Shang HF - Search Results

1

Association analysis of single-nucleotide polymorphisms of USP24 and USP40 with Parkinson's disease in the Han Chinese population.

Zhao B, Song W, Chen YP, Huang R, Chen K, Cao B, Yang Y, Shang HF. Zhao B, et al. Among authors: shang hf. Eur Neurol. 2012;68(3):181-4. doi: 10.1159/000339641. Epub 2012 Aug 24. Eur Neurol. 2012. PMID: 22923019

2

Clinical and molecular genetic evaluation of patients with primary dystonia.

Shang H, Clerc N, Lang D, Kaelin-Lang A, Burgunder JM. Shang H, et al. Eur J Neurol. 2005 Feb;12(2):131-8. doi: 10.1111/j.1468-1331.2004.00974.x. Eur J Neurol. 2005. PMID: 15679701

3

Screening of GABA(A)-receptor gene mutations in primary dystonia.

Shang H, Lang D, Burgunder JM, Kaelin-Lang A. Shang H, et al. Eur J Neurol. 2007 Oct;14(10):1179-81. doi: 10.1111/j.1468-1331.2007.01910.x. Eur J Neurol. 2007. PMID: 17880575

4

A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.

Chen XP, Zhang YW, Zhang SS, Chen Q, Burgunder JM, Wu SH, Yang Y, Luo ZM, Shang HF. Chen XP, et al. Among authors: shang hf. Mov Disord. 2008 Jul 30;23(10):1472-5. doi: 10.1002/mds.22008. Mov Disord. 2008. PMID: 18581468

5

Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west China.

Fang DF, Zhang SS, Guo XY, Zeng Y, Yang Y, Zhou D, Shang HF. Fang DF, et al. Among authors: shang hf. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):350-4. doi: 10.3109/17482960802668646. Amyotroph Lateral Scler. 2009. PMID: 19922123

6

[Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].

Chen P, Ma M, Shang H, Su D, Zhang S, Yang Y. Chen P, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Dec;26(6):626-33. doi: 10.3760/cma.j.issn.1003-9406.2009.06.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19953483 Chinese.

7

GCH1 mutation and clinical study of Chinese patients with dopa-responsive dystonia.

Liu X, Zhang SS, Fang DF, Ma MY, Guo XY, Yang Y, Shang HF. Liu X, et al. Among authors: shang hf. Mov Disord. 2010 Mar 15;25(4):447-51. doi: 10.1002/mds.22976. Mov Disord. 2010. PMID: 20108370 Clinical Trial.

8

H63D polymorphism in the hemochromatosis gene is associated with sporadic amyotrophic lateral sclerosis in China.

He X, Lu X, Hu J, Xi J, Zhou D, Shang H, Liu L, Zhou H, Yan B, Yu L, Hu F, Liu Z, He L, Yao X, Xu Y. He X, et al. Eur J Neurol. 2011 Feb;18(2):359-361. doi: 10.1111/j.1468-1331.2010.03158.x. Eur J Neurol. 2011. PMID: 20642794

9

TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis.

Huang R, Fang DF, Ma MY, Guo XY, Zhao B, Zeng Y, Zhou D, Yang Y, Shang HF. Huang R, et al. Among authors: shang hf. Neurobiol Aging. 2012 May;33(5):1015.e1-6. doi: 10.1016/j.neurobiolaging.2010.07.007. Epub 2010 Aug 13. Neurobiol Aging. 2012. PMID: 20708823

10

Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.

Ma M, Yang Y, Shang H, Su D, Zhang H, Ma Y, Liu Y, Tao D, Zhang S. Ma M, et al. J Neurol Sci. 2010 Nov 15;298(1-2):57-60. doi: 10.1016/j.jns.2010.08.024. J Neurol Sci. 2010. PMID: 20864123

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