Pan H - Search Results

1

[Screening for carrier and prenatal diagnosis of X-linked adrenoleukodystrophy].

Wang AH, Bao XH, Xiong H, Pan H, Wu Y, Zhang YH, Shi CY, Qin J, Wu XR. Wang AH, et al. Among authors: pan h. Zhonghua Er Ke Za Zhi. 2005 May;43(5):345-9. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924749 Chinese.

2

[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. Among authors: pan h. 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.

3

MECP2 gene mutation analysis in Chinese patients with Rett syndrome.

Pan H, Wang YP, Bao XH, Meng HD, Zhang Y, Wu XR, Shen Y. Pan H, et al. Eur J Hum Genet. 2002 Aug;10(8):484-6. doi: 10.1038/sj.ejhg.5200827. Eur J Hum Genet. 2002. PMID: 12111643

4

[Mutational analysis of MECP2 gene in Rett syndrome].

Pan H, Wang Y, Meng H, Bao X, Zhang Y, Shen Y, Wu X. Pan H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Aug;19(4):276-80. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12170461 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. Among authors: pan h. 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. Among authors: pan h. 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. Among authors: pan h. 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. Among authors: pan h. 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. Among authors: pan h. 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: pan h. 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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