Jiang M - Search Results

1

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

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

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

4

[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.

5

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

6

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.

7

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

8

Clinical and mutation analysis of 24 Chinese patients with ornithine transcarbamylase deficiency.

Shao Y, Jiang M, Lin Y, Mei H, Zhang W, Cai Y, Su X, Hu H, Li X, Liu L. Shao Y, et al. Among authors: jiang m. Clin Genet. 2017 Sep;92(3):318-322. doi: 10.1111/cge.13004. Epub 2017 Mar 30. Clin Genet. 2017. PMID: 28266016

9

Early transition from insulin to sulfonylureas in neonatal diabetes and follow-up: Experience from China.

Li X, Xu A, Sheng H, Ting TH, Mao X, Huang X, Jiang M, Cheng J, Liu L. Li X, et al. Among authors: jiang m. Pediatr Diabetes. 2018 Mar;19(2):251-258. doi: 10.1111/pedi.12560. Epub 2017 Aug 8. Pediatr Diabetes. 2018. PMID: 28791793

10

Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY).

Li X, Ting TH, Sheng H, Liang CL, Shao Y, Jiang M, Xu A, Lin Y, Liu L. Li X, et al. Among authors: jiang m. BMC Pediatr. 2018 Mar 6;18(1):101. doi: 10.1186/s12887-018-1060-8. BMC Pediatr. 2018. PMID: 29510678 Free PMC article.

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