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Human Genetics|October 22, 2013
Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic formJulie Salomon, Olivier Goulet, Danielle Canioni, et al.Journal of Pediatric Gastroenterology and Nutrition|June 12, 2021
A European Survey on Digestive Perianastomotic Ulcerations, a Rare Crohn-like Disorder Occurring in Children and Young AdultsChrystele Madre, Mario Mašić, Daniela Prlenda-Touilleux, et al.Journal of Pediatric Gastroenterology and Nutrition|August 3, 2020
Clinical Remission and Psychological Management are Major Issues for the Quality of Life in Pediatric Crohn DiseaseAnne Gourdonneau, Léa Bruneau, Frank M Ruemmele, et al.Archives of Disease in Childhood|April 17, 2021
Feeding disorders in children with oesophageal atresia: a cross-sectional studyAurélie Pham, Emmanuelle Ecochard-Dugelay, Arnaud Bonnard, et al.Annales D'Endocrinologie|May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.Annales D'Endocrinologie|March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.Pageof 4