Shen L - Search Results

1

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.

Tang BS, Zhao GH, Luo W, Xia K, Cai F, Pan Q, Zhang RX, Zhang FF, Liu XM, Chen B, Zhang C, Shen L, Jiang H, Long ZG, Dai HP. Tang BS, et al. Among authors: shen l. Hum Genet. 2005 Feb;116(3):222-4. doi: 10.1007/s00439-004-1218-3. Epub 2004 Nov 23. Hum Genet. 2005. PMID: 15565283

2

[A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions].

Li HY, Tang BS, Zhang AM, Cao QH, Meng GL, Jiang H, Shen L. Li HY, et al. Among authors: shen l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Dec;20(6):482-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14669214 Chinese.

3

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H. Tang B, et al. Among authors: shen l. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

4

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

Tang BS, Luo W, Xia K, Xiao JF, Jiang H, Shen L, Tang JG, Zhao GH, Cai F, Pan Q, Dai HP, Yang QD, Xia JH, Evgrafov OV. Tang BS, et al. Among authors: shen l. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

5

A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family.

Tang B, Li H, Xia K, Jiang H, Pan Q, Shen L, Long Z, Zhao G, Cai F. Tang B, et al. Among authors: shen l. J Neurol Sci. 2004 Jun 15;221(1-2):31-4. doi: 10.1016/j.jns.2004.03.001. J Neurol Sci. 2004. PMID: 15178210

6

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

7

[Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].

Jiang H, Tang B, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K. Jiang H, et al. Among authors: shen l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):1-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696468 Chinese.

8

Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease.

Zhang RX, Luo W, Zi XH, Xia K, Cai F, Xiao JF, Zhao GH, Zhang FF, Shen L, Jiang H, Tang BS. Zhang RX, et al. Among authors: shen l. Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):68-71. Beijing Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 15719046 Free article.

9

[ATM gene mutations in Chinese patients with ataxia telangiectasia].

Jiang H, Tang B, Hu Z, Xia K, Xu B, Tang J, Shen L. Jiang H, et al. Among authors: shen l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):121-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793768 Chinese.

10

Research on screening and identification of proteins interacting with ataxin-3.

Shen L, Tang JG, Tang BS, Jiang H, Zhao GH, Xia K, Zhang YH, Cai F, Tan LM, Pan Q. Shen L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):242-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952105

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