Huang H - Search Results

1

Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families.

Wang Z, Song Y, Wang X, Li X, Xu F, Si L, Dong Y, Yao T, Zhu J, Lai H, Li W, Lin F, Huang H, Wang C. Wang Z, et al. Among authors: huang h. Neurosci Lett. 2021 May 1;752:135831. doi: 10.1016/j.neulet.2021.135831. Epub 2021 Mar 18. Neurosci Lett. 2021. PMID: 33746006 Free article.

2

The Antagonism of 5-HT6 Receptor Attenuates Current-Induced Spikes and Improves Long-Term Potentiation via the Regulation of M-Currents in a Pilocarpine-Induced Epilepsy Model.

Zhu C, Lin R, Liu C, Huang M, Lin F, Zhang G, Zhang Y, Miao J, Lin W, Huang H. Zhu C, et al. Among authors: huang m, huang h. Front Pharmacol. 2020 Apr 28;11:475. doi: 10.3389/fphar.2020.00475. eCollection 2020. Front Pharmacol. 2020. PMID: 32425770 Free PMC article.

3

Sequencing of neurofilament genes identified NEFH Ser787Arg as a novel risk variant of sporadic amyotrophic lateral sclerosis in Chinese subjects.

Lin F, Lin W, Zhu C, Lin J, Zhu J, Li XY, Wang Z, Wang C, Huang H. Lin F, et al. Among authors: huang h. BMC Med Genomics. 2021 Sep 11;14(1):222. doi: 10.1186/s12920-021-01073-z. BMC Med Genomics. 2021. PMID: 34511133 Free PMC article.

4

Predicting cognitive impairment in outpatients with epilepsy using machine learning techniques.

Lin F, Han J, Xue T, Lin J, Chen S, Zhu C, Lin H, Chen X, Lin W, Huang H. Lin F, et al. Among authors: huang h. Sci Rep. 2021 Oct 8;11(1):20002. doi: 10.1038/s41598-021-99506-3. Sci Rep. 2021. PMID: 34625614 Free PMC article.

5

Potential Pleiotropic Genes and Shared Biological Pathways in Epilepsy and Depression Based on GWAS Summary Statistics.

Lin H, Lin WH, Lin F, Liu CY, Che CH, Huang HP. Lin H, et al. Among authors: huang hp. Comput Intell Neurosci. 2022 Apr 12;2022:6799285. doi: 10.1155/2022/6799285. eCollection 2022. Comput Intell Neurosci. 2022. Retraction in: Comput Intell Neurosci. 2023 Dec 13;2023:9840787. doi: 10.1155/2023/9840787. PMID: 35463244 Free PMC article. Retracted.

6

[Analysis of CLCN1 gene mutations in 2 patients with myotonia congenita].

Chen ZT, He J, Chen WJ, Chen SG, Lin JL, Ye QY, Huang HP. Chen ZT, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):690-2. doi: 10.3760/cma.j.issn.1003-9406.2012.06.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225051 Chinese.

7

Seizure-induced 5-HT release and chronic impairment of serotonergic function in rats.

Lin WH, Huang HP, Lin MX, Chen SG, Lv XC, Che CH, Lin JL. Lin WH, et al. Neurosci Lett. 2013 Feb 8;534:1-6. doi: 10.1016/j.neulet.2012.12.007. Epub 2012 Dec 28. Neurosci Lett. 2013. PMID: 23276638

8

Mild clinical manifestation and unusual recovery upon coenzyme Q₁₀ treatment in the first Chinese Leigh syndrome pedigree with mutation m.10197 G>A.

Chen Z, Zhao Z, Ye Q, Chen Y, Pan X, Sun B, Huang H, Zheng A. Chen Z, et al. Among authors: huang h. Mol Med Rep. 2015 Mar;11(3):1956-62. doi: 10.3892/mmr.2014.2911. Epub 2014 Nov 10. Mol Med Rep. 2015. PMID: 25384404

9

Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.

Chen S, Zhou RL, Zhang W, Che CH, Feng SY, Huang HP, Liu CY, Zou ZY. Chen S, et al. Neurobiol Aging. 2021 Nov;107:168-173. doi: 10.1016/j.neurobiolaging.2021.05.017. Epub 2021 Jun 1. Neurobiol Aging. 2021. PMID: 34175147

10

Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients.

Feng SY, Lin H, Che CH, Huang HP, Liu CY, Zou ZY. Feng SY, et al. Among authors: huang hp. Front Neurol. 2022 Feb 7;13:790082. doi: 10.3389/fneur.2022.790082. eCollection 2022. Front Neurol. 2022. PMID: 35197922 Free PMC article.

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