Long Z - Search Results

1

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

2

FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patients.

Luo LZ, Xu Q, Guo JF, Wang L, Shi CH, Wei JH, Long ZG, Pan Q, Tang BS, Xia K, Yan XX. Luo LZ, et al. Neurosci Lett. 2010 Sep 27;482(2):86-9. doi: 10.1016/j.neulet.2010.06.083. Epub 2010 Jul 14. Neurosci Lett. 2010. PMID: 20603184

3

[Mutation analysis of ganglioside-induced differentiation associated protein-1 gene in Chinese Charcot-Marie-Tooth disease].

Zhang RX, Tang BS, Zi XH, Luo W, Xia K, Pan Q, Long ZG, Hu ZM, Li XB. Zhang RX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):207-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192818 Chinese.

4

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: long z. 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

5

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X. Zhang Y, et al. Among authors: long z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):189-91. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793782 Chinese.

6

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia.

Jiang H, Tang B, Xia K, Hu Z, Shen L, Tang J, Zhao G, Zhang Y, Cai F, Pan Q, Long Z, Wang G, Dai H. Jiang H, et al. Among authors: long z. J Neurol Sci. 2006 Feb 15;241(1-2):1-6. doi: 10.1016/j.jns.2005.09.001. Epub 2005 Dec 27. J Neurol Sci. 2006. PMID: 16380133

7

Molecular analysis of SLC26A4 gene in a Chinese deafness family.

Hu H, Liang DS, Wu LQ, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):376-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086271

8

[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6].

Zhang YH, Tang BS, Guo JF, Xia K, Xu B, Cai F, Deng HX, Yan XX, Chen T, Cao L, Pan Q, Long ZG. Zhang YH, et al. Zhonghua Yi Xue Za Zhi. 2005 Jun 15;85(22):1538-41. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16179113 Chinese.

9

[Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation].

Hu H, Wu LQ, Liang DS, Feng Y, Cai F, Xia K, Pan Q, Long ZG, Dai HP, Xia JH. Hu H, et al. Zhonghua Fu Chan Ke Za Zhi. 2005 Sep;40(9):591-4. Zhonghua Fu Chan Ke Za Zhi. 2005. PMID: 16202311 Chinese.

10

[A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses].

Xie ZG, Hu ZM, Pan Q, Zhang RF, Liang DS, Wu LQ, Long ZG, Dai HP, Xia K, Xia JH. Xie ZG, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):147-50. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604483 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,839 results

Search Page

Filters