Tang B - Search Results

1

Clinical Heterogeneity Among LRRK2 Variants in Parkinson's Disease: A Meta-Analysis.

Shu L, Zhang Y, Pan H, Xu Q, Guo J, Tang B, Sun Q. Shu L, et al. Among authors: tang b. Front Aging Neurosci. 2018 Sep 19;10:283. doi: 10.3389/fnagi.2018.00283. eCollection 2018. Front Aging Neurosci. 2018. PMID: 30283330 Free PMC article.

2

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. Mov Disord. 2005 Jul;20(7):819-21. doi: 10.1002/mds.20408. Mov Disord. 2005. PMID: 15747360 Free PMC article.

3

[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: tang b, tang j. 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.

4

[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.

5

[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.

6

[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.

7

[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.

8

[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.

9

[Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR].

Guo JF, Tang BS, Li J, Zhang YH, Zhang XW, Chen T, Xia K, Yan XX, Cao L, Cai F, Pan Q, Shen L, Jiang H. Guo JF, et al. Zhonghua Yi Xue Za Zhi. 2006 Jun 6;86(21):1447-9. Zhonghua Yi Xue Za Zhi. 2006. PMID: 16842693 Chinese.

10

[Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].

Li HY, Tang BS, Yan XX, Guo JF, Shen L, Song YM, Jiang H, Xia K, Xie ZG, Yang QA. Li HY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Aug;23(4):374-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16883520 Chinese.

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