Jiang Y - Search Results

1

Congenital muscular dystrophies in China.

Ge L, Zhang C, Wang Z, Chan SHS, Zhu W, Han C, Zhang X, Zheng H, Wu L, Jin B, Shan J, Mao B, Zhong J, Peng X, Cheng Y, Hu J, Sun Y, Lu J, Hua Y, Zhu S, Wei C, Wang S, Jiao H, Yang H, Fu X, Fan Y, Chang X, Wang S, Bao X, Zhang Y, Wang J, Wu Y, Jiang Y, Yuan Y, Rutkowski A, Bönnemann CG, Wei W, Wu X, Xiong H. Ge L, et al. Among authors: jiang y. Clin Genet. 2019 Sep;96(3):207-215. doi: 10.1111/cge.13560. Epub 2019 Jun 6. Clin Genet. 2019. PMID: 31066047

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

Neuropathologic and clinical features in eight Chinese patients with Leigh disease.

Jiang YW, Qin J, Yuan Y, Qi Y, Wu XR. Jiang YW, et al. J Child Neurol. 2002 Jun;17(6):450-2. doi: 10.1177/088307380201700611. J Child Neurol. 2002. PMID: 12174968

4

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.

5

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: jiang y. Neurosci Lett. 2003 Apr 24;341(1):29-32. doi: 10.1016/s0304-3940(03)00124-1. Neurosci Lett. 2003. PMID: 12676336

6

Joint meeting of 9th International Child Neurology Congress (ICNC) and the 7th Asian and Oceanian Congress of Child Neurology (AOCCN), Beijing, September 20-25, 2002.

Wu XR, Jiang YW, Bao XH. Wu XR, et al. J Child Neurol. 2003 Feb;18(2):131-2. doi: 10.1177/08830738030180021601. J Child Neurol. 2003. PMID: 12693781 No abstract available.

7

Effect of recurrent epileptiform discharges induced by magnesium-free treatment on developing cortical neurons in vitro.

Cao HY, Jiang YW, Liu ZW, Wu XR. Cao HY, et al. Brain Res Dev Brain Res. 2003 Apr 14;142(1):1-6. doi: 10.1016/s0165-3806(03)00005-1. Brain Res Dev Brain Res. 2003. PMID: 12694939

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

10

[Long-term effects of recurrent seizures in neonatal rats on NMDA receptor expression in the brain].

Bo T, Jiang Y, Cao H, Wang J, Wu X. Bo T, et al. Among authors: jiang y. Beijing Da Xue Xue Bao Yi Xue Ban. 2003 Jun 18;35(3):292-5. Beijing Da Xue Xue Bao Yi Xue Ban. 2003. PMID: 12914249 Free article. Chinese.

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