Jiang YW - Search Results

1

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.

Zhang ZB, Tian MQ, Gao K, Jiang YW, Wu Y. Zhang ZB, et al. Among authors: jiang yw. Mov Disord. 2015 Aug;30(9):1290-2. doi: 10.1002/mds.26216. Epub 2015 Jul 21. Mov Disord. 2015. PMID: 26195193 No abstract available.

2

[X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China].

Pan H, Xiong H, Zhang YH, Wu Y, Bao XH, Jiang YW, Wu XR. Pan H, et al. Among authors: jiang yw. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):1-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767898 Chinese.

3

ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophy.

Pan H, Xiong H, Wu Y, Zhang YH, Bao XH, Jiang YW, Wu XR. Pan H, et al. Among authors: jiang yw. Pediatr Neurol. 2005 Aug;33(2):114-20. doi: 10.1016/j.pediatrneurol.2005.03.006. Pediatr Neurol. 2005. PMID: 16087056

4

The genotype and phenotype studies of 40 Chinese patients with X-linked adrenoleukodystrophy (X-ALD).

Ping LL, Bao XH, Wang AH, Pan H, Wu Y, Xiong H, Zhang YH, Jiang YW, Qin J, Wu XR. Ping LL, et al. Among authors: jiang yw. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):66-70. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415970 Free article.

5

[Clinical characteristics and long-term prognosis of Landau-Kleffner syndrome].

Wang S, Zhang YH, Bao XH, Wu Y, Jiang YW, Liu XY, Qin J. Wang S, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2006 Feb;44(2):105-9. Zhonghua Er Ke Za Zhi. 2006. PMID: 16624025 Chinese.

6

[Analysis of ARSA mutations in a Chinese family with metachromatic leukodystrophy].

Wang JM, Jiang YW, Shi HP, Zhang WM, Pan H, Bao XH, Wu Y, Qin J, Wu XR. Wang JM, et al. Among authors: jiang yw. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Aug;23(4):378-82. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16883521 Chinese.

7

[Diagnostic value of muscle, sural nerve and skin biopsies in childhood neuromuscular disorders].

Chang XZ, Zhou JY, Yuan Y, Wu Y, Li YX, Zhang W, Jiang YW, Bao XH, Zhang YH, Wang S, Xiong H, Yang YL, Qin J. Chang XZ, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2006 Dec;44(12):909-12. Zhonghua Er Ke Za Zhi. 2006. PMID: 17254458 Chinese.

8

[Clinical characteristics of cases with leukoencephalopathy with vanishing white matter].

Wu Y, Jiang YW, Qin J, Xiao JX, Wang JM, Yang YL, Zhang YH, Chang XZ, Lin Q, Wu XR. Wu Y, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2007 Feb;45(2):115-20. Zhonghua Er Ke Za Zhi. 2007. PMID: 17456339 Chinese.

9

[Clinical features and genotype-phenotype studies of 89 Chinese patients with X-linked adrenoleukodystrophy].

Ping LL, Bao XH, Wang AH, Pan H, Wu Y, Xiong H, Jiang YW, Qin J, Wu XR. Ping LL, et al. Among authors: jiang yw. Zhonghua Er Ke Za Zhi. 2007 Mar;45(3):203-7. Zhonghua Er Ke Za Zhi. 2007. PMID: 17504626 Chinese.

10

ARSA gene mutations in five Chinese metachromatic leukodystrophy patients.

Wang J, Zhang W, Pan H, Bao X, Wu Y, Wu X, Jiang Y. Wang J, et al. Pediatr Neurol. 2007 Jun;36(6):397-401. doi: 10.1016/j.pediatrneurol.2007.02.011. Pediatr Neurol. 2007. PMID: 17560502

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