Huang H - Search Results

1

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: huang h. 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.

2

Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.

Tian S, Yang X, Zhao Q, Zheng J, Huang H, Chen Y, An R, Xu Y. Tian S, et al. Among authors: huang h. Neurosci Lett. 2017 Mar 6;642:119-122. doi: 10.1016/j.neulet.2017.02.008. Epub 2017 Feb 6. Neurosci Lett. 2017. PMID: 28179208

3

Onset of bladder and motor symptoms in multiple system atrophy: differences according to phenotype.

Zheng J, Yang X, Chen Y, Zhao Q, Tian S, Huang H, Xu Y. Zheng J, et al. Among authors: huang h. Clin Auton Res. 2017 Apr;27(2):103-106. doi: 10.1007/s10286-017-0405-y. Epub 2017 Feb 11. Clin Auton Res. 2017. PMID: 28190176

4

Association between gene polymorphism and depression in Parkinson's disease: A case-control study.

Zheng J, Yang X, Zhao Q, Tian S, Huang H, Chen Y, Xu Y. Zheng J, et al. Among authors: huang h. J Neurol Sci. 2017 Apr 15;375:231-234. doi: 10.1016/j.jns.2017.02.001. Epub 2017 Feb 3. J Neurol Sci. 2017. PMID: 28320136

5

Sequence TMEM230 gene in patients with multiple system atrophy in a southwest Chinese population: A pilot study.

Yang X, An R, Xi J, Zhen J, Chen Y, Huang H, Tian S, Zhao Q, Ning P, Xu Y. Yang X, et al. Among authors: huang h. J Neurol Sci. 2017 Apr 15;375:264-265. doi: 10.1016/j.jns.2017.02.006. Epub 2017 Feb 3. J Neurol Sci. 2017. PMID: 28320143 No abstract available.

6

Festination Correlates with SNCA Polymorphism in Chinese Patients with Parkinson's Disease.

Zheng J, Yang X, Zhao Q, Tian S, Huang H, Chen Y, Xu Y. Zheng J, et al. Among authors: huang h. Parkinsons Dis. 2017;2017:3176805. doi: 10.1155/2017/3176805. Epub 2017 Mar 5. Parkinsons Dis. 2017. PMID: 28357149 Free PMC article.

7

Sequencing TMEM230 in Chinese patients with sporadic or familial Parkinson's disease.

Yang X, An R, Xi J, Zheng J, Chen Y, Huang H, Tian S, Zhao Q, Ning P, Xu Y. Yang X, et al. Among authors: huang h. Mov Disord. 2017 May;32(5):800-802. doi: 10.1002/mds.26996. Epub 2017 Apr 3. Mov Disord. 2017. PMID: 28370613 No abstract available.

8

Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.

Yang X, Zheng J, An R, Tian S, Zhao Q, Chen Y, Huang H, Ning PP, Song Y, Xu Y. Yang X, et al. Among authors: huang h. Neurosci Lett. 2017 May 22;650:8-11. doi: 10.1016/j.neulet.2017.04.003. Epub 2017 Apr 3. Neurosci Lett. 2017. PMID: 28380328

9

No association of PARK10 polymorphism with Parkinson's disease in Han Chinese population.

Tian S, Yang X, Zhao Q, Zheng J, Huang H, Chen Y, An R, Xu Y. Tian S, et al. Among authors: huang h. Parkinsonism Relat Disord. 2017 Sep;42:105-106. doi: 10.1016/j.parkreldis.2017.06.005. Epub 2017 Jun 12. Parkinsonism Relat Disord. 2017. PMID: 28651751 No abstract available.

10

Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population.

Xi J, Yang X, Zhao Q, Zheng J, An R, Tian S, Huang H, Hu F, Ning P, Xu Y. Xi J, et al. Among authors: huang h. Neurosci Lett. 2018 Jan 1;662:181-184. doi: 10.1016/j.neulet.2017.09.029. Epub 2017 Sep 14. Neurosci Lett. 2018. PMID: 28917980

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