Cao L - Search Results

1

Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1-Related Hyperekplexia.

Zhan F, Zhang C, Wang S, Zhu Z, Chen G, Zhao M, Cao L. Zhan F, et al. Among authors: cao l. J Clin Neurol. 2020 Apr;16(2):230-236. doi: 10.3988/jcn.2020.16.2.230. J Clin Neurol. 2020. PMID: 32319239 Free PMC article.

2

Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients.

Huang XJ, Wang T, Wang JL, Liu XL, Che XQ, Li J, Mao X, Zhang M, Bi GH, Wu L, Zhang Y, Wang JY, Shen JY, Tang BS, Cao L, Chen SD. Huang XJ, et al. Among authors: cao l. Neurology. 2015 Nov 3;85(18):1546-53. doi: 10.1212/WNL.0000000000002079. Epub 2015 Oct 7. Neurology. 2015. PMID: 26446061

3

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.

4

The study of exercise tests in paroxysmal kinesigenic dyskinesia.

Zhou HY, Zhan FX, Tian WT, Zhang C, Wang Y, Zhu ZY, Liu XL, Xu YQ, Luan XH, Huang XJ, Chen SD, Cao L. Zhou HY, et al. Among authors: cao l. Clin Neurophysiol. 2018 Nov;129(11):2435-2441. doi: 10.1016/j.clinph.2018.09.004. Epub 2018 Sep 15. Clin Neurophysiol. 2018. PMID: 30293034 Clinical Trial.

5

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.

6

ATL3 gene mutation in a Chinese family with hereditary sensory neuropathy type 1F.

Xu H, Zhang C, Cao L, Song J, Xu X, Zhang B, Chen B, Zhao G. Xu H, et al. Among authors: cao l. J Peripher Nerv Syst. 2019 Mar;24(1):150-155. doi: 10.1111/jns.12309. Epub 2019 Feb 21. J Peripher Nerv Syst. 2019. PMID: 30680846

7

Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review.

Tian WT, Luan XH, Zhou HY, Zhang C, Huang XJ, Liu XL, Chen SD, Tang HD, Cao L. Tian WT, et al. Among authors: cao l. Neuromuscul Disord. 2019 Apr;29(4):282-289. doi: 10.1016/j.nmd.2019.01.001. Epub 2019 Jan 6. Neuromuscul Disord. 2019. PMID: 30737079 Review.

8

Teaching Video NeuroImages: Cautious walking gait in siblings with hereditary hyperekplexia.

Zhang C, Wang SG, Wang Y, Liu XL, Cao L. Zhang C, et al. Among authors: cao l. Neurology. 2019 Apr 23;92(17):e2068-e2069. doi: 10.1212/WNL.0000000000007375. Neurology. 2019. PMID: 31010918 No abstract available.

9

Lysosomal degradation of GMPPB is associated with limb-girdle muscular dystrophy type 2T.

Tian WT, Zhou HY, Zhan FX, Zhu ZY, Yang J, Chen SD, Luan XH, Cao L. Tian WT, et al. Among authors: cao l. Ann Clin Transl Neurol. 2019 May 8;6(6):1062-1071. doi: 10.1002/acn3.787. eCollection 2019 Jun. Ann Clin Transl Neurol. 2019. PMID: 31211170 Free PMC article.

10

Primary familial brain calcification presenting as paroxysmal kinesigenic dyskinesia: Genetic and functional analyses.

Zhan FX, Tian WT, Zhang C, Zhu ZY, Wang SG, Huang XJ, Cao L. Zhan FX, et al. Among authors: cao l. Neurosci Lett. 2020 Jan 1;714:134543. doi: 10.1016/j.neulet.2019.134543. Epub 2019 Oct 13. Neurosci Lett. 2020. PMID: 31618668

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