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Hepatology Communications|May 15, 2023
Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in childrenJames E Squires, Alexander G Miethke, C Alexander Valencia, et al.Frontiers in Physiology|November 16, 2020
Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and LateralityJuhoon So, Mylarappa Ningappa, Joseph Glessner, et al.The Lancet. Gastroenterology & Hepatology|May 9, 2024
Maralixibat in progressive familial intrahepatic cholestasis (MARCH-PFIC): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trialAlexander G Miethke, Adib Moukarzel, Gilda Porta, et al.Journal of Hepatology|December 29, 2016
Host conditioning and rejection monitoring in hepatocyte transplantation in humansKyle A Soltys, Kentaro Setoyama, Edgar N Tafaleng, et al.Hepatology (Baltimore, Md.)|January 22, 2019
Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation SyndromeJohn-Paul Berauer, Anya I Mezina, David T Okou, et al.Pediatrics|December 31, 2021
Pediatric Organ Dysfunction Information Update Mandate (PODIUM) Contemporary Organ Dysfunction Criteria: Executive SummaryMelania M Bembea, Michael Agus, Ayse Akcan-Arikan, et al.Pageof 10