Zhao X - Search Results

1

Clinical and molecular characteristics of 11 Chinese probands with GM1 gangliosidosis.

Feng Y, Huang Y, Zhao X, Sheng H, Feng Y, Zhang W, Liu L. Feng Y, et al. Among authors: zhao x. Metab Brain Dis. 2018 Dec;33(6):2051-2057. doi: 10.1007/s11011-018-0315-2. Epub 2018 Sep 28. Metab Brain Dis. 2018. PMID: 30267299

2

[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.

3

[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.

4

[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.

5

[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.

6

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

7

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

8

[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.

9

[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.

10

[Maturity-onset diabetes of the young 2 with a novel mutation of glucokinase gene in a Chinese boy and the clinical follow-up].

Li X, Liu L, Liang C, Sheng H, Zhao X. Li X, et al. Among authors: zhao x. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):867-71. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582477 Chinese.

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