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Journal of Pediatric Surgery|October 20, 2021
Effect of transanastomotic feeding tubes on anastomotic strictures in patients with esophageal atresia and tracheoesophageal fistula: The Quebec experienceKathryn LaRusso, Shahrzad Joharifard, Rosa Lakabi, et al.
Frontiers in Pediatrics|April 15, 2017
Position Paper of INoEA Working Group on Long-Gap Esophageal Atresia: For Better CareDavid C van der Zee, Pietro Bagolan, Christophe Faure, et al.
BMJ Open|April 1, 2017
Development of the Brussels Infant and Toddler Stool Scale ('BITSS'): protocol of the studyYvan Vandenplas, Hania Szajewska, Marc Benninga, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 30, 2004
Bone morphogenetic protein-2 and -4 limit the number of enteric neurons but promote development of a TrkC-expressing neurotrophin-3-dependent subsetAlcmène Chalazonitis, Fabien D'Autréaux, Udayan Guha, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 24, 2018
Paediatric Intestinal Pseudo-obstruction: Evidence and Consensus-based Recommendations From an ESPGHAN-Led Expert GroupNikhil Thapar, Efstratios Saliakellis, Marc A Benninga, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|February 26, 2016
Can Monitoring Fetal Intestinal Inflammation Using Heart Rate Variability Analysis Signal Incipient Necrotizing Enterocolitis of the Neonate?Hai Lun Liu, Luca Garzoni, Christophe Herry, et al.
Gastroenterology|July 21, 2020
Glial Cell-Derived Neurotrophic Factor Induces Enteric Neurogenesis and Improves Colon Structure and Function in Mouse Models of Hirschsprung DiseaseRodolphe Soret, Sabine Schneider, Guillaume Bernas, et al.
Inflammatory Bowel Diseases|March 23, 2013
Association between the PTPN2 gene and Crohn's disease: dissection of potential causal variantsValerie Marcil, David R Mack, Vijay Kumar, et al.
Human Molecular Genetics|October 9, 2003
Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)Loïc de Pontual, Virginie Népote, Tania Attié-Bitach, et al.
HGG Advances|May 6, 2022
Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulasGuojie Zhong, Priyanka Ahimaz, Nicole A Edwards, et al.
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