Congenital Generalized Hypoganglionosis: Clinical Aspect
Publisher
Springer Singapore
Reference14 articles.
1. Taguchi T, Ieiri S, Miyoshi K, Kohashi K, Oda Y, Kubota A, et al. The incidence and outcome of allied disorders of Hirschsprung’s disease in Japan: results from a nationwide survey. Asian J Surg. 2017;40(1):29–34.
https://doi.org/10.1016/j.asjsur.2015.04.004
.
2. Watanabe Y, Kanamori Y, Uchida K, Taguchi T. Isolated hypoganglionosis: results of a nationwide survey in Japan. Pediatr Surg Int. 2013;29(11):1127–30.
https://doi.org/10.1007/s00383-013-3378-5
.
3. Watanabe Y, Sumida W, Takasu H, Oshima K, Kanamori Y, Uchida K, et al. Early jejunostomy creation in cases of isolated hypoganglionosis: verification of our own experience based on a national survey. Surg Today. 2015;45(12):1509–12.
https://doi.org/10.1007/s00595-015-1114-6
.
4. Kapur RP, Kennedy AJ. Histopathologic delineation of the transition zone in short-segment Hirschsprung disease. Pediatr Dev Pathol. 2013;16(4):252–66.
https://doi.org/10.2350/12-12-1282-oa.1
.
5. White FV, Langer JC. Circumferential distribution of ganglion cells in the transition zone of children with Hirschsprung disease. Pediatr Dev Pathol. 2000;3(3):216–22.