Tang BS - Search Results

1

Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China.

Liu ZH, Guo JF, Wang YQ, Li K, Sun QY, Xu Q, Yan XX, Xu CS, Tang BS. Liu ZH, et al. Among authors: tang bs. Neurobiol Aging. 2015 Mar;36(3):1600.e9-11. doi: 10.1016/j.neurobiolaging.2014.12.012. Epub 2014 Dec 13. Neurobiol Aging. 2015. PMID: 25559334

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: tang bs. 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. Chin Med J (Engl). 2004 Jul;117(7):1002-5. Chin Med J (Engl). 2004. PMID: 15265372

5

Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.

Zhang YH, Tang BS, Zhao AL, Xia K, Long ZG, Guo JF, Westaway SK, Hayflick SJ. Zhang YH, et al. Among authors: tang bs. Mov Disord. 2005 Jul;20(7):819-21. doi: 10.1002/mds.20408. Mov Disord. 2005. PMID: 15747360 Free PMC article.

6

[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.

7

[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: tang bs. Zhonghua Nei Ke Za Zhi. 2005 May;44(5):360-2. Zhonghua Nei Ke Za Zhi. 2005. PMID: 16009007 Chinese.

8

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: tang bs. 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

9

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

10

[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: tang bs. 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.

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