Yin X - Search Results

1

Locus coeruleus degeneration and cerebellar gray matter changes in essential tremor.

Lv D, Zhou C, Pu J, Lu J, Zhao G, Gu L, Guan X, Guo T, Xu X, Zhang M, Tian J, Yin X, Zhang B, Zhao G, Yan Y. Lv D, et al. Among authors: yin x. J Neurol. 2023 Feb;270(2):780-787. doi: 10.1007/s00415-022-11409-z. Epub 2022 Oct 4. J Neurol. 2023. PMID: 36194299

2

[Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma].

Zhang BR, Yin XZ, Xia K, Ding MP, Hu ZM, Zheng M, Liu ZR, Xia JH. Zhang BR, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):570-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583984 Chinese.

3

[IT15 gene analysis in two pedigrees of Huntington's disease].

Zhang BR, Song F, Yin XZ, Xia K, Tian J, Huang JZ, Xia JH. Zhang BR, et al. Yi Chuan. 2006 Nov;28(11):1345-9. doi: 10.1360/yc-006-1345. Yi Chuan. 2006. PMID: 17098699 Chinese.

4

[Pathological features and gene mutation analysis in two pedigrees of diffuse palmoplantar keratoderma].

Yin XZ, Zhang BR, Ding MP, Zhang H, Xia K, Hu ZM. Yin XZ, et al. Yi Chuan. 2007 Mar;29(3):301-5. doi: 10.1360/yc-007-0301. Yi Chuan. 2007. PMID: 17369150 Chinese.

5

[The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].

Yin XZ, Zhang BR, Wu DW, Tian J, Zhang H. Yin XZ, et al. Yi Chuan. 2007 Jun;29(6):688-92. doi: 10.1360/yc-007-0688. Yi Chuan. 2007. PMID: 17650485 Chinese.

6

Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus.

Zhang B, Liu Z, Zhao G, Xie X, Yin X, Hu Z, Xu S, Li Q, Song F, Tian J, Luo W, Ding M, Yin J, Xia K, Xia J. Zhang B, et al. Among authors: yin j, yin x. Mol Vis. 2007 Sep 13;13:1674-9. Mol Vis. 2007. PMID: 17893669

7

Report of two Chinese families and a review of Mainland Chinese CADASIL patients.

Yin XZ, Ding MP, Zhang BR, Liu JR, Zhang L, Wang PZ, Zhou FY, Zhao GH. Yin XZ, et al. J Neurol Sci. 2009 Apr 15;279(1-2):88-92. doi: 10.1016/j.jns.2008.12.011. Epub 2009 Jan 23. J Neurol Sci. 2009. PMID: 19167727 Review.

8

Mutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in China.

Zhang BR, Hu ZX, Yin XZ, Cai M, Zhao GH, Liu ZR, Luo W. Zhang BR, et al. Neurosci Lett. 2010 Jun 14;477(1):19-22. doi: 10.1016/j.neulet.2010.04.026. Epub 2010 Apr 23. Neurosci Lett. 2010. PMID: 20399249

9

Clinical features and Cu/Zn superoxide dismutase gene mutations in two mainland Chinese families with amyotrophic lateral sclerosis.

Zhao G, Yin X, Wu D, Mao S, Yin H, Zhang B. Zhao G, et al. Among authors: yin x, yin h. Int J Neurosci. 2011 Apr;121(4):191-5. doi: 10.3109/00207454.2010.542841. Int J Neurosci. 2011. PMID: 21329474

10

Essential sequence of the N-terminal cytoplasmic localization-related domain of huntingtin and its effect on huntingtin aggregates.

Yan Y, Peng D, Tian J, Chi J, Tan J, Yin X, Pu J, Xia K, Zhang B. Yan Y, et al. Among authors: yin x. Sci China Life Sci. 2011 Apr;54(4):342-50. doi: 10.1007/s11427-011-4151-4. Epub 2011 Mar 8. Sci China Life Sci. 2011. PMID: 21509658

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