Chen Y - Search Results

1

Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor.

Wu H, Lu X, Cen Z, Xie F, Zheng X, Chen Y, Luo W. Wu H, et al. Among authors: chen y. Neurosci Lett. 2016 Nov 10;634:104-106. doi: 10.1016/j.neulet.2016.10.005. Epub 2016 Oct 4. Neurosci Lett. 2016. PMID: 27717833

2

Genetic analysis of the TMEM230 gene in Chinese patients with familial Parkinson disease.

Wu H, Zheng X, Cen Z, Xie F, Chen Y, Lu X, Luo W. Wu H, et al. Among authors: chen y. Parkinsonism Relat Disord. 2017 Mar;36:105-106. doi: 10.1016/j.parkreldis.2016.12.021. Epub 2016 Dec 22. Parkinsonism Relat Disord. 2017. PMID: 28038866 No abstract available.

3

Dramatic response to pyridoxine in a girl with absence epilepsy with ataxia caused by a de novo CACNA1A mutation.

Du X, Chen Y, Zhao Y, Luo W, Cen Z, Hao W. Du X, et al. Among authors: chen y. Seizure. 2017 Feb;45:189-191. doi: 10.1016/j.seizure.2016.12.020. Epub 2017 Jan 3. Seizure. 2017. PMID: 28088730 Free article. No abstract available.

4

[A pedigree with dentatorubralpallidolyysian atrophy].

Lu X, Xie F, Cen Z, Wu H, Zheng X, Chen Y, Luo W. Lu X, et al. Among authors: chen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):934-935. doi: 10.3760/cma.j.issn.1003-9406.2017.06.035. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188634 Chinese. No abstract available.

5

Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.

Cen Z, Jiang Z, Chen Y, Zheng X, Xie F, Yang X, Lu X, Ouyang Z, Wu H, Chen S, Yin H, Qiu X, Wang S, Ding M, Tang Y, Yu F, Li C, Wang T, Ishiura H, Tsuji S, Jiao C, Liu C, Xiao J, Luo W. Cen Z, et al. Among authors: chen s, chen y. Brain. 2018 Aug 1;141(8):2280-2288. doi: 10.1093/brain/awy160. Brain. 2018. PMID: 29939203

6

[Genetic study of a Parkinson's disease pedigree caused by compound heterozygous mutations in PARK2 gene].

Chen M, Cen Z, Chen Y, Zheng X, Xie F, Chen S, Luo W. Chen M, et al. Among authors: chen s, chen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):815-818. doi: 10.3760/cma.j.issn.1003-9406.2018.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512153 Chinese.

7

Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.

Chen Y, Fu F, Chen S, Cen Z, Tang H, Huang J, Xie F, Zheng X, Yang D, Wang H, Huang X, Zhang Y, Zhou Y, Liu JY, Luo W. Chen Y, et al. Among authors: chen s. Mov Disord. 2019 Feb;34(2):291-297. doi: 10.1002/mds.27582. Epub 2018 Dec 27. Mov Disord. 2019. PMID: 30589467

8

A Novel Homozygous CAPN1 Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic Paraplegia.

Chen Y, Cen Z, Zheng X, Xie F, Chen S, Luo W. Chen Y, et al. Among authors: chen s. J Clin Neurol. 2019 Apr;15(2):271-272. doi: 10.3988/jcn.2019.15.2.271. J Clin Neurol. 2019. PMID: 30938113 Free PMC article. No abstract available.

9

LRP10 in autosomal-dominant Parkinson's disease.

Chen Y, Cen Z, Zheng X, Pan Q, Chen X, Zhu L, Chen S, Wu H, Xie F, Wang H, Yang D, Wang L, Zhang B, Luo W. Chen Y, et al. Among authors: chen s, chen x. Mov Disord. 2019 Jun;34(6):912-916. doi: 10.1002/mds.27693. Epub 2019 Apr 9. Mov Disord. 2019. PMID: 30964957

10

Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China.

Chen S, Cen Z, Fu F, Chen Y, Chen X, Yang D, Wang H, Wu H, Zheng X, Xie F, Ouyang Z, Tang W, Zhang S, Yin L, Zhang Y, Meng P, Zhu X, Zhang H, Jiang F, Zhang K, He J, Zhang D, Ming H, Song D, Zhou Z, Luo Y, Gu Q, Su Y, Wu X, Tang H, Wu C, Chen W, Liu JY, Luo W; Chinese PFBC Study Group. Chen S, et al. Among authors: chen w, chen x, chen y. Parkinsonism Relat Disord. 2019 Jul;64:211-219. doi: 10.1016/j.parkreldis.2019.04.009. Epub 2019 Apr 11. Parkinsonism Relat Disord. 2019. PMID: 31003906

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