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1964
2025

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

Year Number of Results
1964 1
1965 1
1967 2
1968 2
1969 2
1971 1
1973 2
1974 3
1975 2
1977 1
1978 1
1982 1
1985 3
1986 1
1987 1
1988 7
1989 7
1990 6
1991 4
1992 6
1993 10
1994 10
1995 7
1996 12
1997 17
1998 10
1999 6
2000 13
2001 13
2002 5
2003 6
2004 12
2005 6
2006 7
2007 10
2008 8
2009 8
2010 12
2011 21
2012 17
2013 25
2014 17
2015 10
2016 10
2017 7
2018 7
2019 8
2020 9
2021 5
2022 7
2023 10
2024 9
2025 1

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359 results

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Page 1
VACTERL/VATER Association.
Solomon BD. Solomon BD. Orphanet J Rare Dis. 2011 Aug 16;6:56. doi: 10.1186/1750-1172-6-56. Orphanet J Rare Dis. 2011. PMID: 21846383 Free PMC article. Review.
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. ...The management of pa …
VACTERL/VATER association is typically defined by the presence of at least three of the following congenital malformations: vertebral defect …
Basic Knowledge of Tracheoesophageal Fistula and Esophageal Atresia.
Lee S. Lee S. Adv Neonatal Care. 2018 Feb;18(1):14-21. doi: 10.1097/ANC.0000000000000464. Adv Neonatal Care. 2018. PMID: 29373345 Review.
BACKGROUND: Tracheoesophageal fistula (TEF) and esophageal atresia (EA) are rare anomalies in neonates. Up to 50% of neonates with TEF/EA will have Vertebral anomalies (V), Anal atresia (A), Cardiac anomalies (C), Tracheoesophageal fistula (T), Esophageal …
BACKGROUND: Tracheoesophageal fistula (TEF) and esophageal atresia (EA) are rare anomalies in neonates. Up to 50% of neonates with TE …
Exstrophy-Epispadias Complex.
Lee T, Borer J. Lee T, et al. Urol Clin North Am. 2023 Aug;50(3):403-414. doi: 10.1016/j.ucl.2023.04.004. Epub 2023 May 19. Urol Clin North Am. 2023. PMID: 37385703 Review.
Exstrophy-epispadias complex encompasses a spectrum of disorders with lower abdominal midline malformations, including epispadias, bladder exstrophy, and cloacal exstrophy, also known as Omphalocele-Exstrophy-Imperforate Anus-Spinal Anomalies Complex. In this review …
Exstrophy-epispadias complex encompasses a spectrum of disorders with lower abdominal midline malformations, including epispadias, bladder e …
MED12 related disorders.
Graham JM Jr, Schwartz CE. Graham JM Jr, et al. Am J Med Genet A. 2013 Nov;161A(11):2734-40. doi: 10.1002/ajmg.a.36183. Epub 2013 Oct 10. Am J Med Genet A. 2013. PMID: 24123922 Free PMC article. Review.
Anorectal malformations.
Herman RS, Teitelbaum DH. Herman RS, et al. Clin Perinatol. 2012 Jun;39(2):403-22. doi: 10.1016/j.clp.2012.04.001. Clin Perinatol. 2012. PMID: 22682388 Review.
Rhomboencephalosynapsis: Review of the Literature.
Fouda MA, Kim TY, Cohen AR. Fouda MA, et al. World Neurosurg. 2022 Mar;159:48-53. doi: 10.1016/j.wneu.2021.12.062. Epub 2021 Dec 22. World Neurosurg. 2022. PMID: 34954057 Review.
Rhombencephalosynapsis can be isolated or can occur in association with other congenital anomalies and syndromes such as Gomez-Lopez-Hernandez syndrome (GLHS) or VACTERL: vertebral anomalies (V), anal atresia (A), cardiovascular defects (C), esophageal atresia
Rhombencephalosynapsis can be isolated or can occur in association with other congenital anomalies and syndromes such as Gomez-Lopez-Hernand …
Radial longitudinal deficiency.
Maschke SD, Seitz W, Lawton J. Maschke SD, et al. J Am Acad Orthop Surg. 2007 Jan;15(1):41-52. doi: 10.5435/00124635-200701000-00005. J Am Acad Orthop Surg. 2007. PMID: 17213381 Review.
All children presenting with radial longitudinal deficiency, regardless of severity, require a renal ultrasound, echocardiogram, and complete blood count to evaluate the potential for associated systemic conditions; these include Fanconi's anemia, the Holt-Oram syndrome, and the …
All children presenting with radial longitudinal deficiency, regardless of severity, require a renal ultrasound, echocardiogram, and complet …
Pediatric laparoscopy.
Harrington S, Simmons K, Thomas C, Scully S. Harrington S, et al. AORN J. 2008 Aug;88(2):211-36; quiz 237-40. doi: 10.1016/j.aorn.2008.04.002. AORN J. 2008. PMID: 18782939 Review.
Traditional surgical procedures that are now being performed laparoscopically include gastrostomy, pyloromyotomy, and repair of congenital diaphragmatic hernia and imperforate anus. All perioperative team members must be prepared to provide appropriately sized instr …
Traditional surgical procedures that are now being performed laparoscopically include gastrostomy, pyloromyotomy, and repair of congenital d …
Transanal recto-anal anastomosis for treatment of rectal atresia: a review of 4 cases.
Shehata S, ElSawaf M, Kotb M. Shehata S, et al. BMC Pediatr. 2023 Jan 28;23(1):46. doi: 10.1186/s12887-023-03859-9. BMC Pediatr. 2023. PMID: 36707784 Free PMC article. Review.
INTRODUCTION: Rectal atresia is a rare subtype of anorectal malformations in which the patients are born with a normal anal canal but have complete atresia located few centimeters proximal to the dentate line. ...METHODS: Four patients were diagnosed as havin …
INTRODUCTION: Rectal atresia is a rare subtype of anorectal malformations in which the patients are born with a normal anal ca …
Townes-Brocks syndrome.
Powell CM, Michaelis RC. Powell CM, et al. J Med Genet. 1999 Feb;36(2):89-93. J Med Genet. 1999. PMID: 10051003 Free PMC article. Review.
Major findings include external ear anomalies, hearing loss, preaxial polydactyly and triphalangeal thumbs, imperforate anus, and renal malformations. Most patients with Townes-Brocks syndrome have normal intelligence, although mental retardation has been noted in a …
Major findings include external ear anomalies, hearing loss, preaxial polydactyly and triphalangeal thumbs, imperforate anus, …
359 results