Hirschsprung disease-Reference-Cited by-同舟云学术

Hirschsprung disease

Published:2023-10-12 Issue:1 Volume:9 Page:
ISSN:2056-676X
Container-title:Nature Reviews Disease Primers
language:en
Short-container-title:Nat Rev Dis Primers

Author:

Montalva Louise^ORCID,Cheng Lily S.,Kapur Raj^ORCID,Langer Jacob C.,Berrebi Dominique,Kyrklund Kristiina,Pakarinen Mikko^ORCID,de Blaauw Ivo,Bonnard Arnaud,Gosain Ankush^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

https://www.nature.com/articles/s41572-023-00465-y.pdf

Reference233 articles.

1. Best, K. E. et al. Hirschsprung’s disease prevalence in Europe: a register based study. Birth Defects Res. A Clin. Mol. Teratol. 100, 695–702 (2014).

2. Kawaguchi, A. L. et al. Management and outcomes for long-segment Hirschsprung disease: a systematic review from the APSA Outcomes and Evidence Based Practice Committee. J. Pediatr. Surg. 56, 1513–1523 (2021).

3. Fusaro, F. et al. Autologous intestinal reconstructive surgery in the management of total intestinal aganglionosis. J. Pediatr. Gastroenterol. Nutr. 68, 635–641 (2019).

4. Saxton, M. L., Ein, S. H., Hoehner, J. & Kim, P. C. W. Near-total intestinal aganglionosis: long-term follow-up of a morbid condition. J. Pediatr. Surg. 35, 669–672 (2000).

5. Chatterjee, S. & Chakravarti, A. A gene regulatory network explains RET–EDNRB epistasis in Hirschsprung disease. Hum. Mol. Genet. 28, 3137–3147 (2019).

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