Xia K - Search Results

1

Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis.

Wei L, Tian Y, Chen Y, Wei Q, Chen F, Cao B, Wu Y, Zhao B, Chen X, Xie C, Xi C, Yu X, Wang J, Lv X, Du J, Wang Y, Shen L, Wang X, Shen B, Guo Q, Guo L, Xia K, Xie P, Zhang X, Zuo X, Shang H, Wang K. Wei L, et al. Among authors: xia k. Neurol Genet. 2019 Nov 8;5(6):e375. doi: 10.1212/NXG.0000000000000375. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 31872054 Free PMC article.

2

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: xia k. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

3

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: xia k, xia jh. Hum Genet. 2004 May;114(6):527-33. doi: 10.1007/s00439-004-1102-1. Epub 2004 Mar 12. Hum Genet. 2004. PMID: 15021985

4

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: xia k. Hum Genet. 2005 Feb;116(3):222-4. doi: 10.1007/s00439-004-1218-3. Epub 2004 Nov 23. Hum Genet. 2005. PMID: 15565283

5

[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: xia k. 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.

6

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: xia k. 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.

7

[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: xia k. 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.

8

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. Among authors: xia k. 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

9

Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.

Jiang H, Tang B, Xia K, Zhou Y, Xu B, Zhao G, Li H, Shen L, Pan Q, Cai F. Jiang H, et al. Among authors: xia k. J Neurol Sci. 2005 Sep 15;236(1-2):25-9. doi: 10.1016/j.jns.2005.04.009. J Neurol Sci. 2005. PMID: 15979648

10

Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.

Jiang H, Tang BS, Xu B, Zhao GH, Shen L, Tang JG, Li QH, Xia K. Jiang H, et al. Among authors: xia k. Chin Med J (Engl). 2005 May 20;118(10):837-43. Chin Med J (Engl). 2005. PMID: 15989765

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