Sheng HY - Search Results

1

Simultaneous quantification of 48 plasma amino acids by liquid chromatography-tandem mass spectrometry to investigate urea cycle disorders.

Peng MZ, Cai YN, Shao YX, Zhao L, Jiang MY, Lin YT, Yin X, Sheng HY, Liu L. Peng MZ, et al. Among authors: sheng hy. Clin Chim Acta. 2019 Aug;495:406-416. doi: 10.1016/j.cca.2019.05.011. Epub 2019 May 13. Clin Chim Acta. 2019. PMID: 31095934

2

First case report of short-chain acyl-CoA dehydrogenase deficiency in China.

Jiang M, Liu L, Peng M, Liang C, Sheng H, Cai Y. Jiang M, et al. J Pediatr Endocrinol Metab. 2012;25(7-8):795-7. doi: 10.1515/jpem-2012-0185. J Pediatr Endocrinol Metab. 2012. PMID: 23155713 Free article.

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: sheng hy. 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. 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: sheng hy. 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

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

7

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

8

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: sheng hy. J Pediatr Endocrinol Metab. 2015 May;28(5-6):725-9. doi: 10.1515/jpem-2013-0441. J Pediatr Endocrinol Metab. 2015. PMID: 25423669

9

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. J Pediatr Endocrinol Metab. 2015 May;28(5-6):681-4. doi: 10.1515/jpem-2014-0058. J Pediatr Endocrinol Metab. 2015. PMID: 25503862

10

[Clinical features of pyruvate dehydrogenase complex deficiency and gene testing in one case].

Wu M, Liu L, Cai Y, Sheng H, Cheng J, Li X, Yin X, Lu Z, Lin R, Zhou Z, Fan L, Liu H. Wu M, et al. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):863-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582476 Chinese.

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