Journal Updates


Re-evaluation of King's Wilson Index in Children with Acutely Decompensated Hepatic Wilson Disease
Clinical value of surveillance biopsies in pediatric liver transplantation
Gamma-glutamyl transpeptidase-to-platelet ratio as a biomarker of liver disease and hepatic fibrosis severity in paediatric...
Body composition correlates with laboratory parameters and disease severity in infants with biliary atresia
Enabling successful transition-Evaluation of a transition to adult care program for pediatric liver transplant recipients
Extensive solitary lymphatic malformation of the liver in a child: a case report and literature reviewv
Serum Proteomics Uncovers Biomarkers of Clinical Portal Hypertension in Children With Biliary Atresia
Non-Invasive Approaches to Estimate Liver Steatosis and Stiffness in Children with Non-Alcoholic Fatty Liver Disease
Impaired Neurocognitive Performance in Children After Liver Transplantation
Not everything that counts can be counted: Tracking long-term outcomes in pediatric liver transplant recipients
COVID-19 infection in a child following liver transplantatio
Live Virus Vaccination Following Pediatric Liver Transplantation: Outcomes from Two Academic Children's Hospital


Comparison of Triglyceride Glucose (TyG) Index and Modified TyG Indices to Predict Non-Alcoholic Fatty Liver Disease in Youth
Single-center experience in management of progressive familial intrahepatic cholestasis
Sarcopenia is highly prevalent in children with autoimmune liver diseases and is linked to visceral fat and parent-perceived...
Liver Involvement in SARS-CoV-2 Vertically Infected Newborn: A Case Report
The Genetics of Inherited Cholestatic Disorders in Neonates and Infants: Evolving Challenges
Atypical manifestations of acute viral hepatitis A in children in Bangladesh: Are these really uncommon?
Characteristics of the Gut Microbiome and IL-13/TGF-β1 Mediated Fibrosis in Post-Kasai Cholangitis of Biliary Atresia
Distinctive Features of Hepatic Steatosis in Children: Is It Primary or Secondary to Inborn Errors of Metabolism?
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