Zeng Q - Search Results

1

ATP1A3 mosaicism in families with alternating hemiplegia of childhood.

Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. Yang X, et al. Among authors: zeng q. Clin Genet. 2019 Jul;96(1):43-52. doi: 10.1111/cge.13539. Epub 2019 Apr 3. Clin Genet. 2019. PMID: 30891744 Free PMC article.

2

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort.

Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. Yang X, et al. Among authors: zeng q. Sci Rep. 2017 Nov 15;7(1):15677. doi: 10.1038/s41598-017-15814-7. Sci Rep. 2017. PMID: 29142202 Free PMC article.

3

[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome].

Zeng Q, Zhang Y, Yang X, Xu X, Zhang J, Tian X, Liu A, Liu X, Jiang Y, Wu X. Zeng Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):787-791. doi: 10.3760/cma.j.issn.1003-9406.2017.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188601 Chinese.

4

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

Zeng Q, Yang X, Zhang J, Liu A, Yang Z, Liu X, Wu Y, Wu X, Wei L, Zhang Y. Zeng Q, et al. J Hum Genet. 2018 Jan;63(1):9-18. doi: 10.1038/s10038-017-0359-x. Epub 2017 Nov 13. J Hum Genet. 2018. PMID: 29215089 Free PMC article. Clinical Trial.

5

The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome.

Tian X, Ye J, Zeng Q, Zhang J, Yang X, Liu A, Yang Z, Liu X, Wu X, Zhang Y. Tian X, et al. Among authors: zeng q. Dev Med Child Neurol. 2018 Jun;60(6):566-573. doi: 10.1111/dmcn.13727. Epub 2018 Mar 24. Dev Med Child Neurol. 2018. PMID: 29573403 Free article.

6

Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations.

Zhang J, Chen J, Zeng Q, Zhang L, Tian X, Yang X, Yang Z, Wu Y, Wu X, Zhang Y. Zhang J, et al. Among authors: zeng q. Seizure. 2019 Jul;69:228-234. doi: 10.1016/j.seizure.2019.05.010. Epub 2019 May 13. Seizure. 2019. PMID: 31112829 Free article.

7

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.

Burgess R, Wang S, McTague A, Boysen KE, Yang X, Zeng Q, Myers KA, Rochtus A, Trivisano M, Gill D; EIMFS Consortium; Sadleir LG, Specchio N, Guerrini R, Marini C, Zhang YH, Mefford HC, Kurian MA, Poduri AH, Scheffer IE. Burgess R, et al. Among authors: zeng q. Ann Neurol. 2019 Dec;86(6):821-831. doi: 10.1002/ana.25619. Ann Neurol. 2019. PMID: 31618474 Free PMC article.

8

CHD2-related epilepsy: novel mutations and new phenotypes.

Chen J, Zhang J, Liu A, Zhang L, Li H, Zeng Q, Yang Z, Yang X, Wu X, Zhang Y. Chen J, et al. Among authors: zeng q. Dev Med Child Neurol. 2020 May;62(5):647-653. doi: 10.1111/dmcn.14367. Epub 2019 Nov 1. Dev Med Child Neurol. 2020. PMID: 31677157 Free article.

9

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.

Yang Y, Zeng Q, Cheng M, Niu X, Xiangwei W, Gong P, Li W, Ma J, Zhang X, Yang X, Yang Z, Sun D, Zhou S, Liao J, Jiang Y, Zhang Y. Yang Y, et al. Among authors: zeng q. J Neurol. 2022 May;269(5):2649-2665. doi: 10.1007/s00415-021-10834-w. Epub 2021 Oct 26. J Neurol. 2022. PMID: 34698933

10

Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants.

Yang Y, Niu X, Cheng M, Zeng Q, Deng J, Tian X, Wang Y, Yu J, Shi W, Wu W, Ma J, Li Y, Yang X, Zhang X, Jia T, Yang Z, Liao J, Sun Y, Zheng H, Sun S, Sun D, Jiang Y, Zhang Y. Yang Y, et al. Among authors: zeng q. Front Mol Neurosci. 2022 Mar 14;15:809163. doi: 10.3389/fnmol.2022.809163. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35359574 Free PMC article.

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