Li LX - Search Results

1

Genetic spectrum and clinical features in a cohort of Chinese patients with isolated dystonia.

Li LX, Liu Y, Huang JH, Yang Y, Pan YG, Zhang XL, Pan LZ, Jin LJ. Li LX, et al. Clin Genet. 2023 Apr;103(4):459-465. doi: 10.1111/cge.14298. Epub 2023 Jan 24. Clin Genet. 2023. PMID: 36648081

2

Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease.

Chen CX, Dong HL, Wei Q, Li LX, Yu H, Li JQ, Liu GL, Li HF, Bai G, Ma H, Wu ZY. Chen CX, et al. Among authors: li hf, li jq, li lx. Clin Genet. 2019 Nov;96(5):439-448. doi: 10.1111/cge.13616. Epub 2019 Aug 8. Clin Genet. 2019. PMID: 31372974

3

Synkinesis in primary and postparalytic hemifacial spasm: Clinical features and therapeutic outcomes of botulinum toxin A treatment.

Su JH, Yang MN, Teng F, Zhang XL, Pan YG, Hu Y, Xiao LB, Pan LZ, Li LX, Jin LJ. Su JH, et al. Among authors: li lx. Toxicon. 2020 Sep;184:122-126. doi: 10.1016/j.toxicon.2020.06.004. Epub 2020 Jun 14. Toxicon. 2020. PMID: 32553733

4

The expanding clinical and genetic spectrum of ANO3 dystonia.

Jiang LT, Li LX, Liu Y, Zhang XL, Pan YG, Wang L, Wan XH, Jin LJ. Jiang LT, et al. Among authors: li lx. Neurosci Lett. 2021 Feb 16;746:135590. doi: 10.1016/j.neulet.2020.135590. Epub 2020 Dec 31. Neurosci Lett. 2021. PMID: 33388357

5

Mutation screening of VPS16 gene in patients with isolated dystonia.

Li LX, Jiang LT, Liu Y, Zhang XL, Pan YG, Pan LZ, Nie ZY, Wan XH, Jin LJ. Li LX, et al. Parkinsonism Relat Disord. 2021 Feb;83:63-65. doi: 10.1016/j.parkreldis.2020.12.014. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33482438

6

Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoparesis.

Li LX, Jiang LT, Pan YG, Zhang XL, Pan LZ, Nie ZY, Chen YH, Jin LJ. Li LX, et al. J Mol Neurosci. 2021 Dec;71(12):2462-2467. doi: 10.1007/s12031-021-01831-9. Epub 2021 Apr 1. J Mol Neurosci. 2021. PMID: 33791913

7

The relationship between allergic diseases and tic disorders: A systematic review and meta-analysis.

Huang J, Li R, Li L, Song Y, Jin L. Huang J, et al. Neurosci Biobehav Rev. 2022 Jan;132:362-377. doi: 10.1016/j.neubiorev.2021.12.004. Epub 2021 Dec 6. Neurosci Biobehav Rev. 2022. PMID: 34883165 Review.

8

Whole-Exome Sequencing Identified Rare Variants in PCDHGB1 in Patients with Adult-Onset Dystonia.

Li LX, Huang JH, Pan LZ, Zhang XL, Pan YG, Jin LJ. Li LX, et al. Mov Disord. 2022 May;37(5):1099-1101. doi: 10.1002/mds.28965. Epub 2022 Mar 1. Mov Disord. 2022. PMID: 35229923 No abstract available.

9

Aberrant Neuregulin 1/ErbB Signaling in Charcot-Marie-Tooth Type 4D Disease.

Jiang LT, Chen YH, Huang JH, Tong WF, Jin LJ, Li LX. Jiang LT, et al. Among authors: li lx. Mol Cell Biol. 2022 Jul 21;42(7):e0055921. doi: 10.1128/mcb.00559-21. Epub 2022 Jun 16. Mol Cell Biol. 2022. PMID: 35708320 Free PMC article.

10

Transcriptional Profiling Reveals Brain Region-Specific Gene Networks Regulated in Exercise in a Mouse Model of Parkinson's Disease.

Tong W, Zhang K, Yao H, Li L, Hu Y, Zhang J, Song Y, Guan Q, Li S, Sun YE, Jin L. Tong W, et al. Front Aging Neurosci. 2022 Jun 23;14:891644. doi: 10.3389/fnagi.2022.891644. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35813950 Free PMC article.

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