Gao Z - Search Results

1

A complex intragenic rearrangement of ERCC8 in Chinese siblings with Cockayne syndrome.

Xie H, Li X, Peng J, Chen Q, Gao Z, Song X, Li W, Xiao J, Li C, Zhang T, Gusella JF, Zhong J, Chen X. Xie H, et al. Among authors: gao z. Sci Rep. 2017 Mar 23;7:44271. doi: 10.1038/srep44271. Sci Rep. 2017. PMID: 28333167 Free PMC article.

2

[Emotional and behavioral comorbidities and the impact on the quality of life in epilepsy children].

Chen Q, Yan XX, Shang NX, Zhang GZ, Gao ZJ, Wang Y, Li EZ, Yang J, Xu KM. Chen Q, et al. Zhonghua Er Ke Za Zhi. 2010 May;48(5):346-50. Zhonghua Er Ke Za Zhi. 2010. PMID: 20654034 Chinese.

3

Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion.

Li Q, Zhang Z, Yan Y, Xiao P, Gao Z, Cheng W, Su L, Yu K, Xie H, Chen X, Jiang Q, Li L. Li Q, et al. Among authors: gao z. Mol Cytogenet. 2015 Dec 15;8:95. doi: 10.1186/s13039-015-0201-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 26673557 Free PMC article.

4

[Cognitive profile of children with newly onset benign epilepsy with centro-temporal spikes before treatment:a study of computerized cognitive testing in epilepsy].

Chen Q, Cheng D, Zheng T, Gao Z, Zhang G, Yan X, Zhou X, Luo G, Xu K. Chen Q, et al. Among authors: gao z. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):754-9. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758111 Chinese.

5

Neurocognitive Profiles in Childhood Absence Epilepsy.

Cheng D, Yan X, Gao Z, Xu K, Zhou X, Chen Q. Cheng D, et al. Among authors: gao z. J Child Neurol. 2017 Jan;32(1):46-52. doi: 10.1177/0883073816668465. Epub 2016 Sep 29. J Child Neurol. 2017. PMID: 27664195

6

[Application of single nucleotide polymorphism-microarray and target gene sequencing in the study of genetic etiology of children with unexplained intellectual disability or developmental delay].

Gao ZJ, Jiang Q, Cheng DZ, Yan XX, Chen Q, Xu KM. Gao ZJ, et al. Zhonghua Er Ke Za Zhi. 2016 Oct 2;54(10):740-745. doi: 10.3760/cma.j.issn.0578-1310.2016.10.006. Zhonghua Er Ke Za Zhi. 2016. PMID: 27784475 Chinese.

7

[Clinical and molecular genetic study of nonketotic hyperglycinemia in a Chinese family].

Gao ZJ, Jiang Q, Chen Q, Xu KM. Gao ZJ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Mar;19(3):268-271. doi: 10.7499/j.issn.1008-8830.2017.03.003. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28302194 Free PMC article. Chinese.

8

Common and Distinctive Patterns of Cognitive Dysfunction in Children With Benign Epilepsy Syndromes.

Cheng D, Yan X, Gao Z, Xu K, Zhou X, Chen Q. Cheng D, et al. Among authors: gao z. Pediatr Neurol. 2017 Jul;72:36-41.e1. doi: 10.1016/j.pediatrneurol.2016.12.005. Epub 2017 Jan 4. Pediatr Neurol. 2017. PMID: 28533141

9

Attention Contributes to Arithmetic Deficits in New-Onset Childhood Absence Epilepsy.

Cheng D, Yan X, Gao Z, Xu K, Chen Q. Cheng D, et al. Among authors: gao z. Front Psychiatry. 2017 Sep 14;8:166. doi: 10.3389/fpsyt.2017.00166. eCollection 2017. Front Psychiatry. 2017. PMID: 28959217 Free PMC article.

10

[Clinical manifestation and gene analyses of 15 patients with intellectual disability or developmental delay complicated with congenital nystagmus].

Gao ZJ, Jiang Q, Chen Q, Xu KM, Liu ZQ, Chen XB, Chen XL. Gao ZJ, et al. Zhonghua Er Ke Za Zhi. 2017 Nov 2;55(11):824-829. doi: 10.3760/cma.j.issn.0578-1310.2017.11.007. Zhonghua Er Ke Za Zhi. 2017. PMID: 29141312 Chinese.

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