Tang B - Search Results

1

[X-linked recessive Charcot-Marie-Tooth disease and Cx32 gene mutation].

Luo W, Tang B, Xiao J. Luo W, et al. Among authors: tang b. Zhonghua Nei Ke Za Zhi. 2001 Aug;40(8):543-5. Zhonghua Nei Ke Za Zhi. 2001. PMID: 11718056 Chinese.

2

[PCR in the gene diagnosis of Charcot-Marie-Tooth disease].

Xiao J, Tang B, Xia J. Xiao J, et al. Among authors: tang b. Zhonghua Yi Xue Za Zhi. 2001 Feb 10;81(3):138-41. Zhonghua Yi Xue Za Zhi. 2001. PMID: 11798863 Chinese.

3

[CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].

Tang B, Xia J, Wang D, Tang X, Shen L, Liu C, Dai H, Yan X, Pan Q, Xiao J, Zhang B, Ou Y. Tang B, et al. Among authors: tang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999 Oct;16(5):281-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999. PMID: 10514531 Chinese.

4

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.

Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ. Xia JH, et al. Among authors: tang bs. Nat Genet. 1998 Dec;20(4):370-3. doi: 10.1038/3845. Nat Genet. 1998. PMID: 9843210

5

Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.

Xia JH, Yang YF, Deng H, Tang BS, Tang DS, He YG, Xia K, Chen SX, Li YX, Pan Q, Long ZG, Dai HP, Liao XD, Xiao JF, Liu ZR, Lu CY, Yu KP, Deng HX. Xia JH, et al. Among authors: tang bs, tang ds. J Invest Dermatol. 2000 Jun;114(6):1071-4. doi: 10.1046/j.1523-1747.2000.00978.x. J Invest Dermatol. 2000. PMID: 10844547 Free article.

6

[Analysis of the parkin gene deletion mutations in Chinese patients with Parkinson's disease].

Tang B, Liu S, Yan X, Shen L, Jiang H, Yang Q, Ouyang S. Tang B, et al. Zhonghua Nei Ke Za Zhi. 2001 Dec;40(12):799-801. Zhonghua Nei Ke Za Zhi. 2001. PMID: 16206665 Chinese.

7

Phenotypes and cellular effects of GJB1 mutations causing CMT1X in a cohort of 226 Chinese CMT families.

Liu L, Li XB, Hu ZHM, Zi XH, Zhao X, Xie YZ, Huang SHX, Xia K, Tang BS, Zhang RX. Liu L, et al. Among authors: tang bs. Clin Genet. 2017 Jun;91(6):881-891. doi: 10.1111/cge.12913. Epub 2017 Mar 8. Clin Genet. 2017. PMID: 27804109

8

[A novel mutation of SCN4A gene causes hypokalemic periodic paralysis in a Chinese family].

Li HY, Zhou XL, Guo JF, Tang BS, Fu YJ, Sun JY. Li HY, et al. Among authors: tang bs. Zhonghua Yi Xue Za Zhi. 2020 Dec 8;100(45):3622-3625. doi: 10.3760/cma.j.cn112137-20200421-01265. Zhonghua Yi Xue Za Zhi. 2020. PMID: 33333687 Chinese.

9

[SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].

Tang B, Wang D, Xia J. Tang B, et al. Zhonghua Yi Xue Za Zhi. 1997 Nov;77(11):819-22. Zhonghua Yi Xue Za Zhi. 1997. PMID: 9772474 Chinese.

10

[Experts consensus on the management of delirium in critically ill patients].

Tang B, Wang XT, Chen WJ, Zhu SH, Chao YG, Zhu B, He W, Wang B, Cao FF, Liu YJ, Fan XJ, Yang H, Xu QH, Zhang H, Gong RC, Chai WZ, Zhang HM, Shi GZ, Li LH, Huang QB, Zhang LN, Yin MG, Shang XL, Wang XM, Tian F, Liu LX, Zhu R, Wu J, Wu YQ, Li CL, Zong Y, Hu JT, Liu J, Zhai Q, Deng LJ, Deng YY, Liu DW; Chinese Critical Hypothermia-Sedation Therapy Study Group. Tang B, et al. Zhonghua Nei Ke Za Zhi. 2019 Feb 1;58(2):108-118. doi: 10.3760/cma.j.issn.0578-1426.2019.02.007. Zhonghua Nei Ke Za Zhi. 2019. PMID: 30704197 Chinese.

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