Wu XR - Search Results

1

[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: wu y, wu xr. 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.

2

[Association of child absence epilepsy with T-STAR gene].

Chen YC, Zhang YH, Lü JJ, Pan H, Jiang YW, Liu XY, Bao XH, Ding KY, Wu HS, Xu Km, Shen Y, Wu XR. Chen YC, et al. Among authors: wu xr, wu hs. Zhonghua Yi Xue Za Zhi. 2003 Jul 10;83(13):1134-7. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12921630 Chinese.

3

[Preliminary analysis of mutations in X-linked adrenoleukodystrophy gene(ABCD1) in Chinese patients].

Xiong H, Pan H, Zhang YH, Wu XR. Xiong H, et al. Among authors: wu xr. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Oct;20(5):400-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14556192 Chinese.

4

[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: wu y, wu xr. 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.

5

[Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis].

Bao XH, Pan H, Song FY, Wu XR. Bao XH, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2004 Apr;42(4):252-5. Zhonghua Er Ke Za Zhi. 2004. PMID: 15157382 Chinese.

6

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: wu y, wu xr. Pediatr Neurol. 2005 Aug;33(2):114-20. doi: 10.1016/j.pediatrneurol.2005.03.006. Pediatr Neurol. 2005. PMID: 16087056

7

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: wu y, wu xr. 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.

8

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.

Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR. Yang YL, et al. Among authors: wu xr. Chin Med J (Engl). 2006 Mar 5;119(5):373-7. Chin Med J (Engl). 2006. PMID: 16542579

9

[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome].

Li MR, Pan H, Bao XH, Zhang YZ, Jiang SL, Wu XR. Li MR, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2006 Apr;44(4):285-8. Zhonghua Er Ke Za Zhi. 2006. PMID: 16780651 Chinese.

10

[The effect of CACNA1H gene G773D mutation on calcium channel function].

Wang JL, Han CY, Jing YH, Chen YC, Feng N, Lu JJ, Zhang YH, Pan H, Wu HS, Xu KM, Jiang YW, Liang JM, Wang L, Wang XL, Shen Y, Wu XR. Wang JL, et al. Among authors: wu xr, wu hs. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Aug;23(4):369-73. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16883519 Chinese.

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