Jiang 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: jiang 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

[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. Among authors: jiang h. 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.

3

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H. Tang B, et al. Among authors: jiang h. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

4

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. 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

5

[Mutation analysis of small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease].

Liu XM, Tang BS, Zhao GH, Xia K, Zhang FF, Pan Q, Cai F, Hu ZM, Zhang C, Chen B, Shen L, Zhang RX, Jiang H. Liu XM, et al. Among authors: jiang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):510-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215937 Chinese.

6

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia.

Jiang H, Tang B, Xia K, Hu Z, Shen L, Tang J, Zhao G, Zhang Y, Cai F, Pan Q, Long Z, Wang G, Dai H. Jiang H, et al. J Neurol Sci. 2006 Feb 15;241(1-2):1-6. doi: 10.1016/j.jns.2005.09.001. Epub 2005 Dec 27. J Neurol Sci. 2006. PMID: 16380133

7

[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. Among authors: jiang h. 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.

8

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: jiang h. 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

9

Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.

Liao SS, Shen L, Du J, Zhao GH, Wang XY, Yang Y, Xiao ZQ, Yuan Y, Jiang H, Li N, Sun HD, Wang JL, Wang CY, Zhou YF, Mo XY, Xia K, Tang BS. Liao SS, et al. Among authors: jiang h. J Neurol Sci. 2008 Dec 15;275(1-2):92-9. doi: 10.1016/j.jns.2008.07.038. Epub 2008 Oct 2. J Neurol Sci. 2008. PMID: 18835492

10

Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.

Wang YG, Du J, Wang JL, Chen J, Chen C, Luo YY, Xiao ZQ, Jiang H, Yan XX, Xia K, Pan Q, Tang BS, Shen L. Wang YG, et al. Among authors: jiang h. J Neurol Sci. 2009 Oct 15;285(1-2):121-4. doi: 10.1016/j.jns.2009.06.027. Epub 2009 Jul 15. J Neurol Sci. 2009. PMID: 19608203

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