Rectal suction biopsy for the diagnosis of Hirschsprung’s disease: a systematic review of diagnostic accuracy and complications
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00383-015-3742-8.pdf
Reference68 articles.
1. Best KE, Addor MC, Arriola L et al (2014) Hirschsprung’s disease prevalence in Europe: a register based study. Birth Defects Res A Clin Mol Teratol 100(9):695–702
2. Best KE, Glinianaia SV, Bythell M et al (2012) Hirschsprung’s disease in the North of England: prevalence, associated anomalies, and survival. Birth Defects Res A Clin Mol Teratol 94(6):477–480
3. Martucciello G (2008) Hirschsprung’s disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench. Eur J Pediatr Surg 18(3):140–149
4. Barshack I, Fridman E, Goldberg I et al (2004) The loss of calretinin expression indicates aganglionosis in Hirschsprung’s disease. J Clin Pathol 57(7):712–716
5. Meier-Ruge W, Lutterbeck PM, Herzog B et al (1972) Acetylcholinesterase activity in suction biopsies of the rectum in the diagnosis of Hirschsprung’s disease. J Pediatr Surg 7(1):11–17
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