Results 131 to 140 of about 9,333,061 (296)

STROBE-anastomotic leakage after pull-through procedure for Hirschsprung disease

, 2018
Chunhui Peng, Yajun Chen, Wenbo Pang, Tingchong Zhang, Zengmeng Wang, Dongyang Wu, Kai Wang   +6 more
openalex   +1 more source

Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease [PDF]

, 2004
V. Ashley Cantrell, Sarah E. Owens, Ronald L. Chandler, David Airey, Kevin M. Bradley, Jeffrey R. Smith, E. Michelle Southard‐Smith   +6 more
openalex   +1 more source

Bioinformatics Prediction for Network-Based Integrative Multi-Omics Expression Data Analysis in Hirschsprung Disease [PDF]

Helena Lucena-Padros, Nereida Bravo‐Gil, Cristina Tous, Elena Rojano, Pedro Seoane, Raquel M. Fernández, Juan A. G. Ranea, Guillermo Antiñolo, Salud Borrego   +8 more
openalex   +1 more source

Investigating the Diagnostic and Risk Factors for Enterocolitis in Children with Hirschsprung’s Disease

Acta Medica Bulgarica
This study aimed to identify the clinical risk factors associated with Hirschsprung-associated enterocolitis (HAEC) in children with Hirschsprung’s disease (HD).
Askarpour S., Javaherizadeh H., Peyvasteh M., Mohammadi A., Soma Seyedsalehi S.   +4 more
doaj   +1 more source

Schwann Cells in the Aganglionic Colon of Hirschsprung Disease Can Generate Neurons for Regenerative Therapy [PDF]

, 2022
Weikang Pan, Ahmed A. Rahman, Rhian Stavely, Sukhada Bhave, Richard A. Guyer, Meredith Omer, Nicole Picard, Allan M. Goldstein, Ryo Hotta   +8 more
openalex   +1 more source

Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination

Revista Chilena de Radiología, 2012
El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1.
David Ibáñez M, Ana Vela M, Beatriz Izquierdo H, Carolina Muel G   +3 more
doaj  

Lower urinary tract symptoms and sexual functions after endorectal pull-through for Hirschsprung disease: controlled long-term outcomes

, 2017
Malla I. Neuvonen, Kristiina Kyrklund, Seppo Taskinen, Antti Koivusalo, Risto Rintala, Mikko P. Pakarinen   +5 more
openalex   +2 more sources

Hirschsprung disease-ganglioneuroblastoma syndrome [PDF]

, 2020
INSERM
openalex   +1 more source

Loss-of-function mutation of c-Ret causes cerebellar hypoplasia in mice with Hirschsprung disease and Down's syndrome [PDF]

, 2021
Nobutaka Ohgami, Akira Iizuka, Hirokazu Hirai, Ichiro Yajima, Machiko Iida, Atsuyoshi Shimada, Toyonori Tsuzuki, Mayumi Jijiwa, Naoya Asai, Masahide Takahashi, Masashi Kato   +10 more
openalex   +1 more source

Corrigendum to “Mesenchymal Stem Cells Attenuates Hirschsprung diseases-Associated Enterocolitis by Reducing M1 Macrophages Infiltration via COX-2 Dependent Mechanism” [J Pediatr Surg 59 (2024) 1498–1514]

Journal of Pediatric Surgery Open
Xinyao Meng, Jun Xiao, Jing Wang, Minxian Sun, Xuyong Chen, Luyao Wu, Ke Chen, Zejian Li, ChenZhao Feng, Didi Zhuansun, Jixin Yang, Xiaojuan Wu, Donghai Yu, Wei Li, Yonghua Niu, Ying He, Mingfa Wei, Feng Chen, Bo Xiong, Jiexiong Feng, Tianqi Zhu   +20 more
doaj   +1 more source