Luo H - Search Results

1

CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61I.

Mao C, Wang H, Luo H, Zhang S, Xu H, Zhang S, Rosenblum J, Wang Z, Zhang Q, Tang M, Shepard MJ, Wang X, Wang Y, Zhuang Z, Shi C, Xu Y. Mao C, et al. Among authors: luo h. Neurobiol Aging. 2019 Mar;75:38-41. doi: 10.1016/j.neurobiolaging.2018.10.020. Epub 2018 Oct 23. Neurobiol Aging. 2019. PMID: 30530185 Free PMC article.

2

A novel compound WISP3 mutation in a Chinese family with progressive pseudorheumatoid dysplasia.

Luo H, Shi C, Mao C, Jiang C, Bao D, Guo J, Du P, Wang Y, Liu Y, Liu X, Song B, Xu Y. Luo H, et al. Gene. 2015 Jun 10;564(1):35-8. doi: 10.1016/j.gene.2015.03.029. Epub 2015 Mar 17. Gene. 2015. PMID: 25794430

3

Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes.

Li YS, Mao CY, Shi CH, Song B, Wu J, Qin J, Ji Y, Niu HX, Luo HY, Shang DD, Sun SL, Xu YM. Li YS, et al. J Clin Neurosci. 2015 Jul;22(7):1150-4. doi: 10.1016/j.jocn.2015.01.014. Epub 2015 May 21. J Clin Neurosci. 2015. PMID: 26003865

4

Recessive hereditary motor and sensory neuropathy caused by IGHMBP2 gene mutation.

Shi CH, Song B, Luo HY, Mao CY, Shang DD, Cao Y, Sun SL, Wu J, Zhuang ZP, Xu YM. Shi CH, et al. Neurology. 2015 Jul 28;85(4):383-4. doi: 10.1212/WNL.0000000000001747. Epub 2015 Jul 1. Neurology. 2015. PMID: 26136520 Free PMC article. No abstract available.

5

MMACHC gene mutation in familial hypogonadism with neurological symptoms.

Shi C, Shang D, Sun S, Mao C, Qin J, Luo H, Shao M, Chen Z, Liu Y, Liu X, Song B, Xu Y. Shi C, et al. Among authors: luo h. Gene. 2015 Dec 15;574(2):380-4. doi: 10.1016/j.gene.2015.08.029. Epub 2015 Aug 14. Gene. 2015. PMID: 26283149

6

Plasma Homocysteine, Vitamin B12 and Folate Levels in Multiple System Atrophy: A Case-Control Study.

Zhang S, Shi C, Mao C, Song B, Hou H, Wu J, Liu X, Luo H, Sun S, Xu Y. Zhang S, et al. Among authors: luo h. PLoS One. 2015 Aug 20;10(8):e0136468. doi: 10.1371/journal.pone.0136468. eCollection 2015. PLoS One. 2015. PMID: 26291976 Free PMC article.

7

Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.

Mao CY, Yang J, Zhang SY, Luo HY, Song B, Liu YT, Wu J, Sun SL, Yang ZH, Du P, Wang YH, Shi CH, Xu YM. Mao CY, et al. Int J Neurosci. 2016 Dec;126(12):1071-6. doi: 10.3109/00207454.2015.1118628. Epub 2015 Dec 7. Int J Neurosci. 2016. PMID: 26643368

8

MC1R variants in Chinese Han patients with sporadic Parkinson's disease.

Shi CH, Wang H, Mao CY, Yang J, Song B, Liu YT, Yang ZH, Luo HY, Zhang SY, Wu J, Xu YM. Shi CH, et al. Among authors: luo hy. Neurobiol Aging. 2016 Jun;42:217.e5-6. doi: 10.1016/j.neurobiolaging.2016.02.026. Epub 2016 Mar 3. Neurobiol Aging. 2016. PMID: 27084066

9

Pseudo-dominant inheritance of a novel double GLA mutation associated with Fabry disease mimicking familial episodic pain.

Mao C, Luo H, Yang J, Qin J, Wang H, Song B, Sun S, Zhuang Z, Shi C, Xu Y. Mao C, et al. Among authors: luo h. Am J Med Genet A. 2016 Nov;170(11):3051-3053. doi: 10.1002/ajmg.a.37833. Epub 2016 Aug 17. Am J Med Genet A. 2016. PMID: 27531472 No abstract available.

10

SMPD1 variants in Chinese Han patients with sporadic Parkinson's disease.

Mao CY, Yang J, Wang H, Zhang SY, Yang ZH, Luo HY, Li F, Shi M, Liu YT, Zhuang ZP, Du P, Wang YH, Shi CH, Xu YM. Mao CY, et al. Among authors: luo hy. Parkinsonism Relat Disord. 2017 Jan;34:59-61. doi: 10.1016/j.parkreldis.2016.10.014. Epub 2016 Oct 19. Parkinsonism Relat Disord. 2017. PMID: 27814975

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

13,311 results

Search Page

Filters