Диссертация (1174365), страница 20
Текст из файла (страница 20)
33. – № 11. – P. 1095-1101.32.Bãlãnescu, R.N., Topor, L., Moga A. Anomalies Associated with AnorectalMalformations / R.N. Bãlãnescu, L. Topor, A. Moga // Chirurgia. – 2013. – Vol. 108. –№ 1. – P. 38-42.33.Bankier, A., Brady, J., Myers, N.A. Epidemiology and genetics / A. Bankier,J.
Brady, N.A. Myers // Oesophageal atresia / eds. S.W. Beasley, N.A. Myers, A.W.Auldist. – London: Chapman and Hall, 1991 – P. 19-29.34.Bax, K.N., Roskott, A.M., van der Zee, D.C. Esophageal atresia withoutdistal tracheoesophageal fistula: high incidence of proximal fistula / K.N. Bax, A.M.Roskott, D.C. van der Zee // J Pediatr Surg. – 2008. – Vol. 43. – № 3. – P. 522-525.35.Bednarczyk, D., Sasiadek, M., Smigiel, R. Chromosome aberrations andGene mutations in Patients with esophageal atresia / D. Bednarczyk, M. Sasiadek, R.Smigiel // JPGN.
– 2013. – Vol. 57. – № 6. – P. 688-693.36.Bilateral microphthalmia, esophageal atresia, and cryptorchidism: theanophthalmia-esophagealgenital syndrome / D. Shah, R. Jones, H. Porter, P. Turnpenny// Am J Med Genet. – 1997. – Vol. 70. – № 2. – P. 171-173.37.Birth defects. Report by the Secretariat. 63rd World Health Assembly. –38.Birth outcomes of patients with isolated anorectal malformations: A2010.population-based case-control study / G. Vermes, D. László, A.E. Czeizel [et al.] //Congenital Anomalies – 2016. – Vol.
56. – № 1. – P. 41-47.39.Blomberg M.I., Kаllen, B. Maternal obesity and morbid obesity: the risk forbirth defects in the offspring / M.I. Blomberg, B. Kаllen // Birth Defects Res A Clin MolTeratol. – 2010 – Vol. 88. – № 1. – P. 35-40.40.Brunner, H.G., van Bokhoven, H. Genetic players in esophageal atresia andtracheoesophageal fistula / H.G. Brunner, H.
van Bokhoven // Curr Opin Genet Dev. –2005. – Vol. 15. – № 3. – P. 341-347.11341.Casaccia, G., Catalano, O.A., Bagolan, P. Congenital gastrointestinalanomalies in anorectal malformations: what relationship and management? / G. Casaccia,O.A. Catalano, P. Bagolan // Congenit Anom (Kyoto). – 2009. – Vol. 49. – № 2. – P. 9396.42.Cavalli, G., Paro, R. Chromo-domain proteins: linking chromatin structureto epigenetic regulation / G.
Cavalli, R. Paro // Curr Opin Cell Biol. – 1998. – Vol. 10. –№ 3. – P. 354-360.43.CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7gene / M. Jongmans, R. Admiraal, K. van der Donk [et al.] // J Med Genet. – 2005 –Vol.43. – № 4. – P. 306-314.44.Cho, S., Moore, S.P., Fangman, T. One hundred three consecutive patientswith anorectal malformations and their associated anomalies / S.
Cho, S.P. Moore, T.Fangman // Arch Pediatr Adolesc Med. – 2001. – Vol. 155. – № 5. – P. 587-591.45.Clinical and etiological heterogeneity in patients with tracheoesophagealmalformations and associated anomalies / E. Brosens, M. Ploeg, Y. van Bever [et al.] //European J of Medical Genetics. – 2014. – Vol. 57. – № 8. – P. 440-452.46.Comparative epidemiology of selected midline congenital abnormalities / P.Yang, M.J. Knoury, W.F. Stewart [et al.] // Genet Epidemiol.
– 1994. – Vol. 11. – № 2.– P. 141-154.47.Comparison in the incidence of anorectal malformations between a first- andthird-world referral center / A.P. Theron, G. Brisighelli, A.E. Theron [et al.] // PediatrSurg Int. – 2015. – Vol. 31. – № 8. – P. 759-764.48.Comparison of environmental risk factors for esophageal atresia, anorectalmalformations, and the combined phenotype in 263 German families / N. Zwink, V.Choinitzki, F. Baudisch [et al.] // Dis Esophagus. – 2016. – Vol.
29. – № 8. – P. 10321042.49.Congenital malformations in infants born after in vitro fertilization inSweden / B. Källén, O. Finnström, A. Lindam [et al.] // Birth Defects Res A. – 2010. –Vol. 88. – № 3. – P. 137-143.11450.Congenital malformations in twins: an international study / P.Mastroiacovo, E.E. Castilla, C. Arpino [et al.] // Am J Med Genet. – 1999. – Vol. 83.
–№ 2. – P. 117-124.51.Congenital malformations of offspring of Hispanic and African-Americanwomen in California, 1989-1997 / S.L. Carmichael, G.M. Shaw, Z. Kaidarova [et al.] //Birth Defects Res. A Clin Mol Teratol. – 2004. – Vol. 70.
– № 6. – P. 382-388.52.Cuschieri, A. EUROCAT Working Group, Descriptive Epidemiology ofIsolated Anal Anomalies: A Survey of 4.6 Million Birth in Europe / A. Cuschieri // Am JMed Genet. – 2001. – Vol. 103. – № 3. – P. 207-215.53.Dennis, N.R., Nicholas, J.L., Kovar, I. Oesophageal atresia: 3 cases in 2generations / N.R. Dennis, J.L. Nicholas, I. Kovar // Arch. Dis.
Child. – 1973. – Vol. 48.– № 12. – P. 980-982.54.Depaepe, A., Dolk, H., Lechat, M.F. The epidemiology of tracheo‐oesophageal fistula and oesophageal atresia in Europe. EUROCAT Working Group / A.Depaepe, H. Dolk, M.F. Lechat // Arch Dis Child.
– 1993. – Vol. 68. – № 6. – P. 743748.55.Diabetes mellitus and birth defects / A. Correa, S.M. Gilboa, L.M. Besser [etal.] // Am J Obstet Gynecol. – 2008. – Vol. 199. – № 3. – P. 237-239.56.Down-regulationof SHH/BMP4SignallinginHumanAnorectalMalformations / J. Zhang, Z.B. Zhang, H. Gao [et al.] // J Int MedRes.
– 2009. – Vol. 37.– № 6. – P. 1842-1850.57.Eghbalian, F., Monsef, A., Mousavi-Bahar, S.H. Urinary tract and otherassociated anomalies in newborns with esophageal atresia / F. Eghbalian, A. Monsef, S.H.Mousavi-Bahar // Urol J. – 2009. – Vol. 6. – № 2. – P.
123-126.58.Epidemiology of esophageal atresia / R. Sfeir, L. Michaud, J. Salleron [etal.] // Diseases of the Esophagus. – 2013. – Vol. 26. – № 4. – P. 354-355.59.Esophageal atresia in the Northern Region Congenital Anomaly Survey,1985-1997: prenatal diagnosis and outcome / C. Sparey, G. Jawaheer, A.M. Barrett [etal.] // Am J Obstet Gynecol.
– 2000. – Vol. 182. – № 2. – P. 427-43111560.Esophageal atresia with distal fistula – unusual case series. Considerationsrelated to epidemiological aspects, malformative associations, and prenatal diagnosis /M.L. Ognean, L.C. Zgârcea, L. Bălănescu [et al.] // Rom J Morphol Embryol. – 2017. –Vol. 58.
– № 3. – P. 1069-1076.61.Esophageal atresia: Data from a national cohort / R. Sfeir, A. Bonnard, N.Khen-Dunlop [et al.] // Journal of Pediatric Surgery. – 2013. – Vol. 48. – № 8. – P. 16641669.62.Ethen, M.K., Canfield, M.A. Impact of including elective pregnancyterminations before 20 weeks gestation on birth defects rates / M.K. Ethen, M.A. Canfield// Teratology. – 2002. – Vol. 66. – № 1. – P. S32-35.63.Etiology of esophageal atresia and tracheoesophageal fistula: “mind the gap”/ E.M. de Jong, J.F. Felix, A.
de Klein [et al.] // Curr Gastroenterol Rep. – 2010. – Vol.12. – № 3. – P. 215-222.64.EUROCAT [Electronic resource]: official website. – Mode of access:www.eurocat-network.eu.65.EUROCAT Guide 1.3. [Electronic resource] // EUROCAT working group.– Mode of access: http://www.eurocat-network.eu/ content/EUROCAT-Guide-1.3.pdf.66.EUROCATEUROCAT Statistical Monitoring Report – 2007 [Electronic resource] //workinggroup.–Modeofaccess:http://www.eurocat-network.eu/content/Stat-Mon-Report-2007.pdf.67.EUROCAT Working Group: oesophageal atresia: prevalence, prenataldiagnosis and associated anomalies in 23 European regions / R.N. Pedersen, E.
Calzolari,S. Husby [et al.] // Arch Dis Child. – 2012. – Vol. 97. – № 3. – P. 227-232.68.European surveillance of congenital anomalies: EUROCAT [Electronicresource]: official website. – Mode of access: http://www.eurocatnetwork.eu/.69.Evidence That Polymorphic Deletion of theGlutathione S-TransferaseGene, GSTM1, is Associated with Esophageal Atresia / L. Filonzi, C. Magnani, G.L. deAngelis [et al.] // Birth Defects Research. – 2010. – Vol. 88 (Part A). – P. 743-747.11670.Familial congenital esophageal atresia: personal case report and review ofthe literature / M.
Van Staey, S. De Bie, M.T. Matton [et al.] // Hum. Genet. – 1984. –Vol. 66. – № 2-3. – P. 260-266.71.Familial occurrence of esophageal atresia with and without tracheoesophagel(sic) fistula: report of two unusual kindreds / B.A. Pletcher, J.S. Friedes, W.R. Breg [etal.] // Am.
J. Med. Genet. – 1991. – Vol. 39. – № 4. – P. 380-384.72.Familialrecurrenceoftracheoesophagealfistulaandassociatedmalformations / K.P. McMullen, P.S. Karnes, C.R. Moir, V.V. Michels // Am J MedGenet. – 1996. – Vol. 63. – № 4. – P. 525-528.73.First results of a European multi-center registrt of patients with anorectalmalformations / I.
de Blaauw, C.H.W. Wijers, E. Schmideke, S. Holland-Cunz [et al.] //J Pediatr Sugr. – 2013. – Vol. 48. – № 12. – P. 2530-2535.74.Forrester, M.B., Merz, R.D. Descriptive epidemiology of anal atresia inHawaii, 19861999 / M.B. Forrester, R.D. Merz // Teratology. – 2002. – Vol. 66. – Suppl.1. – P. S12-S16.75.Forrester, M.B., Merz, R.D. Epidemiology of esophageal atresia andtracheoesophageal fistula in Hawaii, 19862000 / M.B. Forrester, R.D. Merz // PublicHealth.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
