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Gastroenterology|February 19, 2013
Genetic defects in bile acid conjugation cause fat-soluble vitamin deficiencyKenneth D R Setchell, James E Heubi, Sohela Shah, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 6, 2017
Hepatic Hilar Lymph Node Reactivity at Kasai Portoenterostomy for Biliary Atresia: Correlations With Age, Outcome, and Histology of Proximal Biliary RemnantK E Bove, R Sheridan, L Fei, et al.
The American Journal of Surgical Pathology|September 25, 2018
Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and OutcomeKevin E Bove, Andrew D Thrasher, Robert Anders, et al.
The American Journal of Surgical Pathology|October 25, 2016
Key Histopathologic Features of Liver Biopsies That Distinguish Biliary Atresia From Other Causes of Infantile Cholestasis and Their Correlation With Outcome: A Multicenter StudyPierre Russo, John C Magee, Robert A Anders, et al.
The European Physical Journal. E, Soft Matter|November 26, 2021
Advances in the study of supercooled waterPaola Gallo, Johannes Bachler, Livia E Bove, et al.
Hepatology (Baltimore, Md.)|August 19, 2007
Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancyLee-Jun C Wong, Nicola Brunetti-Pierri, Qing Zhang, et al.
Arthritis and Rheumatism|October 2, 2007
International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trialsLucy R Wedderburn, Hemlata Varsani, Charles K C Li, et al.
Annals of the Rheumatic Diseases|September 26, 2013
Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of diseaseHemlata Varsani, Susan C Charman, Charles K Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2024
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinomaMengqi Ma, Mythily Ganapathi, Yiming Zheng, et al.
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