Results 191 to 200 of about 76,819 (327)

Copper chelation therapy in intrahepatic cholestasis of childhood. [PDF]

open access: bronze, 1983
James Evans   +4 more
openalex   +1 more source

Frequency and Severity of Hyperbilirubinemia in Cats and Dogs With Septic Peritonitis or Pyothorax

open access: yesJournal of Veterinary Emergency and Critical Care, EarlyView.
ABSTRACT Objective To characterize serum total bilirubin (TBil) value within 72 h of admission in cats and dogs with septic peritonitis or pyothorax and its relationship with outcome. Design Cross‐sectional retrospective study. Setting University teaching hospital.
Frederick John Benham‐Crosswell   +3 more
wiley   +1 more source

miRNA-21 ablation protects against liver injury and necroptosis in cholestasis

open access: yesCell Death and Differentiation, 2018
M. B. Afonso   +8 more
semanticscholar   +1 more source

Assessment of metabolic dysfunction‐associated fatty liver disease in primary care: a consensus statement summary

open access: yesMedical Journal of Australia, EarlyView.
Abstract Introduction Metabolic dysfunction‐associated fatty liver disease (MAFLD) is common. This evidence‐based consensus statement summary provides recommendations for the assessment and monitoring of adults with MAFLD in primary care. Main recommendations Adults with type 2 diabetes, obesity or two or more other metabolic risk factors should be ...
Leon A Adams   +15 more
wiley   +1 more source

Enteral Nutrition in Neonatal Cholestasis: An Up-to-Date Overview. [PDF]

open access: yesNutrients
Cimadamore E   +6 more
europepmc   +1 more source

Urinary sulfated bile acid of patients with cholestasis.

open access: bronze, 1976
Isao Makino   +4 more
openalex   +2 more sources

Effectiveness of Pyridoxal‐5′‐Phosphate in PNPO Deficiency: A Systematic Review

open access: yesJournal of Inherited Metabolic Disease, Volume 48, Issue 5, September 2025.
ABSTRACT Pyridox(am)ine 5′‐phosphate oxidase (PNPO) deficiency is an ultrarare inherited neurometabolic disease, characterized by primarily neonatal‐onset B6‐responsive epileptic encephalopathies. Treatment often requires sustainable access to high‐quality pyridoxal‐5′‐phosphate (PLP, i.e., active vitamin B6), although some patients (also) respond to ...
Nina N. Stolwijk   +7 more
wiley   +1 more source

Severe hepatopulmonary syndrome with end-stage liver cirrhosis associated with pan-hypopituitarism in a pediatric patient

open access: yesJournal of Clinical and Translational Endocrinology Case Reports
Cholestasis in the neonatal period requires a prompt and thorough evaluation. Panhypopituitarism is an uncommon but known cause of cholestasis. Here we present a rare and late complication of liver disease secondary to congenital hypopituitarism ...
Shawn A. Haupt   +10 more
doaj  

Focal Nodular Hyperplasia (FNH)/FNH‐Like Lesions: An Important Potential Mimic of Relapsed Malignancy in Pediatric Cancer Patients

open access: yesPediatric Blood &Cancer, Volume 72, Issue 9, September 2025.
ABSTRACT Focal nodular hyperplasia (FNH) is a rare benign lesion of the liver, which is becoming increasingly recognized in survivors of pediatric cancer. These lesions are under‐reported, but do not require further investigation or treatment. We present two cases with unusual imaging findings consistent with an FNH/FNH‐like process after completing ...
Jonathan Abrams   +4 more
wiley   +1 more source

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