Shi Y - Search Results

1

Gene mutations in a Han Chinese Alzheimer's disease cohort.

Ma L, Zhang J, Shi Y, Wang W, Ren Z, Xia M, Zhang Y, Yang M. Ma L, et al. Among authors: shi y. Brain Behav. 2019 Jan;9(1):e01180. doi: 10.1002/brb3.1180. Epub 2018 Dec 14. Brain Behav. 2019. PMID: 30549411 Free PMC article.

2

Phenotypic variation of Val1589Met mutation in a four-generation Chinese pedigree with mild paramyotonia congenitia: case report.

Xu C, Qi J, Shi Y, Feng Y, Zang W, Zhang J. Xu C, et al. Among authors: shi y. Int J Clin Exp Pathol. 2015 Jan 1;8(1):1050-6. eCollection 2015. Int J Clin Exp Pathol. 2015. PMID: 25755818 Free PMC article.

3

Probable novel PSEN2 Pro123Leu mutation in a Chinese Han family of Alzheimer's disease.

Xia M, Chen S, Shi Y, Huang Y, Xu J, Zhao T, He S, Wu Y, Xu C, Zang W, Zhang J. Xia M, et al. Among authors: shi y. Neurobiol Aging. 2015 Dec;36(12):3334.e13-3334.e18. doi: 10.1016/j.neurobiolaging.2015.09.003. Epub 2015 Sep 8. Neurobiol Aging. 2015. PMID: 26422362

4

[Anti-N-methyl-D-aspartate receptor encephalitis:clinical analysis of 11 cases].

Wu Y, Shi Y, Zhang M, Liu J, Zhou Y, Huang Y, Liu H, Ma M, Zhang J. Wu Y, et al. Among authors: shi y. Zhonghua Yi Xue Za Zhi. 2015 Sep 15;95(35):2857-60. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26815189 Chinese.

5

Anti-N-methyl-D-aspartate receptor encephalitis with lung adenocarcinoma.

Wu YY, He XJ, Zhang ML, Shi YY, Zhang JW. Wu YY, et al. Neurol Sci. 2016 Sep;37(9):1573-5. doi: 10.1007/s10072-016-2563-4. Epub 2016 Mar 30. Neurol Sci. 2016. PMID: 27028879 No abstract available.

6

A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like.

Chen Z, Ren Z, Mei W, Ma Q, Shi Y, Zhang Y, Li S, Xiang L, Zhang J. Chen Z, et al. Among authors: shi y. BMC Med Genet. 2017 Jun 5;18(1):63. doi: 10.1186/s12881-017-0424-5. BMC Med Genet. 2017. PMID: 28583108 Free PMC article.

7

[CADASIL with clinical manifestations of baldness, lumbago and Parkinson's symptoms].

Ren Z, Chen S, Shi Y, Zhang Y, Wang W, Chen Z, Xia M, Shi X, Zhang J. Ren Z, et al. Among authors: shi y, shi x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):821-825. doi: 10.3760/cma.j.issn.1003-9406.2017.06.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188608 Chinese.

8

Novel compound heterozygous mutations in the PARK2 gene identified in a Chinese pedigree with early-onset Parkinson's disease.

Shi Y, Kawakami H, Zang W, Li G, Zhang J, Xu C. Shi Y, et al. Brain Behav. 2017 Dec 19;8(1):e00901. doi: 10.1002/brb3.901. eCollection 2018 Jan. Brain Behav. 2017. PMID: 29568695 Free PMC article.

9

A novel KIAA0196 mutation in a Chinese patient with spastic paraplegia 8: A case report.

Ma L, Shi Y, Chen Z, Li S, Qin W, Zhang J. Ma L, et al. Among authors: shi y. Medicine (Baltimore). 2018 May;97(20):e10760. doi: 10.1097/MD.0000000000010760. Medicine (Baltimore). 2018. PMID: 29768361 Free PMC article.

10

A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosis.

Ma L, Shi Y, Chen Z, Li S, Zhang J. Ma L, et al. Among authors: shi y. Brain Behav. 2018 Sep;8(9):e01066. doi: 10.1002/brb3.1066. Epub 2018 Jul 27. Brain Behav. 2018. PMID: 30052327 Free PMC article.

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