Sovremennye predstavleniya o roli polimorfizmov genov v razvitii oslozhneniy beremennosti (obzor literatury)


Cite item

Full Text

Abstract

About the authors

M V Sannikova

References

  1. Кадурина Т.И. Наследственные коллагенопатии (клиника, диагностика, лечение и диспансеризация). СПб.: Невский диалект, 2000.
  2. Кадурина Т.И., Горбунова В.Н. Вопросы терминологии и классификации дисплазии соединительной ткани. Омский науч. вестн. 2005; 5: 5-7.
  3. Козлов П.В. Преждевременный разрыв плодных оболочек при недоношенной беременности. (Прогнозирование. Тактика ведения. Перинатальные исходы). Автореф. дис. ... д-ра мед. наук. М., 2010; с. 40.
  4. Козловская И.А. Особенности клинического течения срочных родов при преждевременном излитии околоплодных вод. Автореф. дис. ... канд. мед. наук. Иркутск, 2009; с. 133.
  5. Радзинский В.Е., Милованов А.П. Экстраэмбриональные и околоплодные структуры при нормальной и осложненной беременности: Коллективная монография. М.: Медицинское информационное агентство, 2004.
  6. Сидельникова В.М., Сухих Г.Т. Невынашивание беременности: Руководство для практикующих врачей. М.: Медицинское информационное агентство, 2010.
  7. Сухих Г.Т., Ванько Л.В. Иммунология беременности. М.: Изд-во РАМН, 2003.
  8. Тоноян Л.А. Акушерская тактика при преждевременном излитии околоплодных вод. Журн. РОАГ. 2009; 1: 18-22.
  9. Andraweera P, Thompson S, Zhang V et al. Maternal, paternal and fetal single nucleotide polymorphisms in vascular endothelial growth factor family genes associate with pregnancy complications. Am J Obstet Gynecol 2009; 201 (6): S13.
  10. Andraweera PH, Dekker GA, Thompson SD et al. Association of vascular endothelial growth factor +936 C/T single-nucleotide polymorphism with pregnancies complicated by small-for-gestational-age babies. Arch Pediatr Adolesc Med 2011; 165 (12): 1123-30.
  11. Andraweera PH, Dekker GA, Thompson SD, Roberts CT. Single-Nucleotide Polymorphisms in the KDR Gene in Pregnancies Complicated by Gestational Hypertensive Disorders and Small-for-Gestational-Age Infants. Reprod Sci 2012.
  12. Anuma EA, Hilla LD, Pandyab A, Strauss JF. Connective Tissue and Related Disorders and Preterm Birth: Clues to Genes Contributing to Prematurity. Placenta 2009; 30 (3): 207-15.
  13. Barros FC, Velez Mdel P. Temporal trends of preterm birth subtypes and neonatal outcomes. Obstet Gynecol 2006; 107 (5): 1035-41.
  14. Benirschke K, Kaufmann P, Baergen R. Pathology of the human placenta. Springer, 2006.
  15. Caughey AB, Robinson JN, Norwitz ER. Contemporary diagnosis and management of preterm premature rupture of membranes. Rev Obstet Gynecol 2008; 1 (1): 11-22.
  16. Joyce EM, Moore JJ, Sacks MS. Biomechanics of the fetal membrane prior to mechanical failure: review and implications. Eur J Obstet Gynecol Reprod Biol 2009; 144 (Suppl. 1): S121-7.
  17. Lind J, Wallenburg HC. The Marfan syndrome and pregnancy: a retrospective study in a Dutch population. Eur J Obstet Gynecol Reprod Biol 2001; 98 (1): 28-35.
  18. Menon R. Spontaneous preterm birth, a clinical dilemma: etiologic, pathophysiologic and genetic heterogeneities and racial disparity. Acta Obstet Gynecol Scand 2008; 87 (6): 590-600.
  19. Menon R, Velez DR, Morgan N et al. Genetic regulation of amniotic fluid TNF-alpha and soluble TNF receptor concentrations affected by race and preterm birth. Hum Genet 2008; 124 (3): 243-53.
  20. Nystrom MJ, Caughey AB, Lyell DJ et al. Perinatal outcomes among Asian-white interracial couples. Am J Obstet Gynecol 2008; 199 (4): 385 e381-5.
  21. Parry S, Strauss JF. 3rd Premature rupture of the fetal membranes. N Engl J Med 1998; 338 (10): 663-70.
  22. Parry S, Strauss JF. Premature rupture of the fetal membranes. New Eng J Med 2006; 338 (10).
  23. Parry S, Strauss JF, Merser BM. Preterm birth, prevention and management. Blackwell Publishing LTD, 2010.
  24. Rey G, Skowronek F, Alciaturi J et al. Toll receptor 4 Asp299Gly polymorphism and its association with preterm birth and premature rupture of membranes in a South American population. Mol Hum Reprod 2008; 14 (9): 555-9.
  25. Romero R, Friel LA, Velez Edwards DR et al. A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM). Am J Obstet Gynecol 2010; 203 (4): 361 e361-361 e330.
  26. Romero R, Velez Edwards DR, Kusanovic JP et al. Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes. Am J Obstet Gynecol 2010; 202 (5): 431 e431-4.
  27. Rossiter JP, Repke JT, Morales AJ et al. A prospective longitudinal evaluation of pregnancy in the Marfan syndrome. Am J Obstet Gynecol 1995; 173 (5): 1599-606.

Copyright (c) 2012 Sannikova M.V.

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies