Zhang L - Search Results

1

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: zhang l, zhang y. Seizure. 2019 Jul;69:228-234. doi: 10.1016/j.seizure.2019.05.010. Epub 2019 May 13. Seizure. 2019. PMID: 31112829 Free article.

2

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: zhang l, zhang j, zhang y. 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.

3

Clinical Analysis of Chronic Active Epstein-Barr Virus Infection Involving the Gastrointestinal Tract.

Wei A, Li Z, Ma H, Zhang L, Zhang J, He L, Lian H, Zhang Q, Chen S, Xu J, Wang D, Liu W, Zhang R, Wang T. Wei A, et al. Among authors: zhang l, zhang r, zhang q, zhang j. Pediatr Infect Dis J. 2023 Jan 1;42(1):13-19. doi: 10.1097/INF.0000000000003734. Epub 2022 Oct 11. Pediatr Infect Dis J. 2023. PMID: 36476520

4

The clinical characters and gene detection in a familial temporal lobe epilepsy with auditory aura.

Zhang L, Jia Y, Wang Y. Zhang L, et al. J Clin Neurosci. 2020 Apr;74:268-270. doi: 10.1016/j.jocn.2020.01.091. Epub 2020 Feb 5. J Clin Neurosci. 2020. PMID: 32035795

5

SCN1A-Related Epilepsy: Novel Mutations and Rare Phenotypes.

Ma R, Duan Y, Zhang L, Qi X, Zhang L, Pan S, Gao L, Wang C, Wang Y. Ma R, et al. Among authors: zhang l. Front Mol Neurosci. 2022 May 19;15:826183. doi: 10.3389/fnmol.2022.826183. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35663268 Free PMC article.

6

Quinidine Therapy for Lennox-Gastaut Syndrome With KCNT1 Mutation. A Case Report and Literature Review.

Jia Y, Lin Y, Li J, Li M, Zhang Y, Hou Y, Liu A, Zhang L, Li L, Xiang P, Ye J, Huang Z, Wang Y. Jia Y, et al. Among authors: zhang l, zhang y. Front Neurol. 2019 Feb 5;10:64. doi: 10.3389/fneur.2019.00064. eCollection 2019. Front Neurol. 2019. PMID: 30804880 Free PMC article.

7

Genetic characterization of pediatric primary hemophagocytic lymphohistiocytosis in China: a single-center study.

Zhang L, Li Z, Liu W, Ma H, Wang T, Zhang R. Zhang L, et al. Among authors: zhang r. Ann Hematol. 2019 Oct;98(10):2303-2310. doi: 10.1007/s00277-019-03764-1. Epub 2019 Aug 6. Ann Hematol. 2019. PMID: 31388699

8

[Clinical manifestation and EEG characteristics of Angelman syndrome].

Yang XY, Zou LP, Song F, Zhang LP, Zheng H, Wu HS, Xiao J. Yang XY, et al. Zhonghua Er Ke Za Zhi. 2010 Oct;48(10):783-6. Zhonghua Er Ke Za Zhi. 2010. PMID: 21176491 Chinese.

9

Trihexyphenidyl for treatment of dystonia in ataxia telangiectasia: a case report.

Zhang L, Jia Y, Qi X, Li M, Wang S, Wang Y. Zhang L, et al. Childs Nerv Syst. 2020 Apr;36(4):873-875. doi: 10.1007/s00381-019-04399-3. Epub 2019 Nov 5. Childs Nerv Syst. 2020. PMID: 31691010

10

Clinical Classifications of Children With Psychogenic Non-epileptic Seizure.

Zhang LP, Jia Y, Huang H, Li DW, Wang YP. Zhang LP, et al. Front Pediatr. 2021 Jan 25;8:596781. doi: 10.3389/fped.2020.596781. eCollection 2020. Front Pediatr. 2021. PMID: 33569360 Free PMC article.

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