He N - Search Results

1

DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders.

Wu WC, Liang XY, Zhang DM, Jin L, Liu ZG, Zeng XL, Zhai QX, Liao WP, He N, Meng XH. Wu WC, et al. Among authors: he n. Seizure. 2024 Mar;116:119-125. doi: 10.1016/j.seizure.2023.10.010. Epub 2023 Oct 27. Seizure. 2024. PMID: 37903666 Free article.

2

Cutaneous reactions induced by oxcarbazepine in Southern Han Chinese: incidence, features, risk factors and relation to HLA-B alleles.

He N, Min FL, Shi YW, Guo J, Liu XR, Li BM, Zhou JH, Ou YM, Liao JX, Liao WP. He N, et al. Seizure. 2012 Oct;21(8):614-8. doi: 10.1016/j.seizure.2012.06.014. Epub 2012 Jul 20. Seizure. 2012. PMID: 22818943 Free article.

3

The association between oxcarbazepine-induced maculopapular eruption and HLA-B alleles in a northern Han Chinese population.

Lv YD, Min FL, Liao WP, He N, Zeng T, Ma DH, Shi YW. Lv YD, et al. Among authors: he n. BMC Neurol. 2013 Jul 8;13:75. doi: 10.1186/1471-2377-13-75. BMC Neurol. 2013. PMID: 23829937 Free PMC article.

4

The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype.

Meng H, Xu HQ, Yu L, Lin GW, He N, Su T, Shi YW, Li B, Wang J, Liu XR, Tang B, Long YS, Yi YH, Liao WP. Meng H, et al. Among authors: he n. Hum Mutat. 2015 Jun;36(6):573-80. doi: 10.1002/humu.22782. Epub 2015 Apr 13. Hum Mutat. 2015. PMID: 25754450

5

A Point Mutation in SCN1A 5' Genomic Region Decreases the Promoter Activity and Is Associated with Mild Epilepsy and Seizure Aggravation Induced by Antiepileptic Drug.

Gao QW, Hua LD, Wang J, Fan CX, Deng WY, Li B, Bian WJ, Shao CX, He N, Zhou P, Liao WP, Shi YW. Gao QW, et al. Among authors: he n. Mol Neurobiol. 2017 May;54(4):2428-2434. doi: 10.1007/s12035-016-9800-y. Epub 2016 Mar 11. Mol Neurobiol. 2017. PMID: 26969601

6

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene.

Liu XR, Huang D, Wang J, Wang YF, Sun H, Tang B, Li W, Lai JX, He N, Wu M, Su T, Meng H, Shi YW, Li BM, Tang BS, Liao WP. Liu XR, et al. Among authors: he n. Neurol Genet. 2016 Mar 22;2(2):e66. doi: 10.1212/NXG.0000000000000066. eCollection 2016 Apr. Neurol Genet. 2016. PMID: 27123484 Free PMC article.

7

Epilepsy-associated genes.

Wang J, Lin ZJ, Liu L, Xu HQ, Shi YW, Yi YH, He N, Liao WP. Wang J, et al. Among authors: he n. Seizure. 2017 Jan;44:11-20. doi: 10.1016/j.seizure.2016.11.030. Epub 2016 Dec 6. Seizure. 2017. PMID: 28007376 Free article. Review.

8

Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.

Wei F, Yan LM, Su T, He N, Lin ZJ, Wang J, Shi YW, Yi YH, Liao WP. Wei F, et al. Among authors: he n. Neurosci Bull. 2017 Aug;33(4):455-477. doi: 10.1007/s12264-017-0134-1. Epub 2017 May 9. Neurosci Bull. 2017. PMID: 28488083 Free PMC article. Review.

9

ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.

Wang JY, Zhou P, Wang J, Tang B, Su T, Liu XR, Li BM, Meng H, Shi YW, Yi YH, He N, Liao WP. Wang JY, et al. Among authors: he n. Neurogenetics. 2018 Jan;19(1):9-16. doi: 10.1007/s10048-017-0528-2. Epub 2017 Nov 13. Neurogenetics. 2018. PMID: 29130122

10

Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome.

He N, Li BM, Li ZX, Wang J, Liu XR, Meng H, Tang B, Bian WJ, Shi YW, Liao WP. He N, et al. J Neurodev Disord. 2018 Mar 20;10(1):10. doi: 10.1186/s11689-018-9229-x. J Neurodev Disord. 2018. PMID: 29558884 Free PMC article.

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