Wang Y - Search Results

1

[Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China].

Ye J, Qiu WJ, Han LS, Zhang HW, Zhou JD, Gao XL, Wang Y, Gu XF. Ye J, et al. Among authors: wang y. Zhonghua Er Ke Za Zhi. 2008 Apr;46(4):281-5. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099731 Chinese.

2

[Application of tandem mass spectrometry on the diagnosis of fatty acid oxidation disorders].

Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Zhang YJ, Gu XF. Han LS, et al. Among authors: wang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Dec;24(6):692-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 18067086 Chinese.

3

[Values of tandem mass spectrometry in etiologic diagnosis of cerebral developmental retardation].

Zhang JM, Gu XF, Shao XH, Song XQ, Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Wang MX. Zhang JM, et al. Among authors: wang mx, wang y. Zhonghua Er Ke Za Zhi. 2007 Dec;45(12):932-6. Zhonghua Er Ke Za Zhi. 2007. PMID: 18339284 Chinese.

4

[Diagnosis of inborn errors of metabolism using tandem mass spectrometry and gas chromatography mass spectrometry].

Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Jin J, Gu XF. Han LS, et al. Among authors: wang y. Zhonghua Yi Xue Za Zhi. 2008 Aug 5;88(30):2122-6. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19080473 Chinese.

5

[Clinical and mutational study of a Chinese infant with isovaleric acidemia].

Qiu WJ, Gu XF, Ye J, Han LS, Bai HT, Wang X, Gao XL, Wang Y, Jin J, Zhang HW. Qiu WJ, et al. Among authors: wang x, wang y. Zhonghua Er Ke Za Zhi. 2008 Jul;46(7):526-30. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099814 Chinese.

6

[Enzymatic diagnosis of 47 cases with mucopolysaccharidosis].

Zhang HW, Wang Y, Ye J, Qiu WJ, Han LS, Gao XL, Gu XF. Zhang HW, et al. Among authors: wang y. Zhonghua Er Ke Za Zhi. 2009 Apr;47(4):276-80. Zhonghua Er Ke Za Zhi. 2009. PMID: 19555566 Chinese.

7

[Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia].

Wang F, Han LS, Hu YH, Yang YL, Ye J, Qiu WJ, Zhang YF, Gao XL, Wang Y, Gu XF. Wang F, et al. Among authors: wang y. Zhonghua Er Ke Za Zhi. 2009 Mar;47(3):189-93. Zhonghua Er Ke Za Zhi. 2009. PMID: 19573432 Chinese.

8

[Diagnosis, treatment and gene mutation analysis in children with holocarboxylase synthetas deficiency].

Wang T, Ye J, Han LS, Qiu WJ, Zhang HW, Zhang YF, Gao XL, Wang Y, Gu XF. Wang T, et al. Among authors: wang y. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Aug;11(8):609-12. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19695181 Free article. Chinese.

9

[Analysis of the MUT gene mutations in patients with methylmalonic acidemia].

Wang F, Han L, Ye J, Qiu W, Zhang Y, Gao X, Wang Y, Yang Y, Gu X. Wang F, et al. Among authors: wang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):485-9. doi: 10.3760/cma.j.issn.1003-9406.2009.05.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806564 Chinese.

10

[Gene mutation analyses in Chinese children with multiple carboxylase deficiency].

Wang T, Ye J, Han LS, Qiu WJ, Zhang HW, Zhang YF, Gao XL, Wang Y, Gu XF. Wang T, et al. Among authors: wang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):504-10. doi: 10.3760/cma.j.issn.1003-9406.2009.05.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806568 Chinese.

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