Liang XY - Search Results

1

[Dynamic investigation of nutritional risk in patients with malignant tumor during hospitalization].

Zhu MW, Wei JM, Chen W, Yang X, Cui HY, Zhu SN, Zhang PP, Xiong J, Zheng DF, Song HJ, Liang XY, Zhang L, Xu WY, Wang HB, Su GQ, Feng LJ, Chen T, Wu YD, Li H, Sun JQ, Shi Y, Tong BD, Zhou SM, Wang XY, Huang YH, Zhang BM, Xu J, Zhang HY, Chang GL, Jia ZY, Chen SF, Hu J, Zhang XW, Wang H, Li ZD, Gao YY, Gui B. Zhu MW, et al. Among authors: liang xy. Zhonghua Yi Xue Za Zhi. 2018 Apr 10;98(14):1093-1098. doi: 10.3760/cma.j.issn.0376-2491.2018.14.009. Zhonghua Yi Xue Za Zhi. 2018. PMID: 29690722 Chinese.

2

The Value of Optical Coherence Tomography Angiography in Pituitary Adenomas.

Tang Y, Liang X, Xu J, Wang K, Jia W. Tang Y, et al. J Integr Neurosci. 2022 Aug 12;21(5):142. doi: 10.31083/j.jin2105142. J Integr Neurosci. 2022. PMID: 36137972 Free article.

3

Novel RPE65 mutations associated with Leber congenital amaurosis in Chinese patients.

Xu F, Dong Q, Liu L, Li H, Liang X, Jiang R, Sui R, Dong F. Xu F, et al. Mol Vis. 2012;18:744-50. Epub 2012 Mar 28. Mol Vis. 2012. PMID: 22509104 Free PMC article.

4

Novel CNGA3 mutations in Chinese patients with achromatopsia.

Liang X, Dong F, Li H, Li H, Yang L, Sui R. Liang X, et al. Br J Ophthalmol. 2015 Apr;99(4):571-6. doi: 10.1136/bjophthalmol-2014-305432. Epub 2015 Jan 30. Br J Ophthalmol. 2015. PMID: 25637600

5

The difference of the retinal structural and microvascular characteristics in patients with MOGAD-ON and AQP4-ON.

Yao Y, Li X, Xu Y, Liang X, Yang L, Shi FD, Zhang X, Tian DC, Zhang X. Yao Y, et al. BMC Neurol. 2022 Aug 27;22(1):323. doi: 10.1186/s12883-022-02848-2. BMC Neurol. 2022. PMID: 36030231 Free PMC article.

6

Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.

Jiang L, Liang X, Li Y, Wang J, Zaneveld JE, Wang H, Xu S, Wang K, Wang B, Chen R, Sui R. Jiang L, et al. Orphanet J Rare Dis. 2015 Sep 4;10:110. doi: 10.1186/s13023-015-0329-3. Orphanet J Rare Dis. 2015. PMID: 26338283 Free PMC article.

7

Novel PRPF31 mutations associated with Chinese autosomal dominant retinitis pigmentosa patients.

Xu F, Sui R, Liang X, Li H, Jiang R, Dong F. Xu F, et al. Mol Vis. 2012;18:3021-xxx. Epub 2012 Dec 14. Mol Vis. 2012. PMID: 23288994 Free PMC article.

8

Novel ALMS1 mutations in Chinese patients with Alström syndrome.

Liang X, Li H, Li H, Xu F, Dong F, Sui R. Liang X, et al. Mol Vis. 2013 Sep 7;19:1885-91. eCollection 2013. Mol Vis. 2013. PMID: 24049434 Free PMC article.

9

De novo mutations in the cone-rod homeobox gene associated with leber congenital amaurosis in Chinese patients.

Zou X, Yao F, Liang X, Xu F, Li H, Sui R, Dong F. Zou X, et al. Ophthalmic Genet. 2015 Mar;36(1):21-6. doi: 10.3109/13816810.2013.827219. Epub 2013 Sep 3. Ophthalmic Genet. 2015. PMID: 24001014

10

Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders.

Luo S, Wang PY, Zhou P, Zhang WJ, Gu YJ, Liang XY, Zhang JW, Luo JX, Zhang HW, Lan S, Zhang TT, Yang JH, Sun SZ, Guo XY, Wang JL, Deng LF, Xu ZH, Jin L, He YY, Ye ZL, Gu WY, Li BM, Shi YW, Liu XR, Yan HJ, Yi YH, Jiang YW, Mao X, Li WL, Meng H, Liao WP. Luo S, et al. Among authors: liang xy. Am J Hum Genet. 2025 Jan 2;112(1):87-105. doi: 10.1016/j.ajhg.2024.11.010. Epub 2024 Dec 20. Am J Hum Genet. 2025. PMID: 39708813

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