Zhao GH - Search Results

1

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: zhao gh. 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.

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

[Mutation analysis of neurofilament-light gene in Chinese Charcot-Marie-Tooth disease].

Luo W, Tang B, Zhao G, Li Q, Xiao J, Yang Q, Xia J. Luo W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):169-70. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12673592 Chinese.

4

[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. 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.

5

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

6

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

7

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. 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

8

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

9

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

10

[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: zhao gh. 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.

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