Xiao JF - Search Results

1

[The characteristics of gene mutations in Chinese patients with Charcot-Marie-Tooth disease].

Zhang FF, Tang BS, Zhao GH, Luo W, Xia K, Liu XM, Xiao JF, Zhang RX, Chen B, Hang C, Pan Q, Cai F, Guo P. Zhang FF, et al. Among authors: xiao jf. Zhonghua Yi Xue Za Zhi. 2005 Jul 13;85(26):1809-12. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16253183 Chinese.

2

[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. Among authors: xiao jf. 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.

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: xiao jf. 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

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: xiao jf. 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.

5

[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.

6

[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.

7

[The clinical and pathologic features of Charcot-Marie-Tooth disease].

Xiao B, Xie J, Yang X, Wu Z, Xiao J, Li J. Xiao B, et al. Zhonghua Nei Ke Za Zhi. 2002 Nov;41(11):736-8. Zhonghua Nei Ke Za Zhi. 2002. PMID: 12485517 Chinese.

8

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: xiao jf. 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.

9

Novel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysis.

Xie F, Cen ZD, Xiao JF, Luo W. Xie F, et al. Among authors: xiao jf. Neurol Sci. 2015 Jul;36(7):1279-80. doi: 10.1007/s10072-014-2018-8. Epub 2014 Nov 30. Neurol Sci. 2015. PMID: 25433428 No abstract available.

10

Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.

Cen ZD, Xie F, Xiao JF, Luo W. Cen ZD, et al. Among authors: xiao jf. Seizure. 2016 Jan;34:83-9. doi: 10.1016/j.seizure.2015.12.004. Epub 2015 Dec 15. Seizure. 2016. PMID: 26751243 Free article. Review.

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