Zhuo XW - Search Results

1

[Analysis of clinical and genetic characteristics of epilepsy associated with chromosome 16p11.2 microdeletion].

Wang HS, Deng J, Wang XH, Chen CH, Wang X, Zhuo XW, Dai LF, Li H, Fang F. Wang HS, et al. Among authors: zhuo xw. Zhonghua Er Ke Za Zhi. 2022 Apr 2;60(4):339-344. doi: 10.3760/cma.j.cn112140-20211115-00953. Zhonghua Er Ke Za Zhi. 2022. PMID: 35385941 Chinese.

2

[Reversible ceftriaxone-associated biliary pseudolithiasis in three children with renal diseases].

Zhong XH, Chen H, Yao Y, Zhuo XW, Huang JP, Xiao HJ, Ai Y. Zhong XH, et al. Among authors: zhuo xw. Zhonghua Er Ke Za Zhi. 2010 Mar;48(3):216-9. Zhonghua Er Ke Za Zhi. 2010. PMID: 20426960 Chinese.

3

[Clinical and laboratory characteristics and genetic diagnosis of Kabuki syndrome].

Wang HM, Wang XH, Wu HS, Wu Y, Zhuo XW. Wang HM, et al. Among authors: zhuo xw. Zhonghua Er Ke Za Zhi. 2018 Nov 2;56(11):846-849. doi: 10.3760/cma.j.issn.0578-1310.2018.11.010. Zhonghua Er Ke Za Zhi. 2018. PMID: 30392209 Chinese.

4

[Clinical features of 19 children with Bickerstaff brainstem encephalitis].

Zhuo XW, Ding CH, Li JW, Zhang WH, Yang XY, Deng J, Tian XJ, Han TL, Fang F. Zhuo XW, et al. Zhonghua Er Ke Za Zhi. 2019 May 2;57(5):363-367. doi: 10.3760/cma.j.issn.0578-1310.2019.05.009. Zhonghua Er Ke Za Zhi. 2019. PMID: 31060129 Chinese.

5

[Mild Canavan disease in a child].

Zhou J, Ding CH, Zhuo XW, Ren XT, Zhang WH, Gong S. Zhou J, et al. Among authors: zhuo xw. Zhonghua Er Ke Za Zhi. 2019 Dec 2;57(12):961-963. doi: 10.3760/cma.j.issn.0578-1310.2019.12.014. Zhonghua Er Ke Za Zhi. 2019. PMID: 31795566 Chinese.

6

Neurologic Manifestations as Initial Clinical Presentation of Familial Hemophagocytic Lymphohistiocytosis Type2 Due to PRF1 Mutation in Chinese Pediatric Patients.

Feng WX, Yang XY, Li JW, Gong S, Wu Y, Zhang WH, Han TL, Zhuo XW, Ding CH, Fang F. Feng WX, et al. Among authors: zhuo xw. Front Genet. 2020 Mar 4;11:126. doi: 10.3389/fgene.2020.00126. eCollection 2020. Front Genet. 2020. PMID: 32194620 Free PMC article.

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: zhuo xw. 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: zhuo xw. 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

[Clinical and genetic analysis of 5 pediatric patients with hemiplegic migraine presenting as acute encephalopathy].

Zhuo XW, Ren SS, Gong S, Zhang WH, Li JW, Zhang YJ, Ding CH. Zhuo XW, et al. Zhonghua Er Ke Za Zhi. 2021 Apr 2;59(4):316-321. doi: 10.3760/cma.j.cn112140-20201015-00946. Zhonghua Er Ke Za Zhi. 2021. PMID: 33775052 Chinese.

10

[The etiology of 340 infants with early-onset epilepsy].

Song TY, Deng J, Fang F, Chen CH, Wang XH, Wang X, Zhuo XW, Dai LF, Wang HM, Tian XJ. Song TY, et al. Among authors: zhuo xw. Zhonghua Er Ke Za Zhi. 2021 May 2;59(5):387-392. doi: 10.3760/cma.j.cn112140-20201016-00947. Zhonghua Er Ke Za Zhi. 2021. PMID: 33902223 Chinese.

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