about
Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations.Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective studyTransformation of hepatitis B serologic markers in babies born to hepatitis B surface antigen positive mothersJAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome.Citrin deficiency presenting as acute liver failure in an eight-month-old infant.The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.Primary ∆4-3-oxosteroid 5β-reductase deficiency: two cases in ChinaSignificance of low or normal serum gamma glutamyl transferase level in infants with idiopathic neonatal hepatitis.Two novel VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China.Zinc mono-therapy in pre-symptomatic Chinese children with Wilson disease: a single center, retrospective study.ARC syndrome with high GGT cholestasis caused by VPS33B mutations.Hypothyroidism Associated with ATP8B1 Deficiency.A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions.An international fellowship training program in pediatric emergency medicine: establishing a new subspecialty in the Land of the Dragon.Effect of delivery mode on maternal-infant transmission of hepatitis B virus by immunoprophylaxis.A fatal case of mitochondrial DNA depletion syndrome with novel compound heterozygous variants in the deoxyguanosine kinase gene.Personal experience in pediatric emergency medicine training in Canada and China.A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report.Novel methionyl-tRNA synthetase gene variants/phenotypes in interstitial lung and liver disease: A case report and review of literature[Neonatal sclerosing cholangitis caused by DCDC2 variations in two siblings and literature review][Relationship between phenotype and genotype of ABCB11 deficiency in siblings and literature review]Tandem mass spectrometric determination of atypical 3β-hydroxy-Δ5-bile acids in patients with 3β-hydroxy-Δ5-C27-steroid oxidoreductase deficiency: application to diagnosis and monitoring of bile acid therapeutic responseUGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlationRecurrent acute liver failure associated with novel mutation: A case reportΔ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomesNovel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature.Infection of the fetus with hepatitis B e antigen via the placenta[Interruption of the transmission of hepatitis B virus from mother to babies][Study on the S region gene mutation of hepatitis B virus during prevention of HBV transmission in uterus with hepatitis B immunoglobulin][The 7th National Conference of Pediatric Hepatology was held in Chongqing][Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection][An infant with persistent jaundice for 6 months: diagnosis and differential diagnosis of chronic infantile cholestasis][Progressive familial intrahepatic cholestasis type 3][Non-transplant surgical intervention in progressive familial intrahepatic cholestasis]Low-GGT intrahepatic cholestasis associated with biallelic USP53 variants: Clinical, histological and ultrastructural characterizationTJP2 hepatobiliary disorders: Novel variants and clinical diversity[Focus on diagnosis and treatment of genetic liver disorders][Clinical and laboratory characteristics of MEGDHEL syndrome in liver disease phenotype due to SERAC1 gene mutation]Anemia following zinc treatment for Wilson's disease: a case report and literature review[Inherited metabolic diseases and liver transplantation]
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jian-She Wang
@ast
Jian-She Wang
@en
Jian-She Wang
@es
Jian-She Wang
@nl
type
label
Jian-She Wang
@ast
Jian-She Wang
@en
Jian-She Wang
@es
Jian-She Wang
@nl
prefLabel
Jian-She Wang
@ast
Jian-She Wang
@en
Jian-She Wang
@es
Jian-She Wang
@nl
P106
P1153
55742657600
P31
P496
0000-0003-0823-586X