Yan X - Search Results

1

The Chinese Parkinson's Disease Registry (CPDR): Study Design and Baseline Patient Characteristics.

Zhou X, Liu Z, Zhou X, Xiang Y, Zhou Z, Zhao Y, Pan H, Xu Q, Chen Y, Sun Q, Wu X, Tan H, Li B, Yuan K, Xie Y, Liao W, Hu S, Zhu J, Wu X, Li J, Wang C, Lei L, Tang J, Liu Y, Wu H, Huang W, Wang T, Xue Z, Wang P, Zhang Z, Xu P, Chen L, Wang Q, Wang X, Cheng O, Shen Y, Liu W, Ye M, You Y, Li J, Yan X, Guo J, Tang B; for Parkinson's Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC). Zhou X, et al. Among authors: yan x. Mov Disord. 2022 Jul;37(7):1335-1345. doi: 10.1002/mds.29037. Epub 2022 May 3. Mov Disord. 2022. PMID: 35503029

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. Among authors: yan x. 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. 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. Among authors: yan x. 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. Zhonghua Nei Ke Za Zhi. 2005 May;44(5):360-2. Zhonghua Nei Ke Za Zhi. 2005. PMID: 16009007 Chinese.

7

[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. Zhonghua Yi Xue Za Zhi. 2005 Jun 15;85(22):1538-41. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16179113 Chinese.

8

[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. 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.

9

[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. 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.

10

[Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism].

Guo JF, Tang BS, Zhang YH, Liu HJ, Yan XX, Chen T, Shen L, Jiang H, Xia K, Cai F, Pan Q. Guo JF, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Feb;23(1):70-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16456791 Chinese.

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