Results 291 to 300 of about 829,213 (404)

Vanishing bile duct syndrome

open access: yesJournal of British Surgery, 1992
P, Burra, E, Elias
openaire   +2 more sources

Rapunzel syndrome: Trichobezoar‐induced pancreatitis unraveled

open access: yesJPGN Reports, EarlyView.
Abstract Trichobezoars are rare hair‐based intraluminal foreign bodies that may cause significant gastrointestinal complications, particularly when extending into the duodenum as in Rapunzel syndrome. We report the case of an 11‐year‐old girl with sensory processing difficulties and undiagnosed avoidant/restrictive food intake disorder (ARFID), who ...
Halen Scott   +4 more
wiley   +1 more source

Vitamin B12 deficiency in a pediatric patient with gastric obstruction and jejunal feeding dependence: A case report

open access: yesJPGN Reports, EarlyView.
Abstract Pediatric B12 deficiency is most caused by insufficient dietary intake, malabsorption or autoimmune gastritis. We present a unique case of B12 deficiency in a pediatric patient with complex gastrointestinal anatomy and jejunal nutritional dependence nearly two decades after unsuccessful surgical intervention.
Angela H. Nguyen   +2 more
wiley   +1 more source

Can artificial intelligence pass the test? Evaluating chatbot scores on pediatric gastroenterology board‐style questions

open access: yesJPGN Reports, EarlyView.
Abstract Objectives The American Academy of Pediatrics (AAP) Pediatrics Review and Education Program (PREP)® Gastroenterology (GI) Self‐Assessments help pediatric gastroenterologists and trainees prepare for subspecialty board exams by providing peer‐reviewed questions and critiques based on American Board of Pediatrics content specifications.
Annette G. Roberts   +5 more
wiley   +1 more source

Effect of 103 pd radioactive stent on apoptosis of smooth muscle cells in bile duct and expression of caspase-3, Fas and bcl-2 gene in dogs

open access: hybrid, 2005
Guijin He   +8 more
openalex   +1 more source

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea

open access: yesJPGN Reports, EarlyView.
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno   +7 more
wiley   +1 more source

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