Wang JS - Search Results

1

Infant cholestasis patient with a novel missense mutation in the AKR1D1 gene successfully treated by early adequate supplementation with chenodeoxycholic acid: A case report and review of the literature.

Wang HH, Wen FQ, Dai DL, Wang JS, Zhao J, Setchell KD, Shi LN, Zhou SM, Liu SX, Yang QH. Wang HH, et al. Among authors: wang js. World J Gastroenterol. 2018 Sep 21;24(35):4086-4092. doi: 10.3748/wjg.v24.i35.4086. World J Gastroenterol. 2018. PMID: 30254413 Free PMC article. Review.

2

Characterization of ATP8B1 gene mutations and a hot-linked mutation found in Chinese children with progressive intrahepatic cholestasis and low GGT.

Liu LY, Wang XH, Wang ZL, Zhu QR, Wang JS. Liu LY, et al. Among authors: wang xh, wang zl, wang js. J Pediatr Gastroenterol Nutr. 2010 Feb;50(2):179-83. doi: 10.1097/MPG.0b013e3181c1b368. J Pediatr Gastroenterol Nutr. 2010. PMID: 20038848

3

Most common SLC25A13 mutation in 400 Chinese infants with intrahepatic cholestasis.

Fu HY, Zhang SR, Yu H, Wang XH, Zhu QR, Wang JS. Fu HY, et al. Among authors: wang xh, wang js. World J Gastroenterol. 2010 May 14;16(18):2278-82. doi: 10.3748/wjg.v16.i18.2278. World J Gastroenterol. 2010. PMID: 20458766 Free PMC article.

4

The mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and aminoacidemia.

Fu HY, Zhang SR, Wang XH, Saheki T, Kobayashi K, Wang JS. Fu HY, et al. Among authors: wang xh, wang js. J Gastroenterol. 2011 Apr;46(4):510-8. doi: 10.1007/s00535-010-0329-y. Epub 2010 Oct 7. J Gastroenterol. 2011. PMID: 20927635

5

Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations.

Fang LJ, Wang XH, Knisely AS, Yu H, Lu Y, Liu LY, Wang JS. Fang LJ, et al. Among authors: wang xh, wang js. J Pediatr Gastroenterol Nutr. 2012 Aug;55(2):150-6. doi: 10.1097/MPG.0b013e31824ef36f. J Pediatr Gastroenterol Nutr. 2012. PMID: 22343912

6

Biochemical characteristics of neonatal cholestasis induced by citrin deficiency.

Wang JS, Wang XH, Zheng YJ, Fu HY, Chen R, Lu Y, Fang LJ, Saheki T, Kobayashi K. Wang JS, et al. Among authors: wang xh. World J Gastroenterol. 2012 Oct 21;18(39):5601-7. doi: 10.3748/wjg.v18.i39.5601. World J Gastroenterol. 2012. PMID: 23112554 Free PMC article.

7

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

Zhao J, Fang LJ, Setchell KD, Chen R, Li LT, Wang JS. Zhao J, et al. Among authors: wang js. World J Gastroenterol. 2012 Dec 21;18(47):7113-7. doi: 10.3748/wjg.v18.i47.7113. World J Gastroenterol. 2012. PMID: 23323017 Free PMC article.

8

Different regional distribution of SLC25A13 mutations in Chinese patients with neonatal intrahepatic cholestasis.

Chen R, Wang XH, Fu HY, Zhang SR, Abudouxikuer K, Saheki T, Wang JS. Chen R, et al. Among authors: wang xh, wang js. World J Gastroenterol. 2013 Jul 28;19(28):4545-51. doi: 10.3748/wjg.v19.i28.4545. World J Gastroenterol. 2013. PMID: 23901231 Free PMC article.

9

[Mutation analysis of FAH gene in patients with tyrosinemia type 1].

Dou LM, Fang LJ, Wang XH, Lu W, Chen R, Li LT, Zhao J, Wang JS. Dou LM, et al. Among authors: wang xh, wang js. Zhonghua Er Ke Za Zhi. 2013 Apr;51(4):302-7. Zhonghua Er Ke Za Zhi. 2013. PMID: 23927806 Chinese.

10

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

Li LT, Zhao J, Chen R, Wang JS. Li LT, et al. Among authors: wang js. World J Gastroenterol. 2014 Jan 7;20(1):326-9. doi: 10.3748/wjg.v20.i1.326. World J Gastroenterol. 2014. PMID: 24415890 Free PMC article.

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