Jiang YW - Search Results

1

[Clinical follow-up study of myelin oligodendrocyte glycoprotein antibody-associated disease in children].

Teng XL, Zhang J, Chang XT, Li SR, Zhou J, Zhang YH, Bao XH, Jiang YW, Wu Y. Teng XL, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2021 Dec 2;59(12):1048-1054. doi: 10.3760/cma.j.cn112140-20210703-00549. Zhonghua Er Ke Za Zhi. 2021. PMID: 34856664 Chinese.

2

Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.

Zhang Y, Yang YL, Sun F, Cai X, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Zhang YH, Jiang YW, Qin J, Wu XR. Zhang Y, et al. Among authors: jiang yw. J Inherit Metab Dis. 2007 Apr;30(2):265. doi: 10.1007/s10545-006-0481-y. Epub 2007 Feb 24. J Inherit Metab Dis. 2007. PMID: 17323145

3

[Genotype and phenotype of female Dravet syndrome with PCDH19 mutations].

Liu AJ, Zhang YH, Xu XJ, Yang XL, Yang ZX, Wu Y, Liu XY, Jiang YW, Wu XR. Liu AJ, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2016 May;54(5):327-31. doi: 10.3760/cma.j.issn.0578-1310.2016.05.004. Zhonghua Er Ke Za Zhi. 2016. PMID: 27143072 Chinese.

4

[Clinical and genetic characteristics and detection of urinary pipecolic acid in pyridoxine dependent epilepsy].

Xue J, Yang ZX, Li H, Qian P, Wu Y, Jiang YW, Liu XY. Xue J, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2016 Aug;54(8):592-6. doi: 10.3760/cma.j.issn.0578-1310.2016.08.007. Zhonghua Er Ke Za Zhi. 2016. PMID: 27510871 Chinese.

5

[Clinical features and gene mutations in epilepsy of infancy with migrating focal seizures].

Shang KW, Zhang YH, Yang XL, Liu AJ, Yang ZX, Liu XY, Jiang YW, Wu XR. Shang KW, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2016 Oct 2;54(10):735-739. doi: 10.3760/cma.j.issn.0578-1310.2016.10.005. Zhonghua Er Ke Za Zhi. 2016. PMID: 27784474 Chinese.

6

[Clinical and neuroimaging features of acute encephalopathy after status epilepticus in Dravet syndrome].

Tian XJ, Zhang YH, Liu AJ, Yang XL, Zeng Q, Yang ZX, Ye JT, Liu XY, Jiang YW, Wu XR. Tian XJ, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):277-282. doi: 10.3760/cma.j.issn.0578-1310.2017.04.009. Zhonghua Er Ke Za Zhi. 2017. PMID: 28441824 Chinese.

7

[Follow-up and genetic study of 43 Chinese children with type Ⅰ Alexander disease].

Ban TT, Wu Y, Zhang ZB, Zang LL, Wang JM, Jiang YW. Ban TT, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2017 Jul 2;55(7):504-508. doi: 10.3760/cma.j.issn.0578-1310.2017.07.007. Zhonghua Er Ke Za Zhi. 2017. PMID: 28728258 Chinese.

8

[Phenotypic and genotypic features of twenty children with classic pantothenate kinase-associated neurodegeneration].

Zhou J, He J, Kou LP, Feng HC, Deng YH, Zhang ZB, Zhou L, Wang JM, Jiang YW, Wu Y. Zhou J, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2017 Sep 2;55(9):678-682. doi: 10.3760/cma.j.issn.0578-1310.2017.09.011. Zhonghua Er Ke Za Zhi. 2017. PMID: 28881514 Chinese.

9

[DARS mutations responsible for hypomyelination with brain stem and spinal cord involvement and leg spasticity: report of two cases and review of literature].

Zhang J, Liu M, Zhou L, Zhang ZB, Wang JM, Jiang YW, Wu Y. Zhang J, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2018 Mar 2;56(3):211-215. doi: 10.3760/cma.j.issn.0578-1310.2018.03.011. Zhonghua Er Ke Za Zhi. 2018. PMID: 29518832 Review. Chinese.

10

[Phenotype study of SCN2A gene related epilepsy].

Zeng Q, Zhang YH, Yang XL, Zhang J, Liu AJ, Liu XY, Jiang YW, Wu XR. Zeng Q, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2018 Jul 2;56(7):518-523. doi: 10.3760/cma.j.issn.0578-1310.2018.07.009. Zhonghua Er Ke Za Zhi. 2018. PMID: 29996185 Chinese.

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