Yang XZ - Search Results

1

[Research on applying genetic and environmental risk score in risk-adapted colorectal cancer screening].

Luo CY, Zhang YH, Lu M, Lu B, Cai J, Li N, Zhou YY, Luo JH, Zhang DD, Yang XZ, Chen HD, Dai M. Luo CY, et al. Among authors: yang xz. Zhonghua Liu Xing Bing Xue Za Zhi. 2023 Jun 10;44(6):999-1005. doi: 10.3760/cma.j.cn112338-20221102-00935. Zhonghua Liu Xing Bing Xue Za Zhi. 2023. PMID: 37380425 Clinical Trial. Chinese.

2

[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].

Yang X, Zhang Y, Xu X, Wang S, Yang Z, Wu Y, Zhang X, Liu X, Wu X. Yang X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):679-85. doi: 10.3760/cma.j.issn.1003-9406.2014.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449067 Chinese.

3

[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy].

Yang X, Zhang Y, Xu X, Yu X, Zhang X, Yang Z, Wang S, Wu Y, Liu X, Wu X. Yang X, et al. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):806-11. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582463 Chinese.

4

[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome].

Zeng Q, Zhang Y, Yang X, Xu X, Zhang J, Tian X, Liu A, Liu X, Jiang Y, Wu X. Zeng Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):787-791. doi: 10.3760/cma.j.issn.1003-9406.2017.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188601 Chinese.

5

[Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders].

Qian P, Yang X, Xu X, Liu X, Zhang Y, Yang Z. Qian P, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):314-318. doi: 10.3760/cma.j.issn.1003-9406.2018.03.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896722 Chinese.

6

Phenotypes of GNAO1 Variants in a Chinese Cohort.

Yang X, Niu X, Yang Y, Cheng M, Zhang J, Chen J, Yang Z, Zhang Y. Yang X, et al. Front Neurol. 2021 May 28;12:662162. doi: 10.3389/fneur.2021.662162. eCollection 2021. Front Neurol. 2021. PMID: 34122306 Free PMC article.

7

DYNC1H1-related epilepsy: Genotype-phenotype correlation.

Liu W, Cheng M, Zhu Y, Chen Y, Yang Y, Chen H, Niu X, Tian X, Yang X, Zhang Y. Liu W, et al. Dev Med Child Neurol. 2023 Apr;65(4):534-543. doi: 10.1111/dmcn.15414. Epub 2022 Sep 29. Dev Med Child Neurol. 2023. PMID: 36175372 Free article.

8

Osimertinib versus comparator first-generation epidermal growth factor receptor tyrosine kinase inhibitors as first-line treatment in patients with advanced EGFR-mutated non-small cell lung cancer: a Chinese, multicenter, real-world cohort study.

Zhang D, Liu X, Shen F, Zhao D, Shi Y, Zhang H, Liu J, Gao X, Chen M, Zhao J, Zhong W, Gao J, He M, Liu Y, Yang X, Qin J, Tang Y, Mu X, Gu Y, Zhang S, Chen X, Pang L, Meng Q, Guo Y, Zhang Y, Li W, Xing P, Cheng Y, Xin T, Li Q, Li Y, Chen J, Gao F, Jin B, Rossi A, Adachi H, Guerrera F, Husain H, Xu Y, Wang M. Zhang D, et al. Transl Lung Cancer Res. 2023 Nov 30;12(11):2229-2244. doi: 10.21037/tlcr-23-577. Epub 2023 Oct 26. Transl Lung Cancer Res. 2023. PMID: 38090527 Free PMC article.

9

Clinical diagnosis, treatment, and ALDH7A1 mutations in pyridoxine-dependent epilepsy in three Chinese infants.

Yang Z, Yang X, Wu Y, Wang J, Zhang Y, Xiong H, Jiang Y, Qin J. Yang Z, et al. PLoS One. 2014 Mar 24;9(3):e92803. doi: 10.1371/journal.pone.0092803. eCollection 2014. PLoS One. 2014. PMID: 24664145 Free PMC article. Clinical Trial.

10

ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients.

Yang X, Gao H, Zhang J, Xu X, Liu X, Wu X, Wei L, Zhang Y. Yang X, et al. PLoS One. 2014 May 19;9(5):e97274. doi: 10.1371/journal.pone.0097274. eCollection 2014. PLoS One. 2014. PMID: 24842602 Free PMC article.

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