Results 311 to 320 of about 1,045,421 (416)

Incidence of biliary atresia in the United States before and during the COVID‐19 pandemic

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives The etiology of biliary atresia (BA) is unclear and potentially involves viral triggers. We aimed to compare the incidence of BA in the United States before and during the coronavirus disease 2019 (COVID‐19) pandemic, focusing on potential associations with viral circulation disruptions caused by nonpharmaceutical interventions ...
Yasmeen Z. Qwaider   +6 more
wiley   +1 more source

ESMO Clinical Practice Guideline interim update on the management of biliary tract cancer. [PDF]

open access: yesESMO Open
Vogel A   +2 more
europepmc   +1 more source

Aeroportia and pneumatosis intestinalis in infants with food protein‐induced‐allergic proctocolitis: A presentation of two cases

open access: yesJPGN Reports, EarlyView.
Abstract Bloody stools are a particularly concerning symptom in neonates and infants. The differential diagnosis reaches from life‐threatening to benign conditions. We would like to present two infants, who presented to the paediatric emergency department with bloody stools and showed pneumatosis on ultrasonography, which initially led to the suspicion
Jessica Ruesen   +5 more
wiley   +1 more source

Inflammatory bowel disease and hereditary hemochromatosis: A case series

open access: yesJPGN Reports, EarlyView.
Abstract We report a case series of three pediatric patients with inflammatory bowel disease (IBD) and variants in HFE which causes hereditary hemochromatosis (HH) type 1. Mice models suggest that these patients may be at increased risk for colitis and colon cancer. We detail the clinical course of these patients regarding IBD and iron overload and HFE‐
Jackson Fein   +3 more
wiley   +1 more source

CARCINOMA OF THE LIVER, BILIARY TRACT AND PANCREAS

open access: hybrid, 1980
土屋 凉一   +4 more
openalex   +2 more sources

Colorectal cancer in a 13‐year‐old with constitutional mismatch repair deficiency and MUTYH heterozygosity

open access: yesJPGN Reports, EarlyView.
Abstract Constitutional mismatch repair deficiency (CMMRD) is a rare hereditary cancer syndrome resulting from biallelic mutations in DNA mismatch repair (MMR) genes that lead to early‐onset cancers in children, including lymphoma and colorectal cancer (CRC).
Chloe J. Cohan   +3 more
wiley   +1 more source

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