Results 281 to 290 of about 236,526 (353)

Agreement Between Magnetic Resonance Imaging Proton Density Fat Fraction Measurements and Pathologist-Assigned Steatosis Grades of Liver Biopsies From Adults With Nonalcoholic Steatohepatitis.

open access: yesGastroenterology, 2017
M. Middleton   +14 more
semanticscholar   +1 more source

Association of maternal biliary disease with hepatopancreatobiliary morbidity in offspring

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Maternal biliary disease is common, but the link with offspring hepatopancreatobiliary disease has not been studied. We assessed the association between maternal biliary disease and pediatric hepatopancreatobiliary morbidity. Methods We conducted a retrospective cohort study of 1,271,864 children born between 2006 and 2022 in Quebec,
Nathalie Auger   +6 more
wiley   +1 more source

High resolution MR Elastography to diagnose liver fibrosis and hepatic steatosis in rats

open access: green, 2007
Najat Salameh   +6 more
openalex   +1 more source

Odevixibat after liver transplant in patients with progressive familial intrahepatic cholestasis type 1: A case series

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Patients with progressive familial intrahepatic cholestasis type 1 (PFIC1) who have undergone liver transplantation (LT) may have unmet needs and impacts on daily life due to post‐LT complications, including diarrhea and hepatic steatosis.
Georg‐Friedrich Vogel   +13 more
wiley   +1 more source

Drug‐induced liver injury associated with selective androgen receptor modulators in an adolescent patient

open access: yesJPGN Reports, EarlyView.
ABSTRACT Selective androgenic receptor modulators (SARMs) have similar properties to anabolic steroids but bind to androgen receptors in a tissue‐specific manner. Studies have investigated the benefits of SARMs in promoting bone and muscle growth while limiting the adverse effects of androgenic stimulation of other organs.
David J. Katibian   +3 more
wiley   +1 more source

Hereditary hypofibrinogenemia: A rare cause of chronic liver disease

open access: yesJPGN Reports, EarlyView.
Abstract Hypofibrinogenemia is characterized by low levels of fibrinogen with patients commonly presenting asymptomatically. This report discusses a case of hereditary hypofibrinogenemia manifesting as chronic liver disease in a 2‐year‐old male who was evaluated for elevated liver enzymes and skin/soft tissue bleeding.
Hannah Caringal   +4 more
wiley   +1 more source

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