Jiang H - Search Results

1

Spinocerebellar ataxia type 21 exists in the Chinese Han population.

Zeng S, Zeng J, He M, Zeng X, Zhou Y, Liu Z, Xia K, Pan Q, Jiang H, Shen L, Yan X, Tang B, Wang J. Zeng S, et al. Among authors: jiang h. Sci Rep. 2016 Jan 27;6:19897. doi: 10.1038/srep19897. Sci Rep. 2016. PMID: 26813285 Free PMC article.

2

Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population.

Zeng J, Wang J, Zeng S, He M, Zeng X, Zhou Y, Liu Z, Jiang H, Tang B. Zeng J, et al. Among authors: jiang h. J Neurol Sci. 2015 Apr 15;351(1-2):124-126. doi: 10.1016/j.jns.2015.03.002. Epub 2015 Mar 6. J Neurol Sci. 2015. PMID: 25765228

3

SCA38 is rare in Mainland China.

Liu Z, Zeng S, Zeng J, Zhou Y, Zeng X, Jiang H, Shen L, Tang B, Wang J. Liu Z, et al. Among authors: jiang h. J Neurol Sci. 2015 Nov 15;358(1-2):333-4. doi: 10.1016/j.jns.2015.09.350. Epub 2015 Sep 15. J Neurol Sci. 2015. PMID: 26433464

4

C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland China.

He M, Yan WQ, Zeng S, Liu Z, Zhou Y, Zeng XF, Zeng JS, Jiang H, Shen L, Tang BS, Wang JL. He M, et al. Among authors: jiang h. J Neurol Sci. 2016 Feb 15;361:181-3. doi: 10.1016/j.jns.2015.12.034. Epub 2015 Dec 22. J Neurol Sci. 2016. PMID: 26810537

5

Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease.

Sun Z, Jia D, Shi Y, Hou X, Yang X, Guo J, Li N, Wang J, Sun Q, Zhang H, Lei L, Shen L, Yan X, Xia K, Jiang H, Tang B. Sun Z, et al. Among authors: jiang h. Sci Rep. 2016 Feb 12;6:21649. doi: 10.1038/srep21649. Sci Rep. 2016. PMID: 26867507 Free PMC article.

6

Polygenic determinants of Parkinson's disease in a Chinese population.

Guo JF, Li K, Yu RL, Sun QY, Wang L, Yao LY, Hu YC, Lv ZY, Luo LZ, Shen L, Jiang H, Yan XX, Pan Q, Xia K, Tang BS. Guo JF, et al. Among authors: jiang h. Neurobiol Aging. 2015 Apr;36(4):1765.e1-1765.e6. doi: 10.1016/j.neurobiolaging.2014.12.030. Epub 2015 Jan 6. Neurobiol Aging. 2015. PMID: 25623333

7

Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.

Long Z, Chen Z, Wang C, Huang F, Peng H, Hou X, Ding D, Ye W, Wang J, Pan Q, Li J, Xia K, Tang B, Ashizawa T, Jiang H. Long Z, et al. Among authors: jiang h. PLoS One. 2015 Feb 17;10(2):e0117488. doi: 10.1371/journal.pone.0117488. eCollection 2015. PLoS One. 2015. PMID: 25689313 Free PMC article.

8

C9orf72 hexanucleotide expansion analysis in Chinese patients with multiple system atrophy.

Sun Z, Jiang H, Jiao B, Hou X, Shen L, Xia K, Tang B. Sun Z, et al. Among authors: jiang h. Parkinsonism Relat Disord. 2015 Jul;21(7):811-2. doi: 10.1016/j.parkreldis.2015.04.008. Epub 2015 Apr 18. Parkinsonism Relat Disord. 2015. PMID: 25934183 No abstract available.

9

Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from China.

Wang C, Chen Z, Yang F, Jiao B, Peng H, Shi Y, Wang Y, Huang F, Wang J, Shen L, Xia K, Tang B, Ashizawa T, Jiang H. Wang C, et al. Among authors: jiang h. PLoS One. 2015 Jun 17;10(6):e0130336. doi: 10.1371/journal.pone.0130336. eCollection 2015. PLoS One. 2015. PMID: 26083476 Free PMC article.

10

Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective.

Chen Z, Ye W, Long Z, Ding D, Peng H, Hou X, Qiu R, Xia K, Tang B, Jiang H. Chen Z, et al. Among authors: jiang h. PLoS One. 2015 Oct 6;10(10):e0139738. doi: 10.1371/journal.pone.0139738. eCollection 2015. PLoS One. 2015. PMID: 26439923 Free PMC article.

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

29,466 results

Search Page

Filters