Yuan-yuan Kong
Beijing, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications
Fluctuations and Determinants of Amino Acids and Acylcarnitine Species in Newborn Screening by Tandem Mass Spectrometry.
Journal: Fetal and pediatric pathology
Published: July 08, 2026
Expert consensus on the combined screening of genes and biomarkers for neonatal diseases.
Journal: World journal of pediatrics : WJP
Published: July 07, 2025
Multiple Low-Level Viraemia Suggest Hindered Liver Fibrosis Regression in Chronic Hepatitis B Patients During Antiviral Therapy.
Journal: Journal of viral hepatitis
Published: March 26, 2024
Prognostic Factors Related to In-hospital Death in Children with Biliary Atresia: Analysis of a Nationwide Inpatient Database.
Journal: Journal of clinical and translational hepatology
Published: October 11, 2021
Repeatability and Reliability of Home-Based Stool Color Card Screening for Biliary Atresia Based on Results in China and Japan.
Journal: The Tohoku journal of experimental medicine
Published: December 21, 2020
Liver Transplantation for Propionic Acidemia: Evidence From a Systematic Review and Meta-analysis.
Journal: Transplantation
Published: October 23, 2020
Factors influencing in-hospital death for pediatric patients with isolated methylmalonic acidemia: a nationwide inpatient database analysis.
Journal: Orphanet journal of rare diseases
Published: February 20, 2020
Inborn errors of metabolism detectable by tandem mass spectrometry in Beijing.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: September 10, 2019
Methylmalonic and propionic acidemia among hospitalized pediatric patients: a nationwide report.
Journal: Orphanet journal of rare diseases
Published: September 05, 2019
Histologic pattern is better correlated with clinical outcomes than biochemical classification in patients with drug-induced liver injury.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: March 31, 2019
Whole-exome sequencing as a powerful tool for identifying genetic causes in a patient with POLG-related disorders and phenylketonuria.
Journal: The Journal of international medical research
Published: January 26, 2019
Last Updated: 09/26/2026