Ren XT - Search Results

1

[Phenotype and genotype of twelve Chinese children with mitochondrial DNA depletion syndromes].

Dai LF, Fang F, Liu ZM, Shen DM, Ding CH, Li JW, Ren XT, Wu HS. Dai LF, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2019 Mar 2;57(3):211-216. doi: 10.3760/cma.j.issn.0578-1310.2019.03.011. Zhonghua Er Ke Za Zhi. 2019. PMID: 30818899 Chinese.

2

[Clinical features and diagnosis of childhood leukoencephalopathy with cerebral calcifications and cysts in four cases].

Jin H, Wu HS, Ding CH, Jin Z, Huang Y, Zhou CJ, Zhang WH, Lyu JL, Dai LF, Ren XT, Ge M, Fang F. Jin H, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2018 Jul 2;56(7):539-544. doi: 10.3760/cma.j.issn.0578-1310.2018.07.013. Zhonghua Er Ke Za Zhi. 2018. PMID: 29996189 Chinese.

3

[Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation].

Chen CH, Wu HS, Wang XH, Wang HM, Zhang S, Lyu JL, Ren XT, Fang F, Chen GH. Chen CH, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2018 Nov 2;56(11):818-823. doi: 10.3760/cma.j.issn.0578-1310.2018.11.005. Zhonghua Er Ke Za Zhi. 2018. PMID: 30392205 Chinese.

4

[Phenotypic and genotypic characteristics of fever-induced paroxysmal weakness and encephalopathy caused by ATP1A3 pathogenic variants].

Zhang WH, Ren XT, Feng WX, Chen CH, Ding CH, Lyu JL, Han TL. Zhang WH, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2019 Jul 2;57(7):543-547. doi: 10.3760/cma.j.issn.0578-1310.2019.07.010. Zhonghua Er Ke Za Zhi. 2019. PMID: 31269555 Chinese.

5

[KMT2B variants responsible for children dystonia 28: report of two cases].

Dai LF, Ding CH, Fang T, Xie ZH, Liu TH, Zhang WH, Wang XH, Ren XT, Liu M, Tian XJ, Wu HS, Fang F. Dai LF, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2019 Jul 2;57(7):564-566. doi: 10.3760/cma.j.issn.0578-1310.2019.07.015. Zhonghua Er Ke Za Zhi. 2019. PMID: 31269560 Chinese.

6

[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].

Han XD, Fang F, Li H, Liu ZM, Shi YQ, Wang JL, Ren XT, Ding CH, Chen CH, Li JW, Zhang WH, Deng J. Han XD, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):844-851. doi: 10.3760/cma.j.issn.0578-1310.2019.11.006. Zhonghua Er Ke Za Zhi. 2019. PMID: 31665838 Chinese.

7

[Clinical observation on the overlapping syndrome of myelin oligodendrocyte glycoprotein antibody and anti-N-methyl-D aspartate receptor in children].

Gong S, Zhang WH, Ren HT, Li JW, Zhou J, Cheng H, Zhuo XW, Ren CH, Han TL, Lyu JL, Ding CH, Fang F, Guan HZ, Ren XT. Gong S, et al. Among authors: ren ch, ren ht, ren xt. Zhonghua Er Ke Za Zhi. 2020 Jul 2;58(7):581-585. doi: 10.3760/cma.j.cn112140-20191209-00788. Zhonghua Er Ke Za Zhi. 2020. PMID: 32605343 Chinese.

8

[Clinical features of anti-myelin oligodendrocyte glycoprotein antibody-associated diseases in children with cortical encephalitis].

Zhou J, Ding CH, Zhang WH, Zhuo XW, Li JW, Gong S, Guan HZ, Fang F, Zhu XY, Cheng H, Ren XT. Zhou J, et al. Among authors: ren xt. Zhonghua Yi Xue Za Zhi. 2020 Jul 7;100(25):1952-1955. doi: 10.3760/cma.j.cn112137-20200525-01644. Zhonghua Yi Xue Za Zhi. 2020. PMID: 32629595 Chinese.

9

[Pediatric autoimmune encephalitis associated with anti-glutamic acid decarboxylase 65 antibody: two cases report and literature review].

Ren CH, Ren HT, Ren XT, Zhang WH, Li JW, Dai LF, Chen CH, Guan HZ, Fang F. Ren CH, et al. Among authors: ren ht, ren xt. Zhonghua Er Ke Za Zhi. 2021 Jan 2;59(1):47-52. doi: 10.3760/cma.j.cn112140-20200705-00691. Zhonghua Er Ke Za Zhi. 2021. PMID: 33397004 Review. Chinese.

10

[Clinical characteristics and gene analysis of SYNGAP1-related epilepsy in children].

Tian XJ, Fang F, Ding CH, Ren XT, Wang X, Wang XF, Lyu JL, Jin H, Han TL, Deng J. Tian XJ, et al. Among authors: ren xt. Zhonghua Er Ke Za Zhi. 2021 Dec 2;59(12):1059-1064. doi: 10.3760/cma.j.cn112140-20210430-00369. Zhonghua Er Ke Za Zhi. 2021. PMID: 34856666 Chinese.

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