Jian She Wang

Summary

Affiliation: Fudan University
Country: China

Publications

  1. doi request reprint Zinc mono-therapy in pre-symptomatic Chinese children with Wilson disease: a single center, retrospective study
    Kuerbanjiang Abuduxikuer
    Liver Center, Children s Hospital of Fudan University, Shanghai, China
    PLoS ONE 9:e86168. 2014
  2. pmc Biochemical characteristics of neonatal cholestasis induced by citrin deficiency
    Jian She Wang
    Department of Pediatrics, Jinshan Hospital, Fudan University, Shanghai, China
    World J Gastroenterol 18:5601-7. 2012
  3. ncbi request reprint Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease in children
    Jian She Wang
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Minhang District, Shanghai, China
    World J Pediatr 6:148-53. 2010
  4. ncbi request reprint Transformation of hepatitis B serologic markers in babies born to hepatitis B surface antigen positive mothers
    Jian She Wang
    Laboratory of Infectious Diseases, Children s Hospital of Fudan University, 183 Fenglin Road, Shanghai 200032, China
    World J Gastroenterol 11:3582-5. 2005
  5. doi request reprint Clinical and pathological characteristics of Alagille syndrome in Chinese children
    Jian She Wang
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai, China
    World J Pediatr 4:283-8. 2008
  6. ncbi request reprint [Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection]
    Qi Rong Zhu
    Department of Infectious Disease, Children s Hospital, Fudan University, Shanghai 200032, China
    Zhonghua Liu Xing Bing Xue Za Zhi 26:236-9. 2005
  7. pmc Different regional distribution of SLC25A13 mutations in Chinese patients with neonatal intrahepatic cholestasis
    Rui Chen
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai 201102, China
    World J Gastroenterol 19:4545-51. 2013
  8. doi request reprint ABCB11 gene mutations in Chinese children with progressive intrahepatic cholestasis and low gamma glutamyltransferase
    Li yan Liu
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai, China
    Liver Int 30:809-15. 2010
  9. doi request reprint Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations
    Ling Juan Fang
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai, China
    J Pediatr Gastroenterol Nutr 55:150-6. 2012
  10. doi request reprint The mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and aminoacidemia
    Hai Yan Fu
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, 399 Wanyuan Road, Minhang District, Shanghai 201102, People s Republic of China
    J Gastroenterol 46:510-8. 2011

Collaborators

Detail Information

Publications25

  1. doi request reprint Zinc mono-therapy in pre-symptomatic Chinese children with Wilson disease: a single center, retrospective study
    Kuerbanjiang Abuduxikuer
    Liver Center, Children s Hospital of Fudan University, Shanghai, China
    PLoS ONE 9:e86168. 2014
    ..There is no official consensus regarding zinc therapy in pre-symptomatic children with Wilson Disease (WD); more data is needed...
  2. pmc Biochemical characteristics of neonatal cholestasis induced by citrin deficiency
    Jian She Wang
    Department of Pediatrics, Jinshan Hospital, Fudan University, Shanghai, China
    World J Gastroenterol 18:5601-7. 2012
    ..To explore differences in biochemical indices between neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) and that with other etiologies...
  3. ncbi request reprint Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease in children
    Jian She Wang
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Minhang District, Shanghai, China
    World J Pediatr 6:148-53. 2010
    ..This study aimed to investigate the feasibility of morning urinary copper/creatinine or copper/zinc ratio as replacement parameter for diagnosing Wilson's disease...
  4. ncbi request reprint Transformation of hepatitis B serologic markers in babies born to hepatitis B surface antigen positive mothers
    Jian She Wang
    Laboratory of Infectious Diseases, Children s Hospital of Fudan University, 183 Fenglin Road, Shanghai 200032, China
    World J Gastroenterol 11:3582-5. 2005
    ....
  5. doi request reprint Clinical and pathological characteristics of Alagille syndrome in Chinese children
    Jian She Wang
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai, China
    World J Pediatr 4:283-8. 2008
    ..This study was undertaken to investigate the significance of AS in Chinese children with chronic cholestasis and to describe its clinical and histological features...
  6. ncbi request reprint [Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection]
    Qi Rong Zhu
    Department of Infectious Disease, Children s Hospital, Fudan University, Shanghai 200032, China
    Zhonghua Liu Xing Bing Xue Za Zhi 26:236-9. 2005
    ....
  7. pmc Different regional distribution of SLC25A13 mutations in Chinese patients with neonatal intrahepatic cholestasis
    Rui Chen
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai 201102, China
    World J Gastroenterol 19:4545-51. 2013
    ..To investigate the differences in the mutation spectra of the SLC25A13 gene mutations from specific regions of China...
  8. doi request reprint ABCB11 gene mutations in Chinese children with progressive intrahepatic cholestasis and low gamma glutamyltransferase
    Li yan Liu
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai, China
    Liver Int 30:809-15. 2010
    ..ABCB11 gene mutations causing PFIC2 have been reported in some population groups, but not in mainland Chinese...
  9. doi request reprint Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations
    Ling Juan Fang
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai, China
    J Pediatr Gastroenterol Nutr 55:150-6. 2012
    ....
  10. doi request reprint The mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and aminoacidemia
    Hai Yan Fu
    The Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, 399 Wanyuan Road, Minhang District, Shanghai 201102, People s Republic of China
    J Gastroenterol 46:510-8. 2011
    ..The aim of this study was to explore the mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and various forms of aminoacidemia...
  11. doi request reprint Association of variants of ABCB11 with transient neonatal cholestasis
    Li yan Liu
    Department of Pediatrics, Center for Pediatric Liver Disease, Children s Hospital of Fudan University, Shanghai Medical College of Fudan University, Shanghai, China
    Pediatr Int 55:138-44. 2013
    ..The significance of ABCB11 variants have been studied in some cholestatic diseases, but this is not clear in transient neonatal cholestasis (TNC). The aim of the present study was to explore the association between ABCB11 variants and TNC...
  12. doi request reprint [Characteristics of the plasma amino acid spectrum of neonatal intrahepatic cholestasis caused by citrin deficiency]
    Hai Yan Fu
    Children s Hospital of Fudan University, Shanghai 201102, China
    Zhonghua Gan Zang Bing Za Zhi 21:934-9. 2013
    ..To investigate the plasma amino acid spectrum in infants more than 1-year-old with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in order to identify potential diagnostic markers of NICCD...
  13. pmc Primary ∆4-3-oxosteroid 5β-reductase deficiency: two cases in China
    Jing Zhao
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai 201102, China
    World J Gastroenterol 18:7113-7. 2012
    ..With ursodeoxycholic acid treatment and fat-soluble vitamin supplements, liver function tests normalized rapidly, and the degree of hepatomegaly was markedly reduced in both patients...
  14. ncbi request reprint [SLC25A13 gene mutations in Chinese infants with intrahepatic cholestasis and abnormal blood amino acids]
    Shao Ren Zhang
    Center for Pediatric Liver Diseases of Fudan University, Children s Hospital of Fudan University, Shanghai 200032, China
    Zhonghua Gan Zang Bing Za Zhi 16:445-8. 2008
    ..To explore whether SLC25A13 gene mutation exists and what is its mutation spectrum in mainland Chinese infants with intrahepatic cholestasis and abnormal blood amino acids...
  15. pmc Most common SLC25A13 mutation in 400 Chinese infants with intrahepatic cholestasis
    Hai Yan Fu
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, 399 Wanyuan Road, Minhang District, Shanghai 201102, China
    World J Gastroenterol 16:2278-82. 2010
    ..To establish the real time fluorescence polymerase chain reaction (RT-PCR) with dual labeled probes for fast detection of SLC25A13 gene mutation 851del4...
  16. pmc Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations
    Xin Hua Li
    Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China
    BMC Med Genet 12:6. 2011
    ..Wilson's disease (WND) is a rare autosomal recessive disorder. Here we have evaluated 62 WND cases (58 probands) from the Chinese Han population to expand our knowledge of ATP7B mutations and to more completely characterize WND in China...
  17. ncbi request reprint [Clinical features of hepatolenticular degeneration in children]
    Yi Lu
    Children s Hospital of Fudan University, Shanghai, China
    Zhonghua Gan Zang Bing Za Zhi 16:224-6. 2008
    ..To review the clinical features and liver pathology in children with hepatolenticular degeneration...
  18. doi request reprint Characterization of ATP8B1 gene mutations and a hot-linked mutation found in Chinese children with progressive intrahepatic cholestasis and low GGT
    Li yan Liu
    Center for Pediatric Liver Diseases, Children s Hospital of Fudan University Department of Pediatrics, Shanghai Medical College of Fudan University, 399 Wanyuan Road, Minhang, Shanghai, China
    J Pediatr Gastroenterol Nutr 50:179-83. 2010
    ..The aim of the study was to elucidate the role and characteristics of ATP8B1 gene mutations in mainland Chinese children with progressive intrahepatic cholestasis and low gamma-glutamyltransferase (GGT)...
  19. ncbi request reprint Two novel VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China
    Li Ting Li
    Li Ting Li, Jing Zhao, Rui Chen, Jian She Wang, Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai 201102, China
    World J Gastroenterol 20:326-9. 2014
    ..Genetic testing revealed two novel mutations (c.1033delA and c.1567C>T) in the VPS33B gene. The patient is a compound heterozygote and her parents were heterozygous for each of the mutations...
  20. ncbi request reprint Relationship between cytokines gene polymorphism and susceptibility to hepatitis B virus intrauterine infection
    Qi Rong Zhu
    Department of Infection Disease, Children s Hospital, Fudan University, Shanghai 200032, China
    Chin Med J (Engl) 118:1604-9. 2005
    ....
  21. ncbi request reprint [Interruption of the transmission of hepatitis B virus from mother to babies]
    Jian She Wang
    Department of Infectious Diseases, Children s Hospital of Fudan University, Shanghai 200032, China
    Zhonghua Gan Zang Bing Za Zhi 10:308-10. 2002
  22. ncbi request reprint ARC syndrome with high GGT cholestasis caused by VPS33B mutations
    Jian She Wang
    Jian She Wang, Jing Zhao, Li Ting Li, Center for Pediatric Liver Diseases, Children s Hospital of Fudan University, Shanghai 201102, China
    World J Gastroenterol 20:4830-4. 2014
    ..1509-1510insG. The mechanism of high GGT in this patient is unclear. Nevertheless, this case indicates that ARC syndrome cannot be excluded from the differential diagnosis of neonatal cholestasis even if high GGT activity is found...
  23. ncbi request reprint [Clinical characteristics of autoimmune hepatitis in 11 children]
    Yi Lu
    Department of Liver Diseases, Children s Hospital of Fudan University, Shanghai 201102, China
    Zhonghua Er Ke Za Zhi 48:758-63. 2010
    ..To investigate the clinical features of autoimmune hepatitis (AIH) in children so as to improve the awareness of the disease...
  24. ncbi request reprint A new frame-shifting mutation of UGT1A1 gene causes type I Crigler-Najjar syndrome
    Jin Wang
    Department of Neonatology, Children s Hospital of Fudan University, Shanghai 201102, China
    Chin Med J (Engl) 124:4109-11. 2011
    ..Both of his parents were heterozygous for the same mutation. A novel frame-shifting mutation of the UGT1A1 gene was found, confirming the diagnosis of Crigler-Najjar syndrome type I for this patient...
  25. ncbi request reprint [The 7th National Conference of Pediatric Hepatology was held in Chongqing]
    Jian She Wang
    Zhonghua Er Ke Za Zhi 42:247. 2004