Peng 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: peng 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

[ORAI1 variation induced combined immunodeficiency: a case report and literature review].

Yang HY, Deng XL, Yin F, Peng J, Wu LW. Yang HY, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2019 Feb 2;57(2):142-145. doi: 10.3760/cma.j.issn.0578-1310.2019.02.015. Zhonghua Er Ke Za Zhi. 2019. PMID: 30695890 Review. Chinese.

3

[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: peng 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.

4

[Clinical analysis of 71 cases of anti-N-methyl-D-aspartate receptor encephalitis in children].

Wang GL, Yin F, Wang Y, Zhang WX, He F, Yang LF, Wu LW, Peng J. Wang GL, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2019 Feb 2;57(2):125-130. doi: 10.3760/cma.j.issn.0578-1310.2019.02.012. Zhonghua Er Ke Za Zhi. 2019. PMID: 30695887 Chinese.

5

[Dynamin-1-related infantile spasms: a case report and review of literature].

Deng XL, Yin F, Zhang CL, Ma YP, He F, Wu LW, Peng J. Deng XL, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2016 Nov 2;54(11):856-859. doi: 10.3760/cma.j.issn.0578-1310.2016.11.014. Zhonghua Er Ke Za Zhi. 2016. PMID: 27806796 Review. Chinese.

6

[A novel mutation in KCNB1 gene in a child with neuropsychiatric comorbidities with both intellectual disability and epilepsy and review of literature].

Miao P, Peng J, Chen C, Gai N, Yin F. Miao P, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2017 Feb 2;55(2):115-119. doi: 10.3760/cma.j.issn.0578-1310.2017.02.012. Zhonghua Er Ke Za Zhi. 2017. PMID: 28173649 Review. Chinese.

7

[A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].

Zhang CL, Yin F, He F, Gai N, Shi ZQ, Peng J. Zhang CL, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):288-293. doi: 10.3760/cma.j.issn.0578-1310.2017.04.011. Zhonghua Er Ke Za Zhi. 2017. PMID: 28441826 Review. Chinese.

8

[Interpretation of clinical and laboratory interpretation of mitochondrial messenger RNA variants].

Yin F, Wong LJ, Jiang L, Zhou SZ, Fang F, Chen YH, Zhang AH, Cao DZ, Han YL, Sun D, Yang L, Wu TH, Zhang W, Peng J. Yin F, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2021 Dec 2;59(12):1032-1037. doi: 10.3760/cma.j.cn112140-20210611-00498. Zhonghua Er Ke Za Zhi. 2021. PMID: 34856661 Chinese.

9

[DNM1L gene variant caused encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1: three cases report and literature review].

Pan Z, Wu TH, Chen C, Peng P, He YW, Yi WZ, Yin F, Peng J. Pan Z, et al. Among authors: peng j, peng p. Zhonghua Er Ke Za Zhi. 2021 May 2;59(5):400-406. doi: 10.3760/cma.j.cn112140-20200921-00893. Zhonghua Er Ke Za Zhi. 2021. PMID: 33902225 Review. Chinese.

10

[MEGDEL syndrome with an SERAC1 mutation: a case report].

Chen J, Peng J, Yin F. Chen J, et al. Among authors: peng j. Zhonghua Er Ke Za Zhi. 2017 May 4;55(5):394-395. doi: 10.3760/cma.j.issn.0578-1310.2017.05.020. Zhonghua Er Ke Za Zhi. 2017. PMID: 28482397 Chinese. No abstract available.

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