Xiong J - Search Results

1

[A family with Allan-Herndon-Dudley syndrome due to SLC16A2 gene mutation].

Tang YL, Peng J, Xiong J, Pang N, Wu LW, Yang HY, Kessi M, Yin F. Tang YL, et al. Among authors: xiong j. Zhonghua Er Ke Za Zhi. 2018 Nov 2;56(11):829-834. doi: 10.3760/cma.j.issn.0578-1310.2018.11.008. Zhonghua Er Ke Za Zhi. 2018. PMID: 30392207 Chinese.

2

[Recurrent convulsion and pulmonary infection complicated by psychomotor retardation in an infant].

Xiong J, Peng J, Duan HL, Chen C, Wang XL, Chen SM, Yin F. Xiong J, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2018 Feb;20(2):154-157. doi: 10.7499/j.issn.1008-8830.2018.02.014. Zhongguo Dang Dai Er Ke Za Zhi. 2018. PMID: 29429466 Free PMC article. Chinese.

3

Next-generation sequencing improves treatment efficacy and reduces hospitalization in children with drug-resistant epilepsy.

Peng J, Pang N, Wang Y, Wang XL, Chen J, Xiong J, Peng P, Zhu CH, Kessi MB, He F, Yin F. Peng J, et al. Among authors: xiong j. CNS Neurosci Ther. 2019 Jan;25(1):14-20. doi: 10.1111/cns.12869. Epub 2018 Jun 22. CNS Neurosci Ther. 2019. PMID: 29933521 Free PMC article.

4

Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review.

Kessi M, Peng J, Yang L, Xiong J, Duan H, Pang N, Yin F. Kessi M, et al. Among authors: xiong j. BMC Genet. 2018 Jul 6;19(1):40. doi: 10.1186/s12863-018-0628-5. BMC Genet. 2018. PMID: 29976148 Free PMC article.

5

Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.

Kessi M, Xiong J, Wu L, Yang L, He F, Chen C, Pang N, Duan H, Zhang W, Arafat A, Yin F, Peng J. Kessi M, et al. Among authors: xiong j. Front Neurol. 2018 Nov 19;9:947. doi: 10.3389/fneur.2018.00947. eCollection 2018. Front Neurol. 2018. PMID: 30510536 Free PMC article.

6

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes.

Xiong J, Chen S, Pang N, Deng X, Yang L, He F, Wu L, Chen C, Yin F, Peng J. Xiong J, et al. Front Neurosci. 2019 Apr 11;13:349. doi: 10.3389/fnins.2019.00349. eCollection 2019. Front Neurosci. 2019. PMID: 31031587 Free PMC article.

7

[A case of Okur-Chung syndrome caused by CSNK2A1 gene variation and review of literature].

Duan HL, Peng J, Pang N, Chen SM, Xiong J, Guang SQ, Yin F. Duan HL, et al. Among authors: xiong j. Zhonghua Er Ke Za Zhi. 2019 May 2;57(5):368-372. doi: 10.3760/cma.j.issn.0578-1310.2019.05.010. Zhonghua Er Ke Za Zhi. 2019. PMID: 31060130 Review. Chinese.

8

[Application of ventricular shunt for children with post-infective hydrocephalus].

Chen S, Peng J, Deng X, Wu L, Xiong J, Duan H, Peng P, Yin F. Chen S, et al. Among authors: xiong j. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2019 Nov 28;44(11):1230-1237. doi: 10.11817/j.issn.1672-7347.2019.180345. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2019. PMID: 31919317 Free article. Chinese.

9

The Recommendations for the Management of Chinese Children With Epilepsy During the COVID-19 Outbreak.

Chen B, Kessi M, Chen S, Xiong J, Wu L, Deng X, Yang L, He F, Yin F, Peng J. Chen B, et al. Among authors: xiong j. Front Pediatr. 2020 Aug 25;8:495. doi: 10.3389/fped.2020.00495. eCollection 2020. Front Pediatr. 2020. PMID: 32984209 Free PMC article.

10

De novo variants of DEAF1 cause intellectual disability in six Chinese patients.

Chen S, Deng X, Xiong J, He F, Yang L, Chen B, Chen C, Zhang C, Yang L, Peng J, Yin F. Chen S, et al. Among authors: xiong j. Clin Chim Acta. 2021 Jul;518:17-21. doi: 10.1016/j.cca.2021.02.026. Epub 2021 Mar 9. Clin Chim Acta. 2021. PMID: 33705764

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