Zhao YH - Search Results

1

[Clinical features and genetic diagnosis of Kennedy disease].

Xie MQ, Li XG, Cui LY, Liu MS, Li BH, Zhao YH. Xie MQ, et al. Among authors: zhao yh. Zhonghua Yi Xue Za Zhi. 2010 Sep 21;90(35):2498-500. Zhonghua Yi Xue Za Zhi. 2010. PMID: 21092480 Chinese.

2

[Clinical and pathological features of glycogen storage disease type III].

Dai YJ, Chen L, Guo YP, Ren HT, Zhao YH, Wei M, Qiu ZQ, Song HM. Dai YJ, et al. Among authors: zhao yh. Zhonghua Yi Xue Za Zhi. 2009 Apr 21;89(15):1064-6. Zhonghua Yi Xue Za Zhi. 2009. PMID: 19595259 Chinese.

3

Association between DPP6 polymorphism and the risk of sporadic amyotrophic lateral sclerosis in Chinese patients.

Li XG, Zhang JH, Xie MQ, Liu MS, Li BH, Zhao YH, Ren HT, Cui LY. Li XG, et al. Among authors: zhao yh. Chin Med J (Engl). 2009 Dec 20;122(24):2989-92. Chin Med J (Engl). 2009. PMID: 20137488

4

A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencing.

Dai Y, Wei X, Zhao Y, Ren H, Lan Z, Yang Y, Chen L, Cui L. Dai Y, et al. Neuromuscul Disord. 2015 Aug;25(8):617-24. doi: 10.1016/j.nmd.2015.03.002. Epub 2015 Mar 17. Neuromuscul Disord. 2015. PMID: 25987458

5

Detection of virus in CSF from the cases with meningoencephalitis by next-generation sequencing.

Guan H, Shen A, Lv X, Yang X, Ren H, Zhao Y, Zhang Y, Gong Y, Ni P, Wu H, Zhu Y, Cui L. Guan H, et al. J Neurovirol. 2016 Apr;22(2):240-5. doi: 10.1007/s13365-015-0390-7. Epub 2015 Oct 27. J Neurovirol. 2016. PMID: 26506841

6

[Diagnosis of Muscular Dystrophy Using Western Blot with Micro-sample of Muscle].

Wu DY, Chen L, Zhao YH, Ren HT, Guan HZ, Wei YP, Liu Z, Qian M, Guo YP, Cui LY, Jiao JS. Wu DY, et al. Among authors: zhao yh. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2015 Dec;37(6):705-10. doi: 10.3881/j.issn.1000-503X.2015.06.011. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2015. PMID: 26725394 Chinese.

7

An update on the clinical diagnostic value of β-hCG and αFP for intracranial germ cell tumors.

Hu M, Guan H, Lau CC, Terashima K, Jin Z, Cui L, Wang Y, Li G, Yao Y, Guo Y, Li YM, Zhong D, Xiao J, Wan X, Lian X, Feng F, Ren H, Zhao Y, Cheng X, Gu F. Hu M, et al. Eur J Med Res. 2016 Mar 12;21:10. doi: 10.1186/s40001-016-0204-2. Eur J Med Res. 2016. PMID: 26968839 Free PMC article.

8

Whole exome sequencing identified a novel DAG1 mutation in a patient with rare, mild and late age of onset muscular dystrophy-dystroglycanopathy.

Dai Y, Liang S, Dong X, Zhao Y, Ren H, Guan Y, Yin H, Li C, Chen L, Cui L, Banerjee S. Dai Y, et al. J Cell Mol Med. 2019 Feb;23(2):811-818. doi: 10.1111/jcmm.13979. Epub 2018 Nov 18. J Cell Mol Med. 2019. PMID: 30450679 Free PMC article.

9

A Comprehensive Analysis of 2013 Dystrophinopathies in China: A Report From National Rare Disease Center.

Tong YR, Geng C, Guan YZ, Zhao YH, Ren HT, Yao FX, Ling C, Wang DC, Chen L, Cui LY, Zhang SY, Dai Y. Tong YR, et al. Among authors: zhao yh. Front Neurol. 2020 Sep 30;11:572006. doi: 10.3389/fneur.2020.572006. eCollection 2020. Front Neurol. 2020. PMID: 33101180 Free PMC article.

10

Identification and characterization of two DMD pedigrees with large inversion mutations based on a long-read sequencing pipeline.

Geng C, Zhang C, Li P, Tong Y, Zhu B, He J, Zhao Y, Yao F, Cui LY, Liang F, Wang Y, Wang Y, Jin H, Lang D, Liu S, Wang D, Park MS, Chen L, Peng J, Dai Y. Geng C, et al. Eur J Hum Genet. 2023 May;31(5):504-511. doi: 10.1038/s41431-022-01190-y. Epub 2022 Oct 5. Eur J Hum Genet. 2023. PMID: 36198806 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

923 results

Search Page

Filters