Journal Updates


Microbiome Signatures Associated with Steatohepatitis and Moderate to Severe Fibrosis in Children With Nonalcoholic Fatty...
Measles, mumps, rubella (vaccine) and varicella vaccines in pediatric liver transplant: An initial analysis of post-...
Ledipasvir-Sofosbuvir for 12 Weeks in Children 3 to <6 Years Old With Chronic Hepatitis C.
Healthcare transition in pediatric liver transplantation: The perspectives of pediatric and adult healthcare professionals
Contribution of a genetic risk score to clinical prediction of hepatic steatosis in obese childrenand adolescents
Liver Ultrasound Patterns in Children with Cystic Fibrosis Correlate with Non-Invasive Tests of Liver Disease.
Gene Expression Signatures Associated With Survival Times of Pediatric Patients With Biliary Atresia Identify Potential...
Glycogen storage disease presenting as Cushing syndrome
Epstein-Barr virus infection with acute acalculous cholecystitis in previously healthy children


Non-alcoholic fatty liver infiltration in children: an underdiagnosed evolving disease
NRAS and KRAS polymorphisms are not associated with hepatoblastoma susceptibility in Chinese children.
Association Between Vitamin D Deficiency and Suspected Nonalcoholic Fatty Liver Disease in an Adolescent Population.
Psychotropic Medications are Associated with Increased Liver Disease Severity in Pediatric NAFLD.
Nonalcoholic fatty liver disease is associated with lower hepatitis B viral load and antiviral response in pediatric...
Risk Factors for Postoperative Prolonged Mechanical Ventilation After Pediatric LiverTransplantation.
Efficacy of dietary intervention and physical activity in children and adolescents with nonalcoholic fatty liver disease...
Liver Biochemical Abnormalities in Adolescent Patients with Turner Syndrome
Evaluation of the diagnostic biopsy approach for children with hepatoblastoma: A report from the Children's Oncology...


Clinical and biochemical footprints of inherited metabolic diseases. II. Metabolic liver diseases
Niemann-Pick disease type C caused by NPC1 mutation in a case
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