Zhao X - Search Results

1

Clinical and GAA gene mutation analysis in 21 Chinese patients with classic infantile pompe disease.

Su X, Sheng H, Huang Y, Li X, Zhang W, Zhao X, Li C, Liu L. Su X, et al. Among authors: zhao x. Eur J Med Genet. 2020 Dec;63(12):103997. doi: 10.1016/j.ejmg.2020.103997. Epub 2020 Jul 22. Eur J Med Genet. 2020. PMID: 32711049

2

A novel mutation of estrogen receptor gene detected in girls with precocious puberty.

Li B, Liu L, Fu X, Zhou WQ, Zou DT, Zhao XY, Cai YN, Tu HB, Liu QC, Chen YY. Li B, et al. Among authors: zhao xy. Yi Chuan Xue Bao. 2005 Oct;32(10):1011-7. Yi Chuan Xue Bao. 2005. PMID: 16252695

3

[Gene mutation analysis in four Chinese patients with multiple carboxylase deficiency].

Li D, Liu L, Li XZ, Cheng J, Zhao XY, Zhou R. Li D, et al. Zhonghua Er Ke Za Zhi. 2006 Nov;44(11):865-8. Zhonghua Er Ke Za Zhi. 2006. PMID: 17274881 Chinese.

4

[Mucopolysaccharidosis VII: report of a case and review of the literature].

Huang YL, Li SY, Zhao XY, Liu HS, Ou XB, Liu L. Huang YL, et al. Zhonghua Er Ke Za Zhi. 2011 Jun;49(6):455-8. Zhonghua Er Ke Za Zhi. 2011. PMID: 21924061 Review. Chinese.

5

[Enzymatic diagnosis and clinical characteristics of 52 children with mucopolysaccharidosis].

Huang YL, Li SY, Zhao XY, Fan LP, Lin WC, Zhou ZH, Cheng J, Liu L. Huang YL, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Jul;14(7):510-4. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22809603 Free article. Chinese.

6

[Wolman disease with novel mutation of LIPA gene in a Chinese infant].

Huang YL, Sheng HY, Zhao XY, Yu JK, Li L, Liu HS, Gu CM, He DM, Liu L. Huang YL, et al. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):601-5. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158738 Chinese.

7

Measurement of free carnitine and acylcarnitines in plasma by HILIC-ESI-MS/MS without derivatization.

Peng M, Liu L, Jiang M, Liang C, Zhao X, Cai Y, Sheng H, Ou Z, Luo H. Peng M, et al. Among authors: zhao x. J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Aug 1;932:12-8. doi: 10.1016/j.jchromb.2013.05.028. Epub 2013 Jun 2. J Chromatogr B Analyt Technol Biomed Life Sci. 2013. PMID: 23816563

8

Molecular genetic assay of mucopolysaccharidosis IVA in South China.

He D, Huang Y, Ou Z, Sheng H, Li S, Zhao X, Li R, Zheng J, Liu L. He D, et al. Among authors: zhao x. Gene. 2013 Dec 10;532(1):46-52. doi: 10.1016/j.gene.2013.08.097. Epub 2013 Sep 11. Gene. 2013. PMID: 24035930

9

[Clinical and molecular characteristics of a child with juvenile Sandhoff disease].

Huang Y, Xie T, Zheng J, Zhao X, Liu H, Liu L. Huang Y, et al. Among authors: zhao x. Zhonghua Er Ke Za Zhi. 2014 Apr;52(4):313-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 24915922 Chinese.

10

[Analysis of clinical features and arylsulfatase B gene mutation in thirteen Chinese children with mucopolysaccharidosis type VI].

Zheng J, Huang Y, Zhao X, Sheng H, Cheng J, Zhou Z, Li X, Mao X, Liu L. Zheng J, et al. Among authors: zhao x. Zhonghua Er Ke Za Zhi. 2014 Jun;52(6):403-8. Zhonghua Er Ke Za Zhi. 2014. PMID: 25190157 Chinese.

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