Li G - Search Results

1

Novel compound heterozygous mutations in the PARK2 gene identified in a Chinese pedigree with early-onset Parkinson's disease.

Shi Y, Kawakami H, Zang W, Li G, Zhang J, Xu C. Shi Y, et al. Among authors: li g. Brain Behav. 2017 Dec 19;8(1):e00901. doi: 10.1002/brb3.901. eCollection 2018 Jan. Brain Behav. 2017. PMID: 29568695 Free PMC article.

2

Magnetic resonance study on the brain structure and resting-state brain functional connectivity in primary insomnia patients.

Li G, Zhang X, Zhang J, Wang E, Zhang H, Li Y. Li G, et al. Among authors: li y. Medicine (Baltimore). 2018 Aug;97(34):e11944. doi: 10.1097/MD.0000000000011944. Medicine (Baltimore). 2018. PMID: 30142814 Free PMC article.

3

Circular RNA circ_0034642 elevates BATF3 expression and promotes cell proliferation and invasion through miR-1205 in glioma.

Yang M, Li G, Fan L, Zhang G, Xu J, Zhang J. Yang M, et al. Among authors: li g. Biochem Biophys Res Commun. 2019 Jan 15;508(3):980-985. doi: 10.1016/j.bbrc.2018.12.052. Epub 2018 Dec 11. Biochem Biophys Res Commun. 2019. PMID: 30551880

4

Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNAAsn gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome.

Fu J, Ma MM, Pang M, Yang L, Li G, Song J, Zhang JW. Fu J, et al. Among authors: li g. Chin Med J (Engl). 2019 Apr 5;132(7):865-867. doi: 10.1097/CM9.0000000000000151. Chin Med J (Engl). 2019. PMID: 30897601 Free PMC article. No abstract available.

5

Novel mutations in DPM3 cause dystroglycanopathy with central nervous system involvement.

Fu J, Ma M, Song J, Pang M, Yang L, Li G, Zhang J. Fu J, et al. Among authors: li g. Clin Genet. 2019 Dec;96(6):590-591. doi: 10.1111/cge.13634. Epub 2019 Aug 30. Clin Genet. 2019. PMID: 31469168 No abstract available.

6

[Analysis of a pedigree with autosomal dominant intermediate Charcot-Marie-Tooth disease type E and nephropathy].

Fu J, Ma M, Pang M, Yang L, Li G, Song J, Zhang J. Fu J, et al. Among authors: li g. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):918-921. doi: 10.3760/cma.j.issn.1003-9406.2019.09.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515790 Chinese.

7

BAG3 p.Pro209Ser mutation identified in a Chinese family with Charcot-Marie-Tooth disease.

Fu J, Ma M, Song J, Pang M, Li G, Zhang J. Fu J, et al. Among authors: li g. J Neurol. 2020 Apr;267(4):1080-1085. doi: 10.1007/s00415-019-09680-8. Epub 2019 Dec 18. J Neurol. 2020. PMID: 31853710

8

Lower limb muscle magnetic resonance imaging in Chinese patients with myotonic dystrophy type 1.

Song J, Fu J, Ma M, Pang M, Li G, Gao L, Zhang J. Song J, et al. Among authors: li g. Neurol Res. 2020 Feb;42(2):170-177. doi: 10.1080/01616412.2020.1716494. Epub 2020 Jan 17. Neurol Res. 2020. PMID: 31951783

9

Clinical and Genetic Features of Chinese Patients With NIPA1-Related Hereditary Spastic Paraplegia Type 6.

Fu J, Ma M, Li G, Zhang J. Fu J, et al. Among authors: li g. Front Genet. 2022 Apr 8;13:859688. doi: 10.3389/fgene.2022.859688. eCollection 2022. Front Genet. 2022. PMID: 35464835 Free PMC article.

10

[Analysis of a pedigree with distal hereditary motor neuropathy type 2A caused by mutation in HSPB8 gene].

Li G, Fu J, Pang M, Song J, Ma M, Zhang J. Li G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jun 10;39(6):621-624. doi: 10.3760/cma.j.cn511374-20210528-00450. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35773767 Chinese.

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