Ye J - Search Results

1

Phenylalanine Hydroxylase Deficiency and Citrin Deficiency in a Chinese Infant.

Ye J, Qiu WJ, Han LS, Zhang HW, Gu XF. Ye J, et al. Chin Med J (Engl). 2015 Nov 5;128(21):2979-80. doi: 10.4103/0366-6999.168084. Chin Med J (Engl). 2015. PMID: 26521805 Free PMC article. No abstract available.

2

[Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test].

Zhang ZX, Ye J, Qiu WJ, Han LS, Gu XF. Zhang ZX, et al. Among authors: ye j. Zhonghua Er Ke Za Zhi. 2005 May;43(5):335-9. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924746 Chinese.

3

[Clinical study of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency in southern and northern Chinese patients].

Yang L, Zhang ZX, Ye J, Zhou ZS, Shen M, Han LS, Qiu W, Yu WM, Gu XF. Yang L, et al. Among authors: ye j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Jun;24(3):310-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17557244 Chinese.

4

[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. Zhonghua Er Ke Za Zhi. 2008 Apr;46(4):281-5. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099731 Chinese.

5

[The investigation of differential diagnostic development and incidence of tetrahydrobiopterin deficiency].

Ye J, Qiu WJ, Han LS, Zhou JD, Gao XL, Gu XF. Ye J, et al. Zhonghua Yu Fang Yi Xue Za Zhi. 2009 Feb;43(2):128-31. Zhonghua Yu Fang Yi Xue Za Zhi. 2009. PMID: 19534905 Chinese.

6

[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: ye j. 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.

7

[Studies on the clinical manifestation and SLC25A13 gene mutation of Chinese patients with neonatal intrahepatic cholestasis caused by citrin deficiency].

Xing YZ, Qiu WJ, Ye J, Han LS, Xu SS, Zhang HW, Gao XL, Wang Y, Gu XF. Xing YZ, et al. Among authors: ye j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Apr;27(2):180-5. doi: 10.3760/cma.j.issn.1003-9406.2010.02.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20376801 Chinese.

8

[Primary carnitine deficiency in 17 patients: diagnosis, treatment and follow up].

Han LS, Ye J, Qiu WJ, Zhang HW, Wang Y, Ji WJ, Gao XL, Li XY, Jin J, Gu XF. Han LS, et al. Among authors: ye j. Zhonghua Er Ke Za Zhi. 2012 Jun;50(6):405-9. Zhonghua Er Ke Za Zhi. 2012. PMID: 22931933 Chinese.

9

Variations in genotype-phenotype correlations in phenylalanine hydroxylase deficiency in Chinese Han population.

Zhu T, Ye J, Han L, Qiu W, Zhang H, Liang L, Gu X. Zhu T, et al. Among authors: ye j. Gene. 2013 Oct 15;529(1):80-7. doi: 10.1016/j.gene.2013.07.079. Epub 2013 Aug 7. Gene. 2013. PMID: 23932990

10

[Tyrosine hydroxylase deficiency: a case of autosomal recessive dopa-responsive dystonia].

Tan D, Zhang Y, Ye J, Han L, Qiu W, Gu X, Zhang H. Tan D, et al. Among authors: ye j. Zhonghua Er Ke Za Zhi. 2014 Aug;52(8):616-9. Zhonghua Er Ke Za Zhi. 2014. PMID: 25224241 Chinese.

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