Results 191 to 200 of about 5,194,122 (262)
Heterogeneous effects of donor‐related risk factors in 954 pediatric liver transplantations
Abstract Objectives Accepting a suitable donor for a child awaiting pediatric liver transplantation (pLT) is increasingly challenging. Donor‐specific risk factors influence post‐transplant outcomes, but evidence in pediatric patients remains inconsistent.
Christoph Leiskau +12 more
wiley +1 more source
Role and mechanisms of cuproptosis in the pathogenesis of Wilson's disease (Review). [PDF]
Chen H +6 more
europepmc +1 more source
Abstract Objectives The identification of novel noninvasive diagnostic and prognostic biomarkers for pediatric inflammatory bowel disease (PIBD), including pediatric Crohn's disease (pCD) and ulcerative colitis (pUC), is crucial for improving therapeutic outcomes.
Tereza Pinkasova +11 more
wiley +1 more source
Prebiotic Effects of <i>Lycium barbarum</i> Polysaccharides on Gut Microbiota and Short-Chain Fatty Acids Production in Wilson's Disease: An In Vitro Fermentation Study. [PDF]
Fang S +6 more
europepmc +1 more source
Abstract Objectives The efficacy of cystic fibrosis transmembrane conductance regulator (CFTR)‐modulator therapies in preventing or ameliorating cystic fibrosis liver disease (CFLD) by correcting CFTR in cholangiocytes is not well‐documented. This study aimed to assess liver function during CFTR‐modulators.
Laura Giugliano +12 more
wiley +1 more source
Attenuated dietary motivation in Wilson's disease correlates with clinical severity. [PDF]
Wang XQ +6 more
europepmc +1 more source
Abstract Hereditary fructose intolerance (HFI) typically presents in infancy with acute metabolic crisis upon the introduction of fructose. We report a case of a 13‐year‐old female with chronic abdominal pain, short stature, and persistent mild transaminitis.
Alexandra Hurlock +4 more
wiley +1 more source
Plasma Glial Fibrillary Acidic Protein Correlates With Brain Metal Burden in Wilson's Disease. [PDF]
Fan SP +12 more
europepmc +1 more source
Abstract Hyperornithinemia‐hyperammonemia‐homocitrullinuria (HHH) syndrome is a rare metabolic condition that can cause lethargy, ataxia, tachypnea, nausea, vomiting, seizures, coma, and acute liver failure. We present a 26‐month‐old female with acute liver failure who was diagnosed with HHH 1 week after admission. Histology revealed an acute hepatitic
Tierra L. Mosher +6 more
wiley +1 more source
Suspected fibrosing cholestatic hepatitis in an immunocompetent child with hepatitis C: Case report
Abstract A 12‐year‐old boy presented to our center with elevated aminotransferases, jaundice, right upper quadrant tenderness, and hepatomegaly. Evaluation revealed a highly elevated blood hepatitis C virus (HCV) ribonucleic acid (RNA) level, and liver biopsy showed canalicular and intrahepatic cholestasis, feathery degeneration of hepatocytes, and ...
Sara Bohon +5 more
wiley +1 more source

