Zhang C - Search Results

1

Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.

Tang B, Liu X, Zhao G, Luo W, Xia K, Pan Q, Cai F, Hu Z, Zhang C, Chen B, Zhang F, Shen L, Zhang R, Jiang H. Tang B, et al. Among authors: zhang r, zhang c, zhang f. Arch Neurol. 2005 Aug;62(8):1201-7. doi: 10.1001/archneur.62.8.1201. Arch Neurol. 2005. PMID: 16087758

2

[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR].

Zhang FF, Tang BS, Shen Y, Zhao GH, Xia K, Zhao YQ, Chen B, Zhang C, Pan Q, Cai F, Liu XM, Luo W, Zhang RX, Guo P. Zhang FF, et al. Among authors: zhang rx, zhang c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):537-40. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215943 Chinese.

3

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: zhang rx, zhang c, zhang ff. Hum Genet. 2005 Feb;116(3):222-4. doi: 10.1007/s00439-004-1218-3. Epub 2004 Nov 23. Hum Genet. 2005. PMID: 15565283

4

Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.

Zhang FF, Tang BS, Zhao GH, Chen B, Zhang C, Luo W, Liu XM, Xia K, Cai F, Hu ZM, Yan XX, Zhang RX, Guo P. Zhang FF, et al. Among authors: zhang rx, zhang c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):361-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086267

5

[Mutation analysis of small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease].

Liu XM, Tang BS, Zhao GH, Xia K, Zhang FF, Pan Q, Cai F, Hu ZM, Zhang C, Chen B, Shen L, Zhang RX, Jiang H. Liu XM, et al. Among authors: zhang rx, zhang c, zhang ff. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):510-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215937 Chinese.

6

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

Sun SC, Ma D, Li MY, Zhang RX, Huang C, Huang HJ, Xie YZ, Wang ZJ, Liu J, Cai DC, Liu CX, Yang Q, Bao FX, Gong XL, Li JR, Hui Z, Wei XF, Zhong JM, Zhou WJ, Shang X, Zhang C, Liu XG, Tang BS, Xiong F, Xu XM. Sun SC, et al. Among authors: zhang rx, zhang c. Brain. 2019 Aug 1;142(8):2215-2229. doi: 10.1093/brain/awz151. Brain. 2019. PMID: 31199454

7

Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China.

Cao L, Huang X, Wang N, Wu Z, Zhang C, Gu W, Cong S, Ma J, Wei L, Deng Y, Fang Q, Niu Q, Wang J, Wang Z, Yin Y, Tian J, Tian S, Bi H, Jiang H, Liu X, Lü Y, Sun M, Wu J, Xu E, Chen T, Chen T, Chen X, Li W, Li S, Li Q, Song X, Tang Y, Yang P, Yang Y, Zhang M, Zhang X, Zhang Y, Zhang R, Ouyang Y, Yu J, Hu Q, Ke Q, Yao Y, Zhao Z, Zhao X, Zhao G, Liang F, Cheng N, Han J, Peng R, Chen S, Tang B. Cao L, et al. Among authors: zhang m, zhang r, zhang c, zhang x, zhang y. Transl Neurodegener. 2021 Feb 16;10(1):7. doi: 10.1186/s40035-021-00231-8. Transl Neurodegener. 2021. PMID: 33588936 Free PMC article. Review.

8

Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families.

Chen S, Song C, Guo H, Xu P, Huang W, Zhou Y, Sun J, Li CX, Du Y, Li X, Liu Z, Geng D, Maxwell PH, Zhang C, Wang Y. Chen S, et al. Among authors: zhang c. Hum Mutat. 2005 Feb;25(2):135-41. doi: 10.1002/humu.20126. Hum Mutat. 2005. PMID: 15643603

9

Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.

He R, Li H, Sun Y, Chen M, Wang L, Zhu Y, Zhang C. He R, et al. Among authors: zhang c. BMC Neurol. 2020 Mar 2;20(1):72. doi: 10.1186/s12883-020-01660-0. BMC Neurol. 2020. PMID: 32122318 Free PMC article.

10

Congenital muscular dystrophies in China.

Ge L, Zhang C, Wang Z, Chan SHS, Zhu W, Han C, Zhang X, Zheng H, Wu L, Jin B, Shan J, Mao B, Zhong J, Peng X, Cheng Y, Hu J, Sun Y, Lu J, Hua Y, Zhu S, Wei C, Wang S, Jiao H, Yang H, Fu X, Fan Y, Chang X, Wang S, Bao X, Zhang Y, Wang J, Wu Y, Jiang Y, Yuan Y, Rutkowski A, Bönnemann CG, Wei W, Wu X, Xiong H. Ge L, et al. Among authors: zhang c, zhang x, zhang y. Clin Genet. 2019 Sep;96(3):207-215. doi: 10.1111/cge.13560. Epub 2019 Jun 6. Clin Genet. 2019. PMID: 31066047

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