://www.gynecology.su/jour/article/view/2196

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    Academic Journal

    Source: Сборник статей

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    Relation: Актуальные вопросы современной медицинской науки и здравоохранения: материалы VII Международной научно-практической конференции молодых учёных и студентов, Екатеринбург, 17-18 мая 2022 г.; http://elib.usma.ru/handle/usma/7355

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    Academic Journal

    Source: Zaporozhye мedical journal; Vol. 24 No. 1 (2022); 102-108 ; Запорожский медицинский журнал; Том 24 № 1 (2022); 102-108 ; Запорізький медичний журнал; Том 24 № 1 (2022); 102-108 ; 2310-1210 ; 2306-4145

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    Academic Journal

    Source: Acta Biomedica Scientifica; Том 7, № 3 (2022); 22-29 ; 2587-9596 ; 2541-9420

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    Relation: https://www.actabiomedica.ru/jour/article/view/3541/2351; Ananth CV, Chauhan SP. Epidemiology of twinning in developed countries. Semin Perinatol. 2012; 36(3): 156-161.; D’Antonio F, Odibo AO, Prefumo F, Khalil A, Buca D, Flacco ME, et al. Weight discordance and perinatal mortality in twin pregnancy: Systematic review and meta-analysis. Ultrasound Obstet Gynecol. 2018; 52(1): 11-23. doi:10.1002/uog.18966; Kulkarni AD, Jamieson DJ, Jones HW Jr, Kissin DM, Gallo MF, Macaluso M, et al. Fertility treatments and multiple births in the United States. N Engl J Med. 2013; 369(23): 2218-2225. doi:10.1056/NEJMoa1301467; D’Alton M, Breslin N. Management of multiple gestations. Int J Gynaecol Obstet. 2020; 150(1): 3-9. doi:10.1002/ijgo.13168; Hamilton ВЕ, Martin JA, Osterman MJ, Curtin SC, Matthews TJ. Births: Final data for 2014. Natl Vital Stat Rep. 2015; 64(12): 1-64.; Feng B, Zhai J, Cai Y. Effect of twin pregnancy chorionic properties on maternal and fetal outcomes. Taiwan J Obstet Gynecol. 2018; 57(3): 351-354. doi:10.1016/j.tjog.2018.03.002; Hayes-Ryan D, Meaney S, Hodnett A, Geisler M, O’Donoghue K. The maternal and perinatal implications of hypertensive disorders of pregnancy in a multiple pregnancy cohort. Acta Obstet Gynecol Scand. 2020; 99(4): 525-536. doi:10.1111/aogs.13774; Liem SMS, van Pampus MG, Mol BWJ, Bekedam DJ. Cervical pessaries for the prevention of preterm birth: A systematic review. Obstet Gynecol Int. 2013; 2013: 576723. doi:10.1155/2013/576723; McLennan AS, Gyamfi-Bannerman C, Ananth CV, Wright JD, Siddiq Z, D’Alton ME, et al. The role of maternal age in twin pregnancy outcomes. Am J Obstet Gynecol. 2017; 217(1): 80.e1-80.e8. doi:10.1016/j.ajog.2017.03.002; Martin JA, Hamilton BE, Osterman MJK. Three decades of twin births in the United States, 1980–2009. NCHS Data Brief. 2012; 80: 1-8.; Mendoza M, Ribera I, Maiz N, Goya M, Carreras E. Cervical modifications after pessary placement insingleton pregnancies with maternal short cervical length: 2D and 3D ultrasound evaluation. Acta Obstet Gynecol Scand. 2019; 98: 1442-1449. doi. 10.1111/aogs.13647; Misra DP, Ananth CV. Infant mortality among singletons and twins in the United States during 2 decades: Effects of maternal age. Pediatrics. 2002; 110(6): 1163-1168.; SMFM Research Committee; Grantz KL, Kawakita T, Lu YL, Newman R, Berghella V, Caughey A. SMFM Special Statement. State of the science on multifetal gestations: Unique considerations and importance. Am J Obstet Gynecol. 2019; 221(2): B2-B12. doi:10.1016/j.ajog.2019.04.013; Santana DS, Cecatti JG, Haddad SM, Parpinelli MA, Costa ML, Surita FG, et al. Severe maternal morbidity and perinatal outcomes of multiple pregnancy in the Brazilian Network for the Surveillance of Severe Maternal Morbidity. Int J Gynaecol Obstet. 2017; 139(2): 230-238. doi:10.1002/ijgo.12287; Romanenko TG, Sulimenko OM. Prevention of preeclampsia in women with multiple pregnancy after assisted reproduction. Wiad Lek. 2020; 73(3): 494-497.; McClure EM, Saleem S, Goudar SS, Moore JL, Garces A, Esamai F, et al. Stillbirth rates in low-middle income countries 2010–2013: A population-based, multi-country study from the Global Network. Reprod Health. 2015; 90(12): 1379-1385. doi:10.1186/1742-4755-12-S2-S7; Kalafat E, Thilaganathan B, Papageorghiou A, Bhide A, Khalil A. Significance of placental cord insertion site in twin pregnancy. Ultrasound Obstet Gynecol. 2018; 52(3): 378-384. doi:10.1002/uog.18914; Townsend R, Khalil A. Fetal growth restriction in twins. Best Pract Res Clin Obstet Gynaecol. 2018; 49: 79-88. doi:10.1016/j.bpobgyn.2018.02.004; Murray SR, Stock SJ, Cowan S, Cooper ES, Norman JE. Spontaneous preterm birth prevention in multiple pregnancy. Obstet Gynaecol. 2018; 20(1): 57-63.; Romero R, Conde-Agudelo A, El-Refaie W, Rode L, Brizot ML, Cetingoz E, et al. Vaginal progesterone decreases preterm birth and neonatal morbidity and mortality in women with a twin gestation and a short cervix: An updated meta-analysis of individual patient data. Ultrasound Obstet Gynecol. 2017; 49(3): 303-314. doi:10.1002/uog.17397; Boiko VI, Nikitina IM, Babar TV, Boiko AV. The problem of miscarriage in multiple pregnancy. Wiad Lek. 2018; 71(7): 1195-1199.; Dang VQ, Nguyen LK, Pham TD, He YTN, Vu KN, Phan MTN, et al. Pessary compared with vaginal progesterone for the prevention of preterm birth in women with twin pregnancies and cervical length less than 38 mm: A randomized controlled trial. Obstet Gynecol. 2019; 133(3): 459-467.; Barinov SV, Di Renzo GC, Belinina AA, Koliado OV, Remneva OV. Clinical and biochemical markers of spontaneous preterm birth in singleton and multiple pregnancies. J Matern Fetal Neonatal Med. 2021 Feb 24; 1-6. doi:10.1080/14767058.2021.1892064; https://www.actabiomedica.ru/jour/article/view/3541

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    Academic Journal

    Source: Reproductive health of woman; No. 1 (2021); 44-48 ; Reproductive health of woman; № 1 (2021); 44-48 ; Репродуктивне здоров'я жінки; № 1 (2021); 44-48 ; 2708-8731 ; 2708-8723

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    Academic Journal

    Source: Obstetrics, Gynecology and Reproduction; Vol 14, No 6 (2020); 602-611 ; Акушерство, Гинекология и Репродукция; Vol 14, No 6 (2020); 602-611 ; 2500-3194 ; 2313-7347

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    Relation: https://www.gynecology.su/jour/article/view/886/879; El Toukhy T., Khalaf Y., Braude P. IVF results: optimize not maximize. Am J Obstet Gynecol. 2006;194(2):322–31. https://doi.org/10.1016/j.ajog.2005.05.018.; Luke B., Brown M.B. The changing risk of infant mortality by gestation, plurality, and race: 1989–1991 versus 1999–2001. Pediatrics. 2006;118(6):2488–97. https://doi.org/10.1542/peds.2006-1824.; Luke B. Reducing fetal deaths in multiple births: optimal birthweights and gestational ages for infants of twin and triplet births. Acta Genet Med Gemellol (Roma). 1996;45(3):333–48. https://doi.org/10.1017/S0001566000000933.; Sebire N.J., Snijders R.J., Hughes K. et al. The hidden mortality of monochorionic twin pregnancies. Br J Obstet Gynaecol. 1997;104(10):1203–7. https://doi.org/10.1111/j.1471-0528.1997.tb10948.x.; Heyborne K.D., Porreco R.P., Garite T.J. et al.; Obstetrix/Pediatrix Research Study Group. Improved perinatal survival of monoamniotic twins with intensive inpatient monitoring. Am J Obstet Gynecol. 2005;192(1):96–101. https://doi.org/10.1016/j.ajog.2004.06.037.; Hack K.E., Derks J.B., Schaap A.H. et al. Perinatal outcome of monoamniotic twin pregnancies. Obstet Gynecol. 2009;113(2 Pt 1):353–60. https://doi.org/10.1097/AOG.0b013e318195bd57.; Morikawa M., Yamada T., Yamada T. et al. Prospective risk of intrauterine fetal death in monoamniotic twin pregnancies. Twin Res Hum Genet. 2012;15(4):522–6. https://doi.org/10.1017/thg.2012.30.; Beasley E., Megerian G., Gerson A., Roberts N.S. Monoamniotic twins: case series and proposal for antenatal management. Obstet Gynecol. 1999;93(1):130–4. https://doi.org/10.1016/s0029-7844(98)00399-8.; Enbom J.A. Twin pregnancy with intrauterine death of one twin. Am J Obstet Gynecol. 1985;152(4):424–9. https://doi.org/10.1016/s0002-9378(85)80152-6.; Rydhstrоm H., Ingemarsson I. Prognosis and long-term follow-up of a twin after antenatal death of the co-twin. J Reprod Med. 1993;38(2):142–6.; Ferriman E., Stratton S., Stern V. Twin pregnancy. Obstet Gynaecol Reprod Med. 2018;28(8):221–8. https://doi.org/10.1016/j.ogrm.2018.07.002.; Mackie F.L., Morris R.K., Kilby M.D. Fetal brain injury in survivors of twin pregnancies complicated by demise of one twin: a review. Twin Res Hum Genet. 2016;19(3):262–7. https://doi.org/10.1017/thg.2016.39.; Цибизова В.И., Говоров И.Е., Первунина Т.М. и др. Пренатальный скрининг первого триместра при многоплодной беременности. Часть I: сравнительный анализ сывороточных белков PAPP-A и β-ХГЧ при беременности, наступившей спонтанно или в результате экстракорпорального оплодотворения. Акушерство, Гинекология и Репродукция. 2020;14(1):25–33. https://doi.org/10.17749/2313-7347.2020.14.1.25-33.; Цибизова В.И., Говоров И.Е., Первунина Т.М. и др. Пренатальный скрининг первого триместра при многоплодной беременности. Часть II: сывороточные белки PAPP-A и β-ХГЧ как маркеры неблагоприятных исходов беременности. Акушерство, Гинекология и Репродукция. 2020;14(1):34–43. https://doi.org/10.17749/2313-7347.2020.14.1.34-4.; Цибизова В.И., Говоров И.Е., Аверкин И.И. и др. Оценка медицинских технологий в акушерстве: преимущества индивидуального консервативного ведения монохориальной беременности, осложненной синдромом обратной артериальной перфузии, перед хирургическим вмешательством. ФАРМАКОЭКОНОМИКА. Современная Фармакоэкономика и Фармакоэпидемиология. 2020;13(1):36–42. https://doi.org/10.17749/2070-4909.2020.13.1.36-42.; Smith G.C., Stenhouse E.J., Crossley J.A. et al. Early-pregnancy origins of low birth weight. Nature. 2002;417(6892):916. https://doi.org/10.1038/417916a.; Spencer C., Allen V., Flowerdew G. et al. Low levels of maternal serum PAPP-A in early pregnancy and the risk of adverse outcomes. Prenat Diagn. 2008;28(11):1029–36. https://doi.org/10.1002/pd.2116.; Liao A., Heath V., Kametas N. et al. First-trimester screening for trisomy 21 in singleton pregnancies achieved by assisted reproduction. Hum Reprod. 2001;16(7):1501–4. https://doi.org/10.1093/humrep/16.7.1501.; Maymon R., Shulman A. Serial first-and second-trimester Down's syndrome screening tests among IVF-versus naturally-conceived singletons. Hum Reprod. 2002;17(4):1081–5. https://doi.org/10.1093/humrep/17.4.1081.; Bellver J., Lara C., Soares S.R. et al. First trimester biochemical screening for Down's syndrome in singleton pregnancies conceived by assisted reproduction. Hum Reprod. 2005;20(9):2623–7. https://doi.org/10.1093/humrep/dei107.; Conover C.A., Bale L.K., Overgaard M.T. et al. Metalloproteinase pregnancy-associated plasma protein A is a critical growth regulatory factor during fetal development. Development. 2004;131(5):1187–94. https://doi.org/10.1242/dev.00997.; Lin T.-M., Halbert S.P., Kiefer D. et al. Characterization of four human pregnancy-associated plasma proteins. Am J Obstet Gynecol. 1974;118(2):223–36. https://doi.org/10.1016/0002-9378(74)90553-5.; Guibourdenche J., Frendo J., Pidoux G. et al. Expression of pregnancy-associated plasma protein-A (PAPP-A) during human villous trophoblast differentiation in vitro. Placenta. 2003;24(5):532–9. https://doi.org/10.1053/plac.2002.0944.; Dugoff L., Hobbins J.C., Malone F.D. et al. First-trimester maternal serum PAPP-A and free-beta subunit human chorionic gonadotropin concentrations and nuchal translucency are associated with obstetric complications: a population-based screening study (the FASTER Trial). Am J Obstet Gynecol. 2004;191(4):1446–51. https://doi.org/10.1016/j.ajog.2004.06.052.; Ong C.Y., Liao A.W., Spencer K. et al. First trimester maternal serum free β human chorionic gonadotrophin and pregnancy-associated plasma protein A as predictors of pregnancy complications. BJOG. 2000;107(10):1265–70. https://doi.org/10.1111/j.1471-0528.2000.tb11618.x.; Amor D.J., Xu J., Halliday J.L. et al. Pregnancies conceived using assisted reproductive technologies (ART) have low levels of pregnancyassociated plasma protein-A (PAPP-A) leading to a high rate of falsepositive results in first trimester screening for Down syndrome. Hum Reprod. 2009;24(6):1330–8. https://doi.org/10.1093/humrep/dep046.; Tul N., Novak-Antolic Z. Serum PAPP-A levels at 10–14 weeks of gestation are altered in women after assisted conception. Prenat Diagn. 2006;26(12):1206–11. https://doi.org/10.1002/pd.1589.; Lawrence J.B., Oxvig C., Overgaard M.T. et al. The insulin-like growth factor (IGF)-dependent IGF binding protein-4 protease secreted by human fibroblasts is pregnancy-associated plasma protein-A. 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    Academic Journal

    Source: Obstetrics, Gynecology and Reproduction; Vol 15, No 4 (2021); 371-378 ; Акушерство, Гинекология и Репродукция; Vol 15, No 4 (2021); 371-378 ; 2500-3194 ; 2313-7347

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