Long ZG - Search Results

1

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. Among authors: long zg. 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

2

[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. Among authors: long zg. Zhonghua Yi Xue Za Zhi. 2005 Jun 15;85(22):1538-41. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16179113 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. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

4

[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. 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.

5

[Mutation screening of the dystrophin gene in 14 Chinese Duchenne/Becker muscular dystrophy patients without gross deletions].

Xue J, Zhu H, Wu L, Liang D, Pan Q, Long Z, Dai H, Xia K, Xia J. Xue J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):633-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065519 Chinese.

6

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. Among authors: long zg. 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

7

Analysis of PAX6 gene in a Chinese aniridia family.

Zhu HY, Wu LQ, Pan Q, Liang DS, Long ZG, Dai HP, Xia K, Xia JH. Zhu HY, et al. Among authors: long zg. Chin Med J (Engl). 2006 Aug 20;119(16):1400-2. Chin Med J (Engl). 2006. PMID: 16934188 No abstract available.

8

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.

Wang JL, Xiao B, Cui XX, Guo JF, Lei LF, Song XW, Shen L, Jiang H, Yan XX, Pan Q, Long ZG, Xia K, Tang BS. Wang JL, et al. Among authors: long zg. Mov Disord. 2009 Oct 15;24(13):2007-11. doi: 10.1002/mds.22727. Mov Disord. 2009. PMID: 19672991

9

[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. Among authors: long zg. 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.

10

Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.

Zhang YH, Tang BS, Zhao AL, Xia K, Long ZG, Guo JF, Westaway SK, Hayflick SJ. Zhang YH, et al. Among authors: long zg. Mov Disord. 2005 Jul;20(7):819-21. doi: 10.1002/mds.20408. Mov Disord. 2005. PMID: 15747360 Free PMC article.

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