Jiang M - Search Results

1

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: jiang m. 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

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

[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. 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.

4

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

5

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

6

Detection of inborn errors of metabolism using GC-MS: over 3 years of experience in southern China.

Jiang M, Liu L, Mei H, Li X, Cheng J, Cai Y. Jiang M, et al. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):375-80. doi: 10.1515/jpem-2014-0164. J Pediatr Endocrinol Metab. 2015. PMID: 25781538

7

Combination of a Haploidentical Stem Cell Transplant With Umbilical Cord Blood for Cerebral X-Linked Adrenoleukodystrophy.

Jiang H, Jiang MY, Liu S, Cai YN, Liang CL, Liu L. Jiang H, et al. Pediatr Neurol. 2015 Aug;53(2):163-5.e1. doi: 10.1016/j.pediatrneurol.2015.05.002. Epub 2015 May 14. Pediatr Neurol. 2015. PMID: 26088837

8

Williams-Beuren Syndrome: A Case Confirmed by Array-CGH Method.

Jiang M, Liu L. Jiang M, et al. Iran J Pediatr. 2015 Feb;25(1):e247. doi: 10.5812/ijp.247. Epub 2015 Feb 21. Iran J Pediatr. 2015. PMID: 26199689 Free PMC article. No abstract available.

9

Clinical, biochemical, neuroimaging and molecular findings of X-linked Adrenoleukodystrophy patients in South China.

Jiang MY, Cai YN, Liang CL, Peng MZ, Sheng HY, Fan LP, Lin RZ, Jiang H, Huang Y, Liu L. Jiang MY, et al. Metab Brain Dis. 2015 Dec;30(6):1439-44. doi: 10.1007/s11011-015-9717-6. Epub 2015 Aug 12. Metab Brain Dis. 2015. PMID: 26260157

10

Brain abnormalities in fucosidosis: transplantation or supportive therapy?

Jiang M, Liu S, Jiang H, Lin Y, Shao Y, Hu H, Zhao X, Liu H, Huang Y, Liu L. Jiang M, et al. Among authors: jiang h. Metab Brain Dis. 2017 Apr;32(2):317-320. doi: 10.1007/s11011-017-9968-5. Epub 2017 Feb 25. Metab Brain Dis. 2017. PMID: 28238202

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