Tang JG - Search Results

1

Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain.

Xie XH, Tang JG, Liu ZH, Peng SJ, Yuan ZZ, Gu H, Hu YQ, Tan ZP. Xie XH, et al. Among authors: tang jg. Front Neurosci. 2021 Jul 14;15:697167. doi: 10.3389/fnins.2021.697167. eCollection 2021. Front Neurosci. 2021. PMID: 34335171 Free PMC article.

2

Synthesis and analgesic effects of μ-TRTX-Hhn1b on models of inflammatory and neuropathic pain.

Liu Y, Tang J, Zhang Y, Xun X, Tang D, Peng D, Yi J, Liu Z, Shi X. Liu Y, et al. Toxins (Basel). 2014 Aug 13;6(8):2363-78. doi: 10.3390/toxins6082363. Toxins (Basel). 2014. PMID: 25123556 Free PMC article.

3

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Zeng H, Tang JG, Yang YF, Tan ZP, Tan JQ. Zeng H, et al. Among authors: tang jg. Cytogenet Genome Res. 2017;152(1):16-21. doi: 10.1159/000477428. Epub 2017 Jun 29. Cytogenet Genome Res. 2017. PMID: 28658676

4

Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis.

Huang H, Wang Y, Cao Y, Wu B, Li Y, Fan L, Tan Z, Jiang Y, Tang J, Hu J, Shi X. Huang H, et al. Sci Rep. 2017 Aug 29;7(1):9686. doi: 10.1038/s41598-017-09671-7. Sci Rep. 2017. PMID: 28851954 Free PMC article.

5

Case report: Desquamating dermatitis, bilateral cerebellar lesions in a late-onset methylmalonic acidemia patient.

Chen Q, Tang J, Zhang H, Qin L. Chen Q, et al. Front Neurol. 2023 Sep 22;14:1255128. doi: 10.3389/fneur.2023.1255128. eCollection 2023. Front Neurol. 2023. PMID: 37808496 Free PMC article.

6

Case report: Episodic psychosis caused by a novel SCP2 splicing mutation.

Tang H, Luo Y, Tang Z, Tang J, Fang J. Tang H, et al. Front Neurol. 2023 Oct 12;14:1270793. doi: 10.3389/fneur.2023.1270793. eCollection 2023. Front Neurol. 2023. PMID: 37905191 Free PMC article.

7

A Novel SCN9A Mutation (F826Y) in Primary Erythromelalgia Alters the Excitability of Nav1.7.

Wu B, Zhang Y, Tang H, Yang M, Long H, Shi G, Tang J, Shi X. Wu B, et al. Curr Mol Med. 2017;17(6):450-457. doi: 10.2174/1566524017666171009105029. Curr Mol Med. 2017. PMID: 28990532

8

Preservation of neuronal functions by exosomes derived from different human neural cell types under ischemic conditions.

Deng M, Xiao H, Peng H, Yuan H, Xu Y, Zhang G, Tang J, Hu Z. Deng M, et al. Eur J Neurosci. 2018 Jan;47(2):150-157. doi: 10.1111/ejn.13784. Epub 2017 Dec 15. Eur J Neurosci. 2018. PMID: 29178548

9

Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series.

Tang Z, Gao S, He M, Chen Q, Fang J, Luo Y, Yan W, Shi X, Huang H, Tang J. Tang Z, et al. Front Neurol. 2021 Nov 8;12:747360. doi: 10.3389/fneur.2021.747360. eCollection 2021. Front Neurol. 2021. PMID: 34819910 Free PMC article.

10

Case Report: Diagnosis of Acute Q Fever With Aseptic Meningitis in a Patient by Using Metagenomic Next-Generation Sequencing.

Gu M, Mo X, Tang Z, Tang J, Wang W. Gu M, et al. Front Med (Lausanne). 2022 May 18;9:855020. doi: 10.3389/fmed.2022.855020. eCollection 2022. Front Med (Lausanne). 2022. PMID: 35665349 Free PMC article.

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