Wang JS - Search Results

1

Wilson disease with hepatic presentation in an eight-month-old boy.

Abuduxikuer K, Li LT, Qiu YL, Wang NL, Wang JS. Abuduxikuer K, et al. Among authors: wang nl, wang js. World J Gastroenterol. 2015 Aug 7;21(29):8981-4. doi: 10.3748/wjg.v21.i29.8981. World J Gastroenterol. 2015. PMID: 26269689 Free PMC article.

2

[Clinical features of hepatolenticular degeneration in children].

Lu Y, Wang XH, Wang JS. Lu Y, et al. Among authors: wang xh, wang js. Zhonghua Gan Zang Bing Za Zhi. 2008 Mar;16(3):224-6. Zhonghua Gan Zang Bing Za Zhi. 2008. PMID: 18364085 Chinese.

3

Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease in children.

Wang JS, Lu Y, Wang XH, Zhu QR. Wang JS, et al. Among authors: wang xh. World J Pediatr. 2010 May;6(2):148-53. doi: 10.1007/s12519-010-0023-4. Epub 2010 Feb 1. World J Pediatr. 2010. PMID: 20127216

4

[The reassessment of the diagnostic value of 24-hour urinary copper excretion in children with Wilson's disease].

Lu Y, Liu XQ, Wang XH, Wang JS. Lu Y, et al. Among authors: wang xh, wang js. Zhonghua Gan Zang Bing Za Zhi. 2010 Jan;18(1):49-53. doi: 10.3760/cma.j.issn.1007-3418.2010.01.012. Zhonghua Gan Zang Bing Za Zhi. 2010. PMID: 20128970 Chinese.

5

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.

6

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

Li XH, Lu Y, Ling Y, Fu QC, Xu J, Zang GQ, Zhou F, De-Min Y, Han Y, Zhang DH, Gong QM, Lu ZM, Kong XF, Wang JS, Zhang XX. Li XH, et al. Among authors: wang js. BMC Med Genet. 2011 Jan 11;12:6. doi: 10.1186/1471-2350-12-6. BMC Med Genet. 2011. PMID: 21219664 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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