Jiang H - Search Results

1

Increase of the plasma α-synuclein levels in patients with multiple system atrophy.

Sun ZF, Xiang XS, Chen Z, Zhang L, Tang BS, Xia K, Jiang H. Sun ZF, et al. Among authors: jiang h. Mov Disord. 2014 Mar;29(3):375-9. doi: 10.1002/mds.25688. Epub 2013 Sep 30. Mov Disord. 2014. PMID: 24115000

2

SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population.

Sun Z, Xiang X, Tang B, Chen Z, Peng H, Xia K, Jiang H. Sun Z, et al. Among authors: jiang h. Int J Neurosci. 2015;125(8):612-5. doi: 10.3109/00207454.2014.990013. Epub 2015 Jan 5. Int J Neurosci. 2015. PMID: 25427997

3

Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.

Jiang H, Tang BS, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K. Jiang H, et al. Chin Med J (Engl). 2005 May 20;118(10):837-43. Chin Med J (Engl). 2005. PMID: 15989765

4

[The advances in research on phosphorylation of polyglutamine disease].

Zhou YF, Jiang H, Tang JG, Tang BS. Zhou YF, et al. Among authors: jiang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):414-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18683139 Review. Chinese.

5

Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.

Guo JF, Xiao B, Liao B, Zhang XW, Nie LL, Zhang YH, Shen L, Jiang H, Xia K, Pan Q, Yan XX, Tang BS. Guo JF, et al. Among authors: jiang h. Mov Disord. 2008 Oct 30;23(14):2074-9. doi: 10.1002/mds.22156. Mov Disord. 2008. PMID: 18785233

6

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.

Wang JL, Xiao B, Cui XX, Guo JF, Lei LF, Song XW, Shen L, Jiang H, Yan XX, Pan Q, Long ZG, Xia K, Tang BS. Wang JL, et al. Among authors: jiang h. Mov Disord. 2009 Oct 15;24(13):2007-11. doi: 10.1002/mds.22727. Mov Disord. 2009. PMID: 19672991

7

Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindreds.

Jia D, Tang B, Chen Z, Shi Y, Sun Z, Zhang L, Wang J, Xia K, Jiang H. Jia D, et al. Among authors: jiang h. Int J Neurosci. 2012 Oct;122(10):560-2. doi: 10.3109/00207454.2012.690796. Epub 2012 Jun 22. Int J Neurosci. 2012. PMID: 22563911

8

Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population.

Chen Z, Li X, Tang B, Wang J, Shi Y, Sun Z, Zhang L, Pan Q, Xia K, Jiang H. Chen Z, et al. Among authors: jiang h. Neurosci Lett. 2012 Jun 27;520(1):16-9. doi: 10.1016/j.neulet.2012.05.008. Epub 2012 May 11. Neurosci Lett. 2012. PMID: 22579694

9

[Spinal muscular atrophy mimicking myotonic dystrophy: a case report and clinical, pathological and genetic analysis].

Luo LX, Pan Q, Xia K, Tang BS, Jiang H. Luo LX, et al. Among authors: jiang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):455-8. doi: 10.3760/cma.j.issn.1003-9406.2012.04.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875506 Chinese.

10

Spinocerebellar ataxia type 13 is an uncommon SCA subtype in the Chinese Han population.

Peng L, Wang C, Chen Z, Wang JL, Tang BS, Jiang H. Peng L, et al. Among authors: jiang h. Int J Neurosci. 2013 Jul;123(7):450-3. doi: 10.3109/00207454.2013.763254. Epub 2013 Feb 11. Int J Neurosci. 2013. PMID: 23293936

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