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JPGN Reports|July 28, 2026
Pediatric Clostridiodes difficile infection with toxic megacolon successfully treated with fecal microbiota transplantationDana McCarney, Pamela Chen, Jenna Simes, et al.JPGN Reports|July 25, 2026
Delayed diagnosis of hereditary fructose intolerance presenting as chronic lean steatosis in an adolescentAlexandra Hurlock, Melissa Lah, Hannah Sue Hyaduck, et al.JPGN Reports|August 1, 2026
The Brazilian Alagille syndrome study: New insights from a multicenter national cohortElisa Carvalho, Gilda Porta, Irene Kazue Miura, et al.JPGN Reports|July 28, 2026
Biochemical testing and pathology reveal rare cause of pediatric acute liver failure: Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeTierra L Mosher, Kathryn S Czepiel, Matthew B Neu, et al.JPGN Reports|July 25, 2026
Functional constipation in children and young adults with Prader-Willi syndromeMelinda J Pierce, Isabella Niu, Lusine Ambartsumyan, et al.JPGN Reports|July 25, 2026
Successfully performed video capsule endoscopy in an 8-month-old infant weighing 7.5 kgPaul-Christoph Zeisler, Robert Thimme, Ulrike Teufel-Schaefer, et al.JPGN Reports|July 25, 2026
Successful treatment of eosinophilic esophagitis with upadacitinib prescribed for atopic dermatitisNathalie Nguyen, Maureen BauerJPGN Reports|July 30, 2026
A preterm neonate with infantile liver failure syndrome 1 due to leucyl-tRNA synthetase 1 gene (LARS1) mutations with a histopathologic phenotype of neonatal hemochromatosisAdrienne Bruder, Naomi Laventhal, Raja Rabah, et al.JPGN Reports|July 25, 2026
Itching for a diagnosis: Dysesthesias as an atypical presentation of Wilson disease in an adolescent-Case reportTierra L R Mosher, John Hicks, Krupa R MysorePageof 65