Wang JS - Search Results

1

[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.

2

[Detection of enterovirus 71 and coxsackievirus A16 from children with hand, foot and mouth disease in Shanghai, 2002].

Yang ZH, Zhu QR, Li XZ, Wang XH, Wang JS, Hu JY, Tang W, Cui AL. Yang ZH, et al. Among authors: wang xh, wang js. Zhonghua Er Ke Za Zhi. 2005 Sep;43(9):648-52. Zhonghua Er Ke Za Zhi. 2005. PMID: 16191294 Chinese.

3

[Alagille syndrome in 5 Chinese children].

Wang JS, Wang XH, Wang ZL. Wang JS, et al. Among authors: wang xh, wang zl. Zhonghua Er Ke Za Zhi. 2007 Apr;45(4):308-9. Zhonghua Er Ke Za Zhi. 2007. PMID: 17706075 Chinese. No abstract available.

4

[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.

5

[SLC25A13 gene mutations in Chinese infants with intrahepatic cholestasis and abnormal blood amino acids].

Zhang SR, Wang JS, Wang XH, Zhu QR, Liu LY. Zhang SR, et al. Among authors: wang xh, wang js. Zhonghua Gan Zang Bing Za Zhi. 2008 Jun;16(6):445-8. Zhonghua Gan Zang Bing Za Zhi. 2008. PMID: 18578996 Chinese.

6

Clinical and pathological characteristics of Alagille syndrome in Chinese children.

Wang JS, Wang XH, Zhu QR, Wang ZL, Hu XQ, Zheng S. Wang JS, et al. Among authors: wang xh, wang zl. World J Pediatr. 2008 Nov;4(4):283-8. doi: 10.1007/s12519-008-0051-5. Epub 2008 Dec 23. World J Pediatr. 2008. PMID: 19104892

7

ABCB11 gene mutations in Chinese children with progressive intrahepatic cholestasis and low gamma glutamyltransferase.

Liu LY, Wang ZL, Wang XH, Zhu QR, Wang JS. Liu LY, et al. Among authors: wang xh, wang zl, wang js. Liver Int. 2010 Jul;30(6):809-15. doi: 10.1111/j.1478-3231.2009.02112.x. Epub 2009 Oct 21. Liver Int. 2010. PMID: 19845854

8

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

9

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

10

[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.

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