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List of works by Jian-She Wang

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

scientific article

A fatal case of mitochondrial DNA depletion syndrome with novel compound heterozygous variants in the deoxyguanosine kinase gene.

scientific article published on 15 September 2017

A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report.

scientific article published on 25 June 2018

ARC syndrome with high GGT cholestasis caused by VPS33B mutations

scientific article published on April 2014

An international fellowship training program in pediatric emergency medicine: establishing a new subspecialty in the Land of the Dragon.

scientific article published on December 2011

Anemia following zinc treatment for Wilson's disease: a case report and literature review

scientific article published on 09 July 2019

Citrin deficiency presenting as acute liver failure in an eight-month-old infant.

scientific article published on June 2015

Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations.

scientific article

Effect of delivery mode on maternal-infant transmission of hepatitis B virus by immunoprophylaxis.

scientific article published in October 2002

Hypothyroidism Associated with ATP8B1 Deficiency.

scientific article published on 14 September 2015

Infection of the fetus with hepatitis B e antigen via the placenta

scientific article published on 01 March 2000

JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome

scientific article published on 15 June 2015

Low-GGT intrahepatic cholestasis associated with biallelic USP53 variants: Clinical, histological and ultrastructural characterization

scientific article published on 02 March 2020

Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature.

scientific article

Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective study

scientific article

Novel methionyl-tRNA synthetase gene variants/phenotypes in interstitial lung and liver disease: A case report and review of literature

article

Novel missense mutation in VPS33B is associated with isolated low gamma-glutamyltransferase cholestasis: Attenuated, incomplete phenotype of arthrogryposis, renal dysfunction, and cholestasis syndrome

scientific article published on 03 September 2019

Personal experience in pediatric emergency medicine training in Canada and China.

scientific article

Primary ∆4-3-oxosteroid 5β-reductase deficiency: two cases in China

scientific article

RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities

scientific article published on 13 June 2019

Recurrent acute liver failure associated with novel mutation: A case report

scientific article published on 01 February 2019

Significance of low or normal serum gamma glutamyl transferase level in infants with idiopathic neonatal hepatitis.

scientific article published on 13 June 2006

TJP2 hepatobiliary disorders: Novel variants and clinical diversity

scientific article published on 07 November 2019

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 response

article

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency

scientific article

Transformation of hepatitis B serologic markers in babies born to hepatitis B surface antigen positive mothers

scientific article

Two novel VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China.

scientific article published on January 2014

UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation

article

Zinc mono-therapy in pre-symptomatic Chinese children with Wilson disease: a single center, retrospective study

scientific article published on 24 January 2014

[An infant with persistent jaundice for 6 months: diagnosis and differential diagnosis of chronic infantile cholestasis]

scientific article published on 01 September 2011

[Clinical and laboratory characteristics of MEGDHEL syndrome in liver disease phenotype due to SERAC1 gene mutation]

scientific article published on 01 December 2018

[Focus on diagnosis and treatment of genetic liver disorders]

scientific article published on 01 December 2018

[Inherited metabolic diseases and liver transplantation]

scientific article published on 01 March 2019

[Interruption of the transmission of hepatitis B virus from mother to babies]

scientific article published on 01 August 2002

[Neonatal sclerosing cholangitis caused by DCDC2 variations in two siblings and literature review]

scientific article published on 01 August 2018

[Non-transplant surgical intervention in progressive familial intrahepatic cholestasis]

scientific article published on 01 May 2018

[Progressive familial intrahepatic cholestasis type 3]

scientific article published on 01 March 2010

[Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection]

scientific article published on 01 April 2005

[Relationship between phenotype and genotype of ABCB11 deficiency in siblings and literature review]

scientific article published on 01 June 2018

[Study on the S region gene mutation of hepatitis B virus during prevention of HBV transmission in uterus with hepatitis B immunoglobulin]

scientific article published on 01 June 2006

[The 7th National Conference of Pediatric Hepatology was held in Chongqing]

scientific article published on 01 April 2004

Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomes

article

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