Li H - Search Results

1

A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family.

Tang B, Li H, Xia K, Jiang H, Pan Q, Shen L, Long Z, Zhao G, Cai F. Tang B, et al. Among authors: li h. J Neurol Sci. 2004 Jun 15;221(1-2):31-4. doi: 10.1016/j.jns.2004.03.001. J Neurol Sci. 2004. PMID: 15178210

2

Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.

Jiang H, Tang B, Xia K, Zhou Y, Xu B, Zhao G, Li H, Shen L, Pan Q, Cai F. Jiang H, et al. Among authors: li h. J Neurol Sci. 2005 Sep 15;236(1-2):25-9. doi: 10.1016/j.jns.2005.04.009. J Neurol Sci. 2005. PMID: 15979648

3

A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.

Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B. Li H, et al. Among authors: li n. Epilepsy Res. 2008 Mar;79(1):1-5. doi: 10.1016/j.eplepsyres.2007.12.005. Epub 2008 Feb 4. Epilepsy Res. 2008. PMID: 18249525

4

Mutation detection in candidate genes for benign familial infantile seizures on a novel locus.

Li N, Li H, Jiang H, Shen L, Yan X, Guo J, Song Y, Yang Q, Wang Y, Li X, Xiang R, Zi X, Long X, Hu Z, Pan Q, Xia K, Tang B. Li N, et al. Among authors: li h, li x. Int J Neurosci. 2010 Mar;120(3):217-21. doi: 10.3109/00207450903477779. Int J Neurosci. 2010. PMID: 20374090

5

[Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].

Li HY, Tang BS, Yan XX, Guo JF, Shen L, Song YM, Jiang H, Xia K, Xie ZG, Yang QA. Li HY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Aug;23(4):374-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16883520 Chinese.

6

[A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions].

Li HY, Tang BS, Zhang AM, Cao QH, Meng GL, Jiang H, Shen L. Li HY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Dec;20(6):482-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14669214 Chinese.

7

[A novel mutation of SCN4A gene causes hypokalemic periodic paralysis in a Chinese family].

Li HY, Zhou XL, Guo JF, Tang BS, Fu YJ, Sun JY. Li HY, et al. Zhonghua Yi Xue Za Zhi. 2020 Dec 8;100(45):3622-3625. doi: 10.3760/cma.j.cn112137-20200421-01265. Zhonghua Yi Xue Za Zhi. 2020. PMID: 33333687 Chinese.

8

[TH gene mutation in Chinese patients with autosomal recessive dopa-responsive dystonia].

Liu W, Tang BS, Cao GF, Chen T, Li HY. Liu W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Oct;21(5):452-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15476168 Chinese.

9

A novel genetic locus for benign familial infantile seizures maps to chromosome 1p36.12-p35.1.

Li HY, Li N, Jiang H, Shen L, Guo JF, Zhang RX, Xia K, Pan Q, Zi XH, Tang BS. Li HY, et al. Among authors: li n. Clin Genet. 2008 Nov;74(5):490-2. doi: 10.1111/j.1399-0004.2008.01092.x. Epub 2008 Sep 20. Clin Genet. 2008. PMID: 18811698 No abstract available.

10

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study.

Tian WT, Zhan FX, Liu ZH, Liu Z, Liu Q, Guo XN, Zhou ZW, Wang SG, Liu XR, Jiang H, Li XH, Zhao GH, Li HY, Tang JG, Bi GH, Zhong P, Yin XM, Liu TT, Ni RL, Zheng HR, Liu XL, Qian XH, Wu JY, Cao YW, Zhang C, Liu SH, Wu YY, Wang QF, Xu T, Hou WZ, Li ZY, Ke HY, Zhu ZY, Zheng L, Wang T, Rong TY, Wu L, Zhang Y, Fang K, Wang ZH, Zhang YK, Zhang M, Zhao YW, Tang BS, Luan XH, Huang XJ, Cao L. Tian WT, et al. Among authors: li zy, li xh, li hy. Mov Disord. 2022 Mar;37(3):545-552. doi: 10.1002/mds.28865. Epub 2021 Nov 24. Mov Disord. 2022. PMID: 34820915

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