Hu F - Search Results

1

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. Among authors: hu f. 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

2

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. Among authors: hu f. 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

3

Pilot association study of oxcarbazepine-induced mild cutaneous adverse reactions with HLA-B*1502 allele in Chinese Han population.

Hu FY, Wu XT, An DM, Yan B, Stefan H, Zhou D. Hu FY, et al. Seizure. 2011 Mar;20(2):160-2. doi: 10.1016/j.seizure.2010.11.014. Epub 2010 Dec 18. Seizure. 2011. PMID: 21169036 Free article.

4

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.

5

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. Among authors: hu f. 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.

6

Predictive markers for carbamazepine and lamotrigine-induced maculopapular exanthema in Han Chinese.

Li LJ, Hu FY, Wu XT, An DM, Yan B, Zhou D. Li LJ, et al. Epilepsy Res. 2013 Sep;106(1-2):296-300. doi: 10.1016/j.eplepsyres.2013.05.004. Epub 2013 Jul 5. Epilepsy Res. 2013. PMID: 23830818

7

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. Int J Stroke. 2013 Aug;8(6):E35. doi: 10.1111/ijs.12076. Int J Stroke. 2013. PMID: 23879759 No abstract available.

8

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. Int J Stroke. 2013 Oct;8(7):E43. doi: 10.1111/ijs.12074. Int J Stroke. 2013. PMID: 24024919 No abstract available.

9

Prevalence of restless legs syndrome in Parkinson's disease: a systematic review and meta-analysis of observational studies.

Yang X, Liu B, Shen H, Li S, Zhao Q, An R, Hu F, Ren H, Xu Y, Xu Z. Yang X, et al. Among authors: hu f. Sleep Med. 2018 Mar;43:40-46. doi: 10.1016/j.sleep.2017.11.1146. Epub 2018 Jan 31. Sleep Med. 2018. PMID: 29482811

10

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. Among authors: hu f. 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.

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