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The American Journal of Gastroenterology|August 26, 2010
Outcome in cystic fibrosis liver diseaseMarion Rowland, Charles G Gallagher, Risteard O'Laoide, et al.Mucosal Immunology|September 27, 2019
Colitis susceptibility in mice with reactive oxygen species deficiency is mediated by mucus barrier and immune defense defectsGabriella Aviello, Ashish K Singh, Sharon O'Neill, et al.Journal of Pediatric Gastroenterology and Nutrition|February 23, 2023
Mucosal Atrophy Predicts Poorer Outcomes in Pediatric Ulcerative Colitis-A National Inception Cohort StudyEmily Stenke, Lorraine Stallard, Sarah Cooper, et al.Inflammatory Bowel Diseases|March 4, 2025
Higher-Dose Infliximab Induction Achieves Better Maintenance Trough Levels in a National Pediatric IBD Cohort-A Retrospective StudyEmily Stenke, Dahlal Alhassan, Molly Moclair, et al.Molecular Genetics and Metabolism|May 22, 2012
Identification of a mutation in LARS as a novel cause of infantile hepatopathyJillian P Casey, Paul McGettigan, Niamh Lynam-Lennon, et al.Pediatric Research|May 2, 2020
Repeatability of transient elastography in childrenMarion Rowland, Allison McGee, Annemarie Broderick, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 12, 2014
Outcome in patients with cystic fibrosis liver diseaseMarion Rowland, Cliona Gallagher, Charles G Gallagher, et al.Infection and Immunity|May 30, 2013
Divergent mechanisms of interaction of Helicobacter pylori and Campylobacter jejuni with mucus and mucinsJulie Ann Naughton, Karina Mariño, Brendan Dolan, et al.Human Genetics|September 8, 2022
Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathyDina Marek-Yagel, Emily Stenke, Ben Pode-Shakked, et al.Journal of Inherited Metabolic Disease|April 29, 2015
Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARSJillian P Casey, Suzanne Slattery, Melanie Cotter, et al.Pageof 6