Email this article Early prenatal biochemical screening, present state, current problems and options
- Authors: Kascheeva T.K.1, Nikolaeva Y.A.1, Baranov V.S.1, Karpov K.R.2, Vokhmyanina N.V.2, Romanenko O.P.2
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Affiliations:
- D. O. Ott Research Institute of Obstetrics and Gynecology, Northwest Branch of the Russian Academy of Medical Sciences
- City Medical Genetic Center
- Issue: Vol 61, No 3 (2012)
- Pages: 69-74
- Section: Articles
- URL: https://bakhtiniada.ru/jowd/article/view/1289
- DOI: https://doi.org/10.17816/JOWD61369-74
- ID: 1289
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##article.viewOnOriginalSite##About the authors
Tat'yana Konstantinovna Kascheeva
D. O. Ott Research Institute of Obstetrics and Gynecology, Northwest Branch of the Russian Academy of Medical Sciences
Email: tkklpd@mail.ru
leading researcher, Doct. Biol. Sci
Yukiya Anatolevna Nikolaeva
D. O. Ott Research Institute of Obstetrics and Gynecology, Northwest Branch of the Russian Academy of Medical SciencesOB/GYN doctor
Vladislav Sergeevich Baranov
D. O. Ott Research Institute of Obstetrics and Gynecology, Northwest Branch of the Russian Academy of Medical Sciences
Email: iagmail@ott.ru
professor, chief of the Laboratory for Prenatal Diagnosis
Konstantin Romanovich Karpov
City Medical Genetic CenterDeputy Head of the Clinic, PhD
Nataliya Vasilevna Vokhmyanina
City Medical Genetic Centerchief of biochemical laboratory, Ph.D
Olga Panteleymonovna Romanenko
City Medical Genetic CenterHead of the Clinic, Doct.Med.Sci
References
- Внедрение алгоритма комбинированного скрининга хромосомной патологии плода в 1 триместре беременности. Опыт работы за 4 года / Некрасова Е. С. [и др.] // Журнал акушерства женских болезней. — 2007. — № 1. — С. 28–34.
- Итоги массового биохимического скрининга беременных в Санкт-Петербурге (2008–2009) / Кащеева Т. К. [и др.] // Молекулярно-биологические технологии в медицинской практике. Вып. 14 / ред. А. Б. Масленников. — Новосибирск, 2010. — С. 160–165.
- Николаидес К. Ультразвуковое исследование в 11–13 недель беременности. — СПб.: Петрополис, 2007. — 144 с.
- Cовременные алгоритмы пренатальной диагностики наследственных болезней: метод. пособие / Баранов В. С. [и др.]. — СПб.: Изд-во Н-Л, 2009. — 130 с.
- Cuckle H. S. Monitoring quality control of nuchal translucency // Clin. Lab. Med. — 2010. — Vol. 30. — P. 593–604.
- Danish Fetal Medicine Reseach Group. Impact of new national screening policy for Down’s screening in Denmark: population based cohort study / Ekelund C. K. [et al.] // Br. Med. J. — 2008. — Vol.337. — a2547.
- Evans M. I., Van Decruyes H., Nikolaides K. H. Nuchal translucency measurements for first trimester screening: the “price” of inaccuracy // Fetal Diag. Ther. — 2007. — Vol. 22. — P. 401–404.
- First trimester combined screening for trisomy 21 at 8–13 weeks / Wright D. [et al.] // Ultrasound Obstet. Gynecol. — 2010. — Vol. 36. — P. 404–411.
- Screening for trisomy 21 by maternal age, fetal nuchal translucency thickness, free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A / Kagan K. O. [et al.] // Ultrasound Obstet. Gynecol. — 2008. — Vol. 31. — P. 619–624
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