Shi YW - Search Results

1

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

Xu XX, Liu XR, Fan CY, Lai JX, Shi YW, Yang W, Su T, Xu JY, Luo JH, Liao WP. Xu XX, et al. Among authors: shi yw. Neurosci Bull. 2018 Apr;34(2):237-246. doi: 10.1007/s12264-017-0182-6. Epub 2017 Sep 21. Neurosci Bull. 2018. PMID: 28936771 Free PMC article.

2

Identification of the promoter region and the 5'-untranslated exons of the human voltage-gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5'-untranslated exons.

Long YS, Zhao QH, Su T, Cai YL, Zeng Y, Shi YW, Yi YH, Chang HH, Liao WP. Long YS, et al. Among authors: shi yw. J Neurosci Res. 2008 Nov 15;86(15):3375-81. doi: 10.1002/jnr.21790. J Neurosci Res. 2008. PMID: 18655196

3

[Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome].

Song XW, Wang YL, Shi YW, Deng WY, Chen SQ, Lin H, Yi YH, Liao WP. Song XW, et al. Among authors: shi yw. Zhonghua Yi Xue Za Zhi. 2009 Dec 22;89(47):3320-3. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20193558 Chinese.

4

Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: associated with loss of function of Na(v) 1.1.

Liao WP, Shi YW, Long YS, Zeng Y, Li T, Yu MJ, Su T, Deng P, Lei ZG, Xu SJ, Deng WY, Liu XR, Sun WW, Yi YH, Xu ZC, Duan S. Liao WP, et al. Among authors: shi yw. Epilepsia. 2010 Sep;51(9):1669-78. doi: 10.1111/j.1528-1167.2010.02645.x. Epub 2010 Jun 7. Epilepsia. 2010. PMID: 20550552 Free article.

5

Milder phenotype with SCN1A truncation mutation other than SMEI.

Yu MJ, Shi YW, Gao MM, Deng WY, Liu XR, Chen L, Long YS, Yi YH, Liao WP. Yu MJ, et al. Among authors: shi yw. Seizure. 2010 Sep;19(7):443-5. doi: 10.1016/j.seizure.2010.06.010. Epub 2010 Jul 14. Seizure. 2010. PMID: 20630778 Free article.

6

[Hypersensitivity syndrome reactions to antiepileptic drugs, clinical characteristic and association with HLA-B*1502].

Sun D, Shi YW, Liu ZS, Liao WP, Wang FL, Wu GF, Hu JS, He CY. Sun D, et al. Among authors: shi yw. Zhonghua Yi Xue Za Zhi. 2010 Oct 26;90(39):2763-6. Zhonghua Yi Xue Za Zhi. 2010. PMID: 21162913 Chinese.

7

HLA-B*1502 genotyping in two Chinese patients with phenytoin-induced Stevens-Johnson syndrome.

Min FL, Shi YW, Liu XR, Liao WP. Min FL, et al. Among authors: shi yw. Epilepsy Behav. 2011 Feb;20(2):390-1. doi: 10.1016/j.yebeh.2010.11.022. Epub 2011 Jan 7. Epilepsy Behav. 2011. PMID: 21216202

8

Promoter analysis of mouse Scn3a gene and regulation of the promoter activity by GC box and CpG methylation.

Deng GF, Qin JM, Sun XS, Kuang ZY, Su T, Zhao QH, Shi YW, Liu XR, Yu MJ, Yi YH, Liao WP, Long YS. Deng GF, et al. Among authors: shi yw. J Mol Neurosci. 2011 Jun;44(2):115-21. doi: 10.1007/s12031-011-9492-8. Epub 2011 Jan 27. J Mol Neurosci. 2011. PMID: 21271300

9

Hla-B alleles and lamotrigine-induced cutaneous adverse drug reactions in the Han Chinese population.

Shi YW, Min FL, Liu XR, Zan LX, Gao MM, Yu MJ, Liao WP. Shi YW, et al. Basic Clin Pharmacol Toxicol. 2011 Jul;109(1):42-6. doi: 10.1111/j.1742-7843.2011.00681.x. Epub 2011 Mar 16. Basic Clin Pharmacol Toxicol. 2011. PMID: 21306565 Free article.

10

HLA-B*1502 screening and toxic effects of carbamazepine.

Liao WP, Shi YW, Min FL. Liao WP, et al. Among authors: shi yw. N Engl J Med. 2011 Aug 18;365(7):672-3; author reply 673. doi: 10.1056/NEJMc1105467. N Engl J Med. 2011. PMID: 21848471 No abstract available.

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