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Journal of Pediatric Surgery|September 10, 2008
Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidyJacqueline Allotey, Florence Lacaille, Melissa M Lees, et al.Human Pathology|April 4, 2016
Multiple β-catenin mutations in hepatocellular lesions arising in Abernethy malformationTracy Sorkin, Sandra Strautnieks, Pierre Foskett, et al.Hepatobiliary & Pancreatic Diseases International : HBPD INT|December 15, 2015
Pigmented well-differentiated hepatocellular neoplasm with beta-catenin mutationLara Neves Souza, Rodrigo Bronze de Martino, Richard Thompson, et al.Hepatology Communications|July 27, 2022
Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1Jeremy S Nayagam, Pierre Foskett, Sandra Strautnieks, et al.The Journal of Pediatrics|June 25, 2018
Reduced Hepatocellular Expression of Canalicular Transport Proteins in Infants with Neonatal Cholestasis and Congenital HypopituitarismTassos Grammatikopoulos, Maesha Deheragoda, Sandra Strautnieks, et al.Journal of Pediatric Gastroenterology and Nutrition|April 28, 2006
Exocrine pancreatic function in children with progressive familial intrahepatic cholestasis type 2Jaroslaw Walkowiak, Irena Jankowska, Joanna Pawlowska, et al.Journal of Pediatric Gastroenterology and Nutrition|February 20, 2024
Clinical outcomes of ABCB4 heterozygosity in infants and children with cholestatic liver diseaseRobert Hegarty, Olivia Gurra, Jenneh Tarawally, et al.Journal of Pediatric Gastroenterology and Nutrition|October 19, 2020
Cholestasis Due to USP53 DeficiencyLaura N Bull, Rebecca Ellmers, Pierre Foskett, et al.World Journal of Clinical Cases|May 28, 2021
Progressive familial intrahepatic cholestasis - farnesoid X receptor deficiency due to NR1H4 mutation: A case reportPiotr Czubkowski, Richard J Thompson, Irena Jankowska, et al.Liver Cancer|August 20, 2025
High Frequency of CTNNB1 Variants Associated with Benign and Malignant Liver Tumors in Patients with Congenital Porto-Systemic ShuntsAthanasios Tyraskis, Yoh Zen, Sandra Strautnieks, et al.Pageof 2