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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1981 1
1985 1
1987 1
1988 2
1990 1
1991 1
1993 1
1994 1
1996 1
1997 1
1998 5
1999 2
2000 4
2001 1
2002 4
2003 2
2004 2
2005 1
2006 2
2007 2
2008 2
2009 4
2010 7
2011 4
2012 2
2013 4
2014 6
2015 8
2016 4
2017 6
2018 3
2019 13
2020 6
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Article type
Publication date

Similar Articles for PMID: 32611568

100 results
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Page 1
Fetal Anomalies in a Pregnant Woman with a History of Hirschsprung Disease and a Tracheal Web.
Suresh S, Brewerton C, Plunkett B. Suresh S, et al. Neoreviews. 2020 Jul;21(7):e489-e494. doi: 10.1542/neo.21-7-e489. Neoreviews. 2020. PMID: 32611568 No abstract available.
Fetal health status prediction based on maternal clinical history using machine learning techniques.
Akbulut A, Ertugrul E, Topcu V. Akbulut A, et al. Comput Methods Programs Biomed. 2018 Sep;163:87-100. doi: 10.1016/j.cmpb.2018.06.010. Epub 2018 Jun 14. Comput Methods Programs Biomed. 2018. PMID: 30119860
Hirschsprung disease in a large birth cohort.
Spouge D, Baird PA. Spouge D, et al. Teratology. 1985 Oct;32(2):171-7. doi: 10.1002/tera.1420320204. Teratology. 1985. PMID: 4049274
An embryological point of view on associated congenital anomalies of children with Hirschsprung disease.
Slavikova T, Zabojnikova L, Babala J, Varga I. Slavikova T, et al. Bratisl Lek Listy. 2015;116(11):640-7. doi: 10.4149/bll_2015_126. Bratisl Lek Listy. 2015. PMID: 26621159
21-Year-Old Pregnant Woman with MODY-5 Diabetes.
Mikuscheva A, McKenzie E, Mekhail A. Mikuscheva A, et al. Case Rep Obstet Gynecol. 2017;2017:6431531. doi: 10.1155/2017/6431531. Epub 2017 Oct 15. Case Rep Obstet Gynecol. 2017. PMID: 29163993 Free PMC article.
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease.
Sampson MG, Coughlin CR 2nd, Kaplan P, Conlin LK, Meyers KE, Zackai EH, Spinner NB, Copelovitch L. Sampson MG, et al. Am J Med Genet A. 2010 Oct;152A(10):2618-22. doi: 10.1002/ajmg.a.33628. Am J Med Genet A. 2010. PMID: 20799338
Evaluation of prenatally diagnosed structural congenital anomalies.
Gagnon A; GENETICS COMMITTEE. Gagnon A, et al. J Obstet Gynaecol Can. 2009 Sep;31(9):875-881. doi: 10.1016/S1701-2163(16)34307-9. J Obstet Gynaecol Can. 2009. PMID: 19941713 Review. English, French.
HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Hirschsprung Disease.
Sepahi MA, Baraty B, Shooshtary FK. Sepahi MA, et al. Iran J Pediatr. 2010 Mar;20(1):123-6. Iran J Pediatr. 2010. PMID: 23056694 Free PMC article.
[Prenatal diagnosis of skeletal dysplasia: case report of a fetus with multiple anomalies].
Novakov Mikić A, Stojić S, Konstantinidis G, Ristivojević A, Krnojelac D. Novakov Mikić A, et al. Med Pregl. 2000 Mar-Apr;53(3-4):197-201. Med Pregl. 2000. PMID: 10965689 Croatian.
Experimental fetal endoscopic tracheal occlusion in rhesus and cynomolgus monkeys: nonhuman primate models.
Sananès N, Ruano R, Weingertner AS, Regnard P, Salmon Y, Kohler A, Miry C, Mager C, Guerra F, Schneider A, Becmeur F, Leroy J, Dimarcq JL, Debry C, Favre R. Sananès N, et al. J Matern Fetal Neonatal Med. 2015;28(15):1822-7. doi: 10.3109/14767058.2014.969234. Epub 2014 Oct 10. J Matern Fetal Neonatal Med. 2015. PMID: 25260124
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