Shang HF - Search Results

1

The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.

Chen YP, Yu SH, Zhang GH, Hou YB, Gu XJ, Ou RW, Shen Y, Song W, Chen XP, Zhao B, Cao B, Zhang LY, Sun MM, Liu FF, Wei QQ, Liu KC, Lin JY, Yang TM, Yang J, Wu Y, Jiang Z, Liu J, Cheng YF, Xiao Y, Su WM, Feng F, Cai YY, Li SR, Hu T, Yuan XQ, Zhou QQ, Shao N, Ma S, Shang HF. Chen YP, et al. Among authors: shang hf. Eur J Neurol. 2022 Nov;29(11):3218-3228. doi: 10.1111/ene.15509. Epub 2022 Aug 4. Eur J Neurol. 2022. PMID: 35861376

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

RNA interference-mediated inhibition of wild-type Torsin A expression increases apoptosis caused by oxidative stress in cultured cells.

Chen XP, Hu XH, Wu SH, Zhang YW, Xiao B, Shang HF. Chen XP, et al. Among authors: shang hf. Neurochem Res. 2010 Aug;35(8):1214-23. doi: 10.1007/s11064-010-0177-4. Epub 2010 May 9. Neurochem Res. 2010. PMID: 20455020

7

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

8

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

9

Causes and places of death of patients with amyotrophic lateral sclerosis in south-west China.

Yang R, Huang R, Chen D, Song W, Zeng Y, Zhao B, Zhou D, Shang HF. Yang R, et al. Among authors: shang hf. Amyotroph Lateral Scler. 2011 May;12(3):206-9. doi: 10.3109/17482968.2011.572979. Epub 2011 Apr 21. Amyotroph Lateral Scler. 2011. PMID: 21506897

10

A meta-analysis of diffusion tensor imaging studies in amyotrophic lateral sclerosis.

Li J, Pan P, Song W, Huang R, Chen K, Shang H. Li J, et al. Neurobiol Aging. 2012 Aug;33(8):1833-8. doi: 10.1016/j.neurobiolaging.2011.04.007. Epub 2011 May 28. Neurobiol Aging. 2012. PMID: 21621298 Review.

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