Ding C - Search Results

1

Genotype-phenotype correlation of CACNA1A variants in children with epilepsy.

Niu X, Yang Y, Chen Y, Cheng M, Liu M, Ding C, Tian X, Yang Z, Jiang Y, Zhang Y. Niu X, et al. Among authors: ding c. Dev Med Child Neurol. 2022 Jan;64(1):105-111. doi: 10.1111/dmcn.14985. Epub 2021 Jul 15. Dev Med Child Neurol. 2022. PMID: 34263451 Free article.

2

Effectiveness of the first antiepileptic drug in the treatment of pediatric epilepsy.

Ma MS, Ding YX, Ying W, Fang F, Ding CH, Zou LP. Ma MS, et al. Pediatr Neurol. 2009 Jul;41(1):22-6. doi: 10.1016/j.pediatrneurol.2009.01.010. Pediatr Neurol. 2009. PMID: 19520269

3

Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC).

Wang J, Shang J, Wu Y, Gu Q, Xiong H, Ding C, Wang L, Gao Z, Wu X, Jiang Y. Wang J, et al. Among authors: ding c. J Hum Genet. 2011 Feb;56(2):138-42. doi: 10.1038/jhg.2010.146. Epub 2010 Dec 16. J Hum Genet. 2011. PMID: 21160490

4

[Clinical and genetic characteristics of children with Leigh syndrome].

Fang F, Shen Y, Shen DM, Liu ZM, Ding CH, Zhang WC, Sun SZ, Lyu JL, Han TL, Wang XH, Zhang WH, Yang XY, Li JW, Wu HS. Fang F, et al. Among authors: ding ch. Zhonghua Er Ke Za Zhi. 2017 Mar 2;55(3):205-209. doi: 10.3760/cma.j.issn.0578-1310.2017.03.008. Zhonghua Er Ke Za Zhi. 2017. PMID: 28273704 Chinese.

5

[Progressive cavitating leukoencephalopathy: four cases and literatures review].

Ren CH, Fang F, Cheng H, Ding CH, Chen CH, Zhang YJ, Shen DM. Ren CH, et al. Among authors: ding ch. Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):283-287. doi: 10.3760/cma.j.issn.0578-1310.2017.04.010. Zhonghua Er Ke Za Zhi. 2017. PMID: 28441825 Review. Chinese.

6

The clinical and genetic characteristics in children with mitochondrial disease in China.

Fang F, Liu Z, Fang H, Wu J, Shen D, Sun S, Ding C, Han T, Wu Y, Lv J, Yang L, Li S, Lv J, Shen Y. Fang F, et al. Among authors: ding c. Sci China Life Sci. 2017 Jul;60(7):746-757. doi: 10.1007/s11427-017-9080-y. Epub 2017 Jun 16. Sci China Life Sci. 2017. PMID: 28639102

7

[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: ding ch. 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.

8

Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies.

Hernandez CC, XiangWei W, Hu N, Shen D, Shen W, Lagrange AH, Zhang Y, Dai L, Ding C, Sun Z, Hu J, Zhu H, Jiang Y, Macdonald RL. Hernandez CC, et al. Among authors: ding c. Brain. 2019 Jul 1;142(7):1938-1954. doi: 10.1093/brain/awz123. Brain. 2019. PMID: 31056671 Free PMC article.

9

[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. Among authors: ding ch. 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.

10

[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: ding ch. 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.

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