Cao L - Search Results

1

Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders.

Zhang C, Zhan FX, Tian WT, Xu YQ, Zhu ZY, Wang Y, Song XW, Cao L. Zhang C, et al. Among authors: cao l. Clin Neurol Neurosurg. 2019 Feb;177:92-96. doi: 10.1016/j.clineuro.2019.01.004. Epub 2019 Jan 7. Clin Neurol Neurosurg. 2019. PMID: 30640048 Review.

2

[Clinical features and treatment of giant cell arteritis in Chinese, a prospective study].

Hu Z, Yang Q, Li J, Zeng S, Wu X, Cao L, Yang L, Song X. Hu Z, et al. Among authors: cao l. Zhonghua Yi Xue Za Zhi. 2002 Apr 10;82(7):453-5. Zhonghua Yi Xue Za Zhi. 2002. PMID: 12133513 Chinese.

3

Mutations of SCN4A gene cause different diseases: 2 case reports and literature review.

Liu XL, Huang XJ, Luan XH, Zhou HY, Wang T, Wang JY, Chen SD, Tang HD, Cao L. Liu XL, et al. Among authors: cao l. Channels (Austin). 2015;9(2):82-7. doi: 10.1080/19336950.2015.1012945. Channels (Austin). 2015. PMID: 25839108 Free PMC article. Review.

4

Novel ATM mutations with ataxia-telangiectasia.

Liu XL, Wang T, Huang XJ, Zhou HY, Luan XH, Shen JY, Chen SD, Cao L. Liu XL, et al. Among authors: cao l. Neurosci Lett. 2016 Jan 12;611:112-5. doi: 10.1016/j.neulet.2015.11.036. Epub 2015 Nov 25. Neurosci Lett. 2016. PMID: 26628246

5

Limb-girdle congenital myasthenic syndrome in a Chinese family with novel mutations in MUSK gene and literature review.

Luan X, Tian W, Cao L. Luan X, et al. Among authors: cao l. Clin Neurol Neurosurg. 2016 Nov;150:41-45. doi: 10.1016/j.clineuro.2016.08.021. Epub 2016 Aug 22. Clin Neurol Neurosurg. 2016. PMID: 27588369 Review.

6

Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18.

Tian WT, Shen JY, Liu XL, Wang T, Luan XH, Zhou HY, Chen SD, Huang XJ, Cao L. Tian WT, et al. Among authors: cao l. Chin Med J (Engl). 2016 Nov 20;129(22):2759-2761. doi: 10.4103/0366-6999.193444. Chin Med J (Engl). 2016. PMID: 27824013 Free PMC article. No abstract available.

7

Depression, anxiety, and quality of life in paroxysmal kinesigenic dyskinesia patients.

Tian WT, Huang XJ, Liu XL, Shen JY, Liang GL, Zhu CX, Tang WG, Chen SD, Song YY, Cao L. Tian WT, et al. Among authors: cao l. Chin Med J (Engl). 2017 Sep 5;130(17):2088-2094. doi: 10.4103/0366-6999.213431. Chin Med J (Engl). 2017. PMID: 28836553 Free PMC article.

8

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS. Yin XM, et al. Among authors: cao l. Hum Mol Genet. 2018 Feb 15;27(4):625-637. doi: 10.1093/hmg/ddx430. Hum Mol Genet. 2018. PMID: 29294000

9

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS. Yin XM, et al. Among authors: cao l. Hum Mol Genet. 2018 Feb 15;27(4):757-758. doi: 10.1093/hmg/ddy025. Hum Mol Genet. 2018. PMID: 29351621 No abstract available.

10

Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.

Tian WT, Huang XJ, Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L. Tian WT, et al. Among authors: cao l. Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. Epub 2018 Jan 22. Mov Disord. 2018. PMID: 29356177

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