Xu YM - Search Results

1

ACTA2 is not a major responsible gene for spontaneous cerebral artery dissection.

Hu FY, Zheng HB, Xu YM, Jiang Y, Guo HZ, Zhou D. Hu FY, et al. Among authors: xu ym. Int J Stroke. 2013 Aug;8(6):E35. doi: 10.1111/ijs.12076. Int J Stroke. 2013. PMID: 23879759 No abstract available.

2

ACTA2 is not a major genetic risk gene for Chinese patients with moyamoya disease.

Hu FY, Zheng HB, Xu YM, Jiang Y, Zhou D. Hu FY, et al. Among authors: xu ym. Int J Stroke. 2013 Oct;8(7):E43. doi: 10.1111/ijs.12074. Int J Stroke. 2013. PMID: 24024919 No abstract available.

3

Novel human pathological mutations. Gene symbol: GCH1. Disease: dystonia, dopa-responsive.

Hu F, Xu Y, Zhou D, He X, Yu L. Hu F, et al. Hum Genet. 2010 Apr;127(4):482. Hum Genet. 2010. PMID: 21488304 No abstract available.

4

LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China.

Yu L, Hu F, Zou X, Jiang Y, Liu Y, He X, Xi J, Liu L, Liu Z, He L, Xu Y. Yu L, et al. Brain Res. 2009 Nov 3;1296:113-6. doi: 10.1016/j.brainres.2009.08.047. Epub 2009 Aug 20. Brain Res. 2009. PMID: 19699188

5

SNP rs7684318 of the alpha-synuclein gene is associated with Parkinson's disease in the Han Chinese population.

Yu L, Xu P, He X, Hu F, Lin Z, Zhu M, Liu Z, He L, Xu Y. Yu L, et al. Brain Res. 2010 Jul 30;1346:262-5. doi: 10.1016/j.brainres.2010.05.069. Epub 2010 Jun 1. Brain Res. 2010. PMID: 20513365

6

Two novel mutations of the GTP cyclohydrolase 1 gene and genotype-phenotype correlation in Chinese Dopa-responsive dystonia patients.

Yu L, Zhou H, Hu F, Xu Y. Yu L, et al. Eur J Hum Genet. 2013 Jul;21(7):731-5. doi: 10.1038/ejhg.2012.239. Epub 2012 Dec 5. Eur J Hum Genet. 2013. PMID: 23211702 Free PMC article.

7

[Clinical characteristics and spastin gene mutation analysis on an autosomal dominant kindred with hereditary spastic paraplegia].

Liu L, Liu YQ, Xu YM, Xue R, Tang YF, Zhao LL, Liu YH, Zhou D. Liu L, et al. Among authors: xu ym. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Apr;24(2):224-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17407089 Chinese.

8

Meta-analysis of the association between ZNF512B polymorphism rs2275294 and risk of amyotrophic lateral sclerosis.

Ning P, Yang X, Yang B, Zhao Q, Huang H, An R, Chen Y, Hu F, Xu Z, Xu Y. Ning P, et al. Neurol Sci. 2018 Jul;39(7):1261-1266. doi: 10.1007/s10072-018-3411-5. Epub 2018 May 1. Neurol Sci. 2018. PMID: 29713939 Review.

9

Systematic review of the prognostic role of body mass index in amyotrophic lateral sclerosis.

Ning P, Yang B, Li S, Mu X, Shen Q, Hu F, Tang Y, Yang X, Xu Y. Ning P, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Aug;20(5-6):356-367. doi: 10.1080/21678421.2019.1587631. Epub 2019 Apr 1. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30931632

10

Structural and functional changes mapped in the brains of amyotrophic lateral sclerosis patients with/without dysphagia: a pilot study.

Li S, Chen Q, Yu B, Xue K, Luo C, Xu Y, Gong Q, He C, Zhou D, He L, Yao D. Li S, et al. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):280-7. doi: 10.3109/17482960902893342. Amyotroph Lateral Scler. 2009. PMID: 19922114

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