Yan XX - Search Results

1

PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.

Zhao YW, Pan HX, Zeng Q, Fang ZH, Liu ZH, Wang Y, Jiang L, He R, Zhou X, Zhou YJ, Xu Q, Sun QY, Li B, Zhao G, Yang Y, Hu YC, Chen YS, Du J, Lei LF, Zhang HN, Wang CY, Yan XX, Shen L, Jiang H, Li JC, Tang BS, Tan JQ, Guo JF. Zhao YW, et al. Among authors: yan xx. Brain. 2021 Apr 12;144(3):e25. doi: 10.1093/brain/awaa391. Brain. 2021. PMID: 33793763 No abstract available.

2

[A new mutation in the connexin 32 gene of a Chinese family with Charcot-Marie-Tooth disease associated with central conduction slowing].

Luo W, Tang B, Zhao G, Xia K, Yang Y, Xiao J, Yan X, Xia J. Luo W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Oct;19(5):367-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12362307 Chinese.

3

[Spastin gene mutation in Chinese patients with hereditary spastic paraplegia].

Zhao GH, Tang BS, Luo W, Xia K, Zhuang MY, Kong FB, Yan XX, Deng HX, Xiao JF, Xia JH. Zhao GH, et al. Among authors: yan xx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Jun;20(3):177-80. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12778437 Chinese.

4

Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases.

Tang BS, Chen X, Zhao GH, Shen L, Yan XX, Jiang H, Luo W. Tang BS, et al. Among authors: yan xx. Chin Med J (Engl). 2004 Jul;117(7):1002-5. Chin Med J (Engl). 2004. PMID: 15265372

5

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X. Zhang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):189-91. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793782 Chinese.

6

[The clinical and genetic characteristics of autosomal recessive juvenile Parkinsonism in a Chinese family].

Shen YW, Tang BS, Yan XX, Zhang YH, Guo JF, Jiang H. Shen YW, et al. Among authors: yan xx. Zhonghua Nei Ke Za Zhi. 2005 May;44(5):360-2. Zhonghua Nei Ke Za Zhi. 2005. PMID: 16009007 Chinese.

7

Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.

Zhang FF, Tang BS, Zhao GH, Chen B, Zhang C, Luo W, Liu XM, Xia K, Cai F, Hu ZM, Yan XX, Zhang RX, Guo P. Zhang FF, et al. Among authors: yan xx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):361-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086267

8

[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6].

Zhang YH, Tang BS, Guo JF, Xia K, Xu B, Cai F, Deng HX, Yan XX, Chen T, Cao L, Pan Q, Long ZG. Zhang YH, et al. Among authors: yan xx. Zhonghua Yi Xue Za Zhi. 2005 Jun 15;85(22):1538-41. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16179113 Chinese.

9

[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].

Guo JF, Tang BS, Zhang YH, Xia K, Cai F, Pan Q, Shen L, Jiang H, Zhao GH, Yan XX, Cao L. Guo JF, et al. Among authors: yan xx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):641-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331561 Chinese.

10

[The wild-type alpha-synuclein over-expression to induce the protein aberrant aggregation of alpha-synuclein in HEK293 cells in vitro].

Chen T, Tang BS, Liao XP, Yan XX, Zhang RX, Zhang YH, Tang JG, Cao L, Guo JF, Li J. Chen T, et al. Among authors: yan xx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Feb;23(1):19-22. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16456779 Chinese.

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