Jiang Y - Search Results

1

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.

Yang Y, Zeng Q, Cheng M, Niu X, Xiangwei W, Gong P, Li W, Ma J, Zhang X, Yang X, Yang Z, Sun D, Zhou S, Liao J, Jiang Y, Zhang Y. Yang Y, et al. Among authors: jiang y. J Neurol. 2022 May;269(5):2649-2665. doi: 10.1007/s00415-021-10834-w. Epub 2021 Oct 26. J Neurol. 2022. PMID: 34698933

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: jiang y. 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

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: jiang y. Neurosci Lett. 2002 Oct 31;332(2):75-8. doi: 10.1016/s0304-3940(02)00805-4. Neurosci Lett. 2002. PMID: 12384214 Clinical Trial.

4

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: jiang y. Neurosci Lett. 2003 Jun 12;343(3):151-4. doi: 10.1016/s0304-3940(03)00316-1. Neurosci Lett. 2003. PMID: 12770685

5

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: jiang y. Ann Neurol. 2003 Aug;54(2):239-43. doi: 10.1002/ana.10607. Ann Neurol. 2003. PMID: 12891677

6

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

7

[Clinical characteristics of alternating hemiplegia of childhood in 13 patients].

Zhang YH, Sun WX, Qin J, Jiang YW, Wu XR. Zhang YH, et al. Zhonghua Er Ke Za Zhi. 2003 Sep;41(9):680-3. Zhonghua Er Ke Za Zhi. 2003. PMID: 14733811 Chinese.

8

[Clinical observation and long-term follow-up of benign infantile epilepsy].

Liu XY, Jiang YW, Wu J, Feng BR, Zhang YP, Lin Q. Liu XY, et al. Zhonghua Er Ke Za Zhi. 2003 Jan;41(1):14-6. Zhonghua Er Ke Za Zhi. 2003. PMID: 14761317 Chinese.

9

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: jiang yw. Chin Med J (Engl). 2004 Oct;117(10):1497-501. Chin Med J (Engl). 2004. PMID: 15498372

10

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

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