Liu L - Search Results

1

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: liu l. Gene. 2013 Dec 10;532(1):46-52. doi: 10.1016/j.gene.2013.08.097. Epub 2013 Sep 11. Gene. 2013. PMID: 24035930

2

[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. Among authors: liu l. 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.

3

[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. Among authors: liu l, liu hs. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):601-5. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158738 Chinese.

4

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: liu l. 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

5

[Gene mutations and clinical manifestations in children with glycogen storage disease type Ib].

Liang CL, Liu L, Sheng HY, Jiang MY, Yin X, Mei HF, Cheng J, Zhang W, Fan LP. Liang CL, et al. Among authors: liu l. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Aug;15(8):661-5. Zhongguo Dang Dai Er Ke Za Zhi. 2013. PMID: 23965881 Free article. Chinese.

6

Separation and identification of underivatized plasma acylcarnitine isomers using liquid chromatography-tandem mass spectrometry for the differential diagnosis of organic acidemias and fatty acid oxidation defects.

Peng M, Fang X, Huang Y, Cai Y, Liang C, Lin R, Liu L. Peng M, et al. Among authors: liu l. J Chromatogr A. 2013 Dec 6;1319:97-106. doi: 10.1016/j.chroma.2013.10.036. Epub 2013 Oct 16. J Chromatogr A. 2013. PMID: 24169039

7

[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: liu h, liu l. Zhonghua Er Ke Za Zhi. 2014 Apr;52(4):313-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 24915922 Chinese.

8

[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: liu l. Zhonghua Er Ke Za Zhi. 2014 Jun;52(6):403-8. Zhonghua Er Ke Za Zhi. 2014. PMID: 25190157 Chinese.

9

A novel ABCD1 gene mutation in a Chinese patient with X-linked adrenoleukodystrophy.

Cai YN, Jiang MY, Liang CL, Peng MZ, Cheng J, Sheng HY, Fan LP, Chen XQ, Liu L. Cai YN, et al. Among authors: liu l. J Pediatr Endocrinol Metab. 2015 May;28(5-6):725-9. doi: 10.1515/jpem-2013-0441. J Pediatr Endocrinol Metab. 2015. PMID: 25423669

10

First case report of medium-chain acyl-coenzyme A dehydrogenase deficiency in China.

Liang C, Jiang M, Sheng H, Cai Y, Wu D, Yin X, Peng M, Liu L. Liang C, et al. Among authors: liu l. J Pediatr Endocrinol Metab. 2015 May;28(5-6):681-4. doi: 10.1515/jpem-2014-0058. J Pediatr Endocrinol Metab. 2015. PMID: 25503862

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