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

Year Number of Results
1967 1
1968 1
1970 2
1971 2
1972 1
1973 2
1974 3
1975 2
1976 1
1977 2
1978 1
1981 2
1982 1
1984 2
1985 1
1986 3
1987 5
1988 7
1989 5
1990 6
1991 5
1992 7
1993 13
1994 11
1995 11
1996 6
1997 11
1998 15
1999 5
2000 5
2001 10
2002 10
2003 15
2004 12
2005 6
2006 13
2007 15
2008 15
2009 15
2010 14
2011 18
2012 20
2013 17
2014 18
2015 14
2016 18
2017 13
2018 12
2019 21
2020 23
2021 22
2022 16
2023 0
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445 results
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Page 1
Hypothyroidism and hyperthyroidism.
Guerri G, Bressan S, Sartori M, Costantini A, Benedetti S, Agostini F, Tezzele S, Cecchin S, Scaramuzza A, Bertelli M. Guerri G, et al. Acta Biomed. 2019 Sep 30;90(10-S):83-86. doi: 10.23750/abm.v90i10-S.8765. Acta Biomed. 2019. PMID: 31577260 Free PMC article. Review.
Congenital hypothyroidism is a condition in which the thyroid gland does not produce enough thyroid hormones. ...Without treatment, congenital hypothyroidism leads to severe intellectual deficit and short stature. ...
Congenital hypothyroidism is a condition in which the thyroid gland does not produce enough thyroid hormones. ...Without treatment,
Prenatal diagnosis and management of omphalocele.
Verla MA, Style CC, Olutoye OO. Verla MA, et al. Semin Pediatr Surg. 2019 Apr;28(2):84-88. doi: 10.1053/j.sempedsurg.2019.04.007. Epub 2019 Apr 6. Semin Pediatr Surg. 2019. PMID: 31072463 Review.
Omphalocele (exomphalos) is one of the most common abdominal wall defects. ...The purpose of this article is to discuss the approach to prenatal diagnosis and management of omphalocele....
Omphalocele (exomphalos) is one of the most common abdominal wall defects. ...The purpose of this article is to discuss the approach
Classification of primary and incisional abdominal wall hernias.
Muysoms FE, Miserez M, Berrevoet F, Campanelli G, Champault GG, Chelala E, Dietz UA, Eker HH, El Nakadi I, Hauters P, Hidalgo Pascual M, Hoeferlin A, Klinge U, Montgomery A, Simmermacher RK, Simons MP, Smietański M, Sommeling C, Tollens T, Vierendeels T, Kingsnorth A. Muysoms FE, et al. Hernia. 2009 Aug;13(4):407-14. doi: 10.1007/s10029-009-0518-x. Epub 2009 Jun 3. Hernia. 2009. PMID: 19495920 Free PMC article. Review.
CONCLUSIONS: A classification for primary abdominal wall hernias and a division into subgroups for incisional abdominal wall hernias, concerning the localisation of the hernia, was formulated....
CONCLUSIONS: A classification for primary abdominal wall hernias and a division into subgroups for incisional abdominal wall hernias, concer …
Pediatric abdominal wall defects.
Kelly KB, Ponsky TA. Kelly KB, et al. Surg Clin North Am. 2013 Oct;93(5):1255-67. doi: 10.1016/j.suc.2013.06.016. Epub 2013 Jul 26. Surg Clin North Am. 2013. PMID: 24035087 Review.
This article reviews the incidence, presentation, anatomy, and surgical management of abdominal wall defects found in the pediatric population. Defects such as inguinal hernia and umbilical hernia are common and are encountered frequently by the pediatric sur …
This article reviews the incidence, presentation, anatomy, and surgical management of abdominal wall defects found in the pediatric populati …
Umbilical Hernia Repair: Overview of Approaches and Review of Literature.
Appleby PW, Martin TA, Hope WW. Appleby PW, et al. Surg Clin North Am. 2018 Jun;98(3):561-576. doi: 10.1016/j.suc.2018.02.001. Epub 2018 Mar 12. Surg Clin North Am. 2018. PMID: 29754622 Review.
Umbilical hernias are ubiquitous, and surgery is indicated in symptomatic patients. Umbilical hernia defects can range from small (<1 cm) to very large/complex hernias, and treatment options should be tailored to the clinical situation. ...
Umbilical hernias are ubiquitous, and surgery is indicated in symptomatic patients. Umbilical hernia defects can range
The prevalence of congenital anomalies in Europe.
Dolk H, Loane M, Garne E. Dolk H, et al. Adv Exp Med Biol. 2010;686:349-64. doi: 10.1007/978-90-481-9485-8_20. Adv Exp Med Biol. 2010. PMID: 20824455 Review.
EUROCAT (European Surveillance of Congenital Anomalies) is the network of population-based registers of congenital anomaly in Europe, with a common protocol and data quality review, covering 1.5 million annual births in 22 countries. ...Thus, congenital anoma …
EUROCAT (European Surveillance of Congenital Anomalies) is the network of population-based registers of congenital anomaly in …
Abdominal Wall Defects.
Slater BJ, Pimpalwar A. Slater BJ, et al. Neoreviews. 2020 Jun;21(6):e383-e391. doi: 10.1542/neo.21-6-e383. Neoreviews. 2020. PMID: 32482700 Review.
The 2 most common congenital abdominal wall defects are gastroschisis and omphalocele. ...The main distinguishing features between the 2 are that gastroschisis has no sac and the defect is to the right of the umbilicus, whereas an omphalocele typically has a …
The 2 most common congenital abdominal wall defects are gastroschisis and omphalocele. ...The main distinguishing features bet …
Feeding problems and gastrointestinal diseases in Down syndrome.
Ravel A, Mircher C, Rebillat AS, Cieuta-Walti C, Megarbane A. Ravel A, et al. Arch Pediatr. 2020 Jan;27(1):53-60. doi: 10.1016/j.arcped.2019.11.008. Epub 2019 Nov 26. Arch Pediatr. 2020. PMID: 31784293 Review.
RESULTS: The anomalies are grouped into three categories: anatomical anomalies: duodenal atresia and stenosis (3.9%), duodenal web and annular pancreas; aberrant right subclavian artery (12% of children with DS with cardiac anomaly); Hirschsprung's disease (2.76%); anorectal malf …
RESULTS: The anomalies are grouped into three categories: anatomical anomalies: duodenal atresia and stenosis (3.9%), duodenal web and annul …
Congenital hypothyroidism.
Rastogi MV, LaFranchi SH. Rastogi MV, et al. Orphanet J Rare Dis. 2010 Jun 10;5:17. doi: 10.1186/1750-1172-5-17. Orphanet J Rare Dis. 2010. PMID: 20537182 Free PMC article. Review.
Congenital hypothyroidism (CH) occurs in approximately 1:2,000 to 1:4,000 newborns. ...On examination, common signs include myxedematous facies, large fontanels, macroglossia, a distended abdomen with umbilical hernia, and hypotonia. CH is classified into per
Congenital hypothyroidism (CH) occurs in approximately 1:2,000 to 1:4,000 newborns. ...On examination, common signs include myxedemat
Omphalocele-What should we tell the prospective parents?
Adams AD, Stover S, Rac MW. Adams AD, et al. Prenat Diagn. 2021 Mar;41(4):486-496. doi: 10.1002/pd.5886. Epub 2021 Feb 4. Prenat Diagn. 2021. PMID: 33540475 Review.
An omphalocele is a congenital defect in the abdominal wall characterized by absent abdominal muscles, fascia, and skin. The characteristic ultrasound appearance includes a midline defect with herniation of abdominal contents into the base of the umbilical co …
An omphalocele is a congenital defect in the abdominal wall characterized by absent abdominal muscles, fascia, and skin. The c …
445 results