Jiang H - Search Results

1

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.

Wang JL, Yang X, Xia K, Hu ZM, Weng L, Jin X, Jiang H, Zhang P, Shen L, Guo JF, Li N, Li YR, Lei LF, Zhou J, Du J, Zhou YF, Pan Q, Wang J, Wang J, Li RQ, Tang BS. Wang JL, et al. Among authors: jiang h. Brain. 2010 Dec;133(Pt 12):3510-8. doi: 10.1093/brain/awq323. Epub 2010 Nov 23. Brain. 2010. PMID: 21106500

2

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

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: 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

4

Spinocerebellar ataxia type 11 in the Chinese Han population.

Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, Jiang H, Xia K, Pan Q, Tang B. Xu Q, et al. Among authors: jiang h. Neurol Sci. 2010 Feb;31(1):107-9. doi: 10.1007/s10072-009-0129-4. Epub 2009 Sep 19. Neurol Sci. 2010. PMID: 19768375

5

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.

Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L. Du J, et al. Among authors: jiang h. Clin Neurol Neurosurg. 2011 Jul;113(6):480-2. doi: 10.1016/j.clineuro.2011.02.011. Epub 2011 Mar 17. Clin Neurol Neurosurg. 2011. PMID: 21419568

6

Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.

Wang J, Shen L, Lei L, Xu Q, Zhou J, Liu Y, Guan W, Pan Q, Xia K, Tang B, Jiang H. Wang J, et al. Among authors: jiang h. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Jun;36(6):482-9. doi: 10.3969/j.issn.1672-7347.2011.06.003. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 21743138

7

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.

Wang JL, Cao L, Li XH, Hu ZM, Li JD, Zhang JG, Liang Y, San-A, Li N, Chen SQ, Guo JF, Jiang H, Shen L, Zheng L, Mao X, Yan WQ, Zhou Y, Shi YT, Ai SX, Dai MZ, Zhang P, Xia K, Chen SD, Tang BS. Wang JL, et al. Among authors: jiang h. Brain. 2011 Dec;134(Pt 12):3493-3501. doi: 10.1093/brain/awr289. Epub 2011 Nov 26. Brain. 2011. PMID: 22120146 Free PMC article.

8

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

9

[Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].

Jiang H, Tang B, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K. Jiang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):1-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696468 Chinese.

10

[ATM gene mutations in Chinese patients with ataxia telangiectasia].

Jiang H, Tang B, Hu Z, Xia K, Xu B, Tang J, Shen L. Jiang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):121-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793768 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

28,917 results

Search Page

Filters