Ji XN - Search Results

1

[A phenotypic and genetic study on β-propeller protein-associated neurodegeneration].

Li WH, Chen Q, Wang H, Zhang YF, Yang Y, Liu AJ, Liu WT, Ji XN, Teng ZT, Chen YC, Wu BB, Yang HW, Wang Y, Zhang YH, Zhou SZ. Li WH, et al. Among authors: ji xn. Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):830-836. doi: 10.3760/cma.j.issn.0578-1310.2019.11.004. Zhonghua Er Ke Za Zhi. 2019. PMID: 31665836 Chinese.

2

[Co-morbidity of attention deficit hyperactivity disorder in children with epilepsy].

Han Y, Qin J, Jiang YW, Chen J, Ji XN, Lin Q. Han Y, et al. Among authors: ji xn. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Feb;14(2):89-92. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22357462 Free article. Chinese.

3

[Glucose transporter 1 deficiency syndrome: features of movement disorders, diagnosis and treatment].

Ji XN, Xu CJ, Gao ZJ, Chen SH, Xu KM, Chen Q. Ji XN, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Mar;20(3):209-213. doi: 10.7499/j.issn.1008-8830.2018.03.009. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 29530121 Free PMC article. Chinese.

4

[Study of de novo point mutations in known genes among patients with unexplained intellectual disability or developmental delay].

Gao ZJ, Jiang Q, Chen XL, Chen Q, Ji XN, Mao YY, Feng S, Dong JJ, Xu KM. Gao ZJ, et al. Among authors: ji xn. Zhonghua Yi Xue Za Zhi. 2018 Nov 13;98(42):3426-3432. doi: 10.3760/cma.j.issn.0376-2491.2018.42.010. Zhonghua Yi Xue Za Zhi. 2018. PMID: 30440138 Chinese.

5

A Novel WDR45 Mutation in a 9-Month-Old Male Infant with Epileptic Spasms.

Liu WT, Chen Q, Gao ZJ, Ji XN, Xu KM, Cao YY. Liu WT, et al. Among authors: ji xn. Chin Med J (Engl). 2018 Dec 20;131(24):2991-2992. doi: 10.4103/0366-6999.247216. Chin Med J (Engl). 2018. PMID: 30539914 Free PMC article. No abstract available.

6

Status epilepticus associated with Mycoplasma pneumoniae encephalitis in children: good prognosis following early diagnosis and treatment.

Feng S, Chen JX, Zheng P, Zhang JZ, Gao ZJ, Mao YY, Ji XN, Chen SH, Sun HM, Chen Q. Feng S, et al. Among authors: ji xn. Chin Med J (Engl). 2019 Jun 20;132(12):1494-1496. doi: 10.1097/CM9.0000000000000233. Chin Med J (Engl). 2019. PMID: 31205112 Free PMC article. No abstract available.

7

Pediatric Autoimmune Encephalitis: Case Series From Two Chinese Tertiary Pediatric Neurology Centers.

Zhang J, Ji T, Chen Q, Jiang Y, Cheng H, Zheng P, Ma W, Lei T, Zhang Y, Jin Y, Wei C, Wu Y, Chang X, Bao X, Zhang Y, Xiong H, Ji X, Feng S, Ren H, Yang J, Jiang Y. Zhang J, et al. Front Neurol. 2019 Aug 22;10:906. doi: 10.3389/fneur.2019.00906. eCollection 2019. Front Neurol. 2019. PMID: 31507515 Free PMC article.

8

[Clinical and genetic characteristics of children with STXBP1 encephalopathy].

Cao JJ, Ji XN, Mao YY, Zhang PP, Liu WT, Zhang HZ, Ding N, Chen Q. Cao JJ, et al. Among authors: ji xn. Zhonghua Er Ke Za Zhi. 2020 Jun 2;58(6):493-498. doi: 10.3760/cma.j.cn112140-20191028-00683. Zhonghua Er Ke Za Zhi. 2020. PMID: 32521962 Chinese.

9

Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion.

Ji X, Gao Y, Zhang P, Jin Z, Zhang Y, Yang M, Zhang X, Chen Q. Ji X, et al. Stem Cell Res. 2022 Mar;59:102634. doi: 10.1016/j.scr.2021.102634. Epub 2022 Jan 3. Stem Cell Res. 2022. PMID: 34995844 Free article.

10

Drug-resistant epilepsy in children with hemophilia: how can we do it surgically?

Gong M, Li Y, Chen Q, Ma K, Tan B, Qin G, Yi L, Ji X, Mao Y. Gong M, et al. Br J Neurosurg. 2023 Oct;37(5):1124-1130. doi: 10.1080/02688697.2022.2039374. Epub 2022 Feb 17. Br J Neurosurg. 2023. PMID: 35174742

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