Xu KM - Search Results

1

Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.

Lü JJ, Zhang YH, Pan H, Chen YC, Liu XY, Jiang YW, Bao XH, Shen Y, Wu HS, Xu KM, Wu XR. Lü JJ, et al. Among authors: xu km. Chin Med J (Engl). 2004 Oct;117(10):1497-501. Chin Med J (Engl). 2004. PMID: 15498372

2

[T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy].

Lü JJ, Zhang YH, Chen YC, Pan H, Wang JL, Zhang L, Wu HS, Xu KM, Liu XY, Tao LD, Shen Y, Wu XR. Lü JJ, et al. Among authors: xu km. Zhonghua Er Ke Za Zhi. 2005 Feb;43(2):133-6. Zhonghua Er Ke Za Zhi. 2005. PMID: 15833171 Chinese.

3

[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: xu km. 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.

4

[Case-control study and transmission/disequilibrium test of childhood absence epilepsy].

Lu J, Chen Y, Zhang Y, Pan H, Liu X, Jiang Y, Du W, Shen Y, Xu K, Wu H, Wu X. Lu J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Jun;19(3):183-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12048673 Chinese.

5

[Association analysis of childhood absence epilepsy by microsatellite DNA].

Lu J, Chen Y, Pan H, Zhang Y, Jiang Y, Di W, Shen Y, Xu K, Wu H, Wu X. Lu J, et al. Zhonghua Yi Xue Za Zhi. 2002 Aug 10;82(15):1029-32. Zhonghua Yi Xue Za Zhi. 2002. PMID: 12194792 Chinese.

6

Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy.

Lu J, Chen Y, Zhang Y, Pan H, Wu H, Xu K, Liu X, Jiang Y, Bao X, Ding K, Shen Y, Wu X. Lu J, et al. Neurosci Lett. 2002 Oct 31;332(2):75-8. doi: 10.1016/s0304-3940(02)00805-4. Neurosci Lett. 2002. PMID: 12384214 Clinical Trial.

7

T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population.

Chen Y, Lu J, Zhang Y, Pan H, Wu H, Xu K, Liu X, Jiang Y, Bao X, Zhou J, Liu W, Shi G, Shen Y, Wu X. Chen Y, et al. Neurosci Lett. 2003 Apr 24;341(1):29-32. doi: 10.1016/s0304-3940(03)00124-1. Neurosci Lett. 2003. PMID: 12676336

8

The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han population.

Lu J, Chen Y, Pan H, Zhang Y, Wu H, Xu K, Liu X, Jiang Y, Bao X, Shen Y, Wu X. Lu J, et al. Neurosci Lett. 2003 Jun 12;343(3):151-4. doi: 10.1016/s0304-3940(03)00316-1. Neurosci Lett. 2003. PMID: 12770685

9

Association between genetic variation of CACNA1H and childhood absence epilepsy.

Chen Y, Lu J, Pan H, Zhang Y, Wu H, Xu K, Liu X, Jiang Y, Bao X, Yao Z, Ding K, Lo WH, Qiang B, Chan P, Shen Y, Wu X. Chen Y, et al. Ann Neurol. 2003 Aug;54(2):239-43. doi: 10.1002/ana.10607. Ann Neurol. 2003. PMID: 12891677

10

[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: xu km. Zhonghua Yi Xue Za Zhi. 2003 Jul 10;83(13):1134-7. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12921630 Chinese.

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