Dai Y - Search Results

1

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: dai y. Front Neurol. 2020 Sep 30;11:572006. doi: 10.3389/fneur.2020.572006. eCollection 2020. Front Neurol. 2020. PMID: 33101180 Free PMC article.

2

Mutational analysis of ATP7B in north Chinese patients with Wilson disease.

Li K, Zhang WM, Lin S, Wen L, Wang ZF, Xie D, Wei M, Qiu ZQ, Dai Y, Lin MC, Kung HF, Yao FX. Li K, et al. Among authors: dai y. J Hum Genet. 2013 Feb;58(2):67-72. doi: 10.1038/jhg.2012.134. Epub 2012 Dec 13. J Hum Genet. 2013. PMID: 23235335

3

Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study.

Wei X, Dai Y, Yu P, Qu N, Lan Z, Hong X, Sun Y, Yang G, Xie S, Shi Q, Zhou H, Zhu Q, Chu Y, Yao F, Wang J, He J, Yang Y, Liang Y, Yang Y, Qi M, Yang L, Wang W, Wu H, Duan J, Shen C, Wang J, Cui L, Yi X. Wei X, et al. Among authors: dai y. Eur J Hum Genet. 2014 Jan;22(1):110-8. doi: 10.1038/ejhg.2013.82. Epub 2013 Jun 12. Eur J Hum Genet. 2014. PMID: 23756440 Free PMC article.

4

A novel dystrophin deletion mutation in a becker muscular dystrophy patient with early-onset dilated cardiomyopathy.

Guo X, Dai Y, Cui L, Fang Q. Guo X, et al. Among authors: dai y. Can J Cardiol. 2014 Aug;30(8):956.e1-3. doi: 10.1016/j.cjca.2014.05.002. Epub 2014 May 6. Can J Cardiol. 2014. PMID: 24996370

5

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

6

Targeted next generation sequencing identifies two novel mutations in SEPN1 in rigid spine muscular dystrophy 1.

Dai Y, Liang S, Huang Y, Chen L, Banerjee S. Dai Y, et al. Oncotarget. 2016 Dec 20;7(51):83843-83849. doi: 10.18632/oncotarget.13337. Oncotarget. 2016. PMID: 27863379 Free PMC article.

7

An LMNB1 Duplication Caused Adult-Onset Autosomal Dominant Leukodystrophy in Chinese Family: Clinical Manifestations, Neuroradiology and Genetic Diagnosis.

Dai Y, Ma Y, Li S, Banerjee S, Liang S, Liu Q, Yang Y, Peng B, Cui L, Jin L. Dai Y, et al. Front Mol Neurosci. 2017 Jul 18;10:215. doi: 10.3389/fnmol.2017.00215. eCollection 2017. Front Mol Neurosci. 2017. PMID: 28769756 Free PMC article.

8

A Novel AGRN Mutation Leads to Congenital Myasthenic Syndrome Only Affecting Limb-girdle Muscle.

Zhang Y, Dai Y, Han JN, Chen ZH, Ling L, Pu CQ, Cui LY, Huang XS. Zhang Y, et al. Among authors: dai y. Chin Med J (Engl). 2017 Oct 5;130(19):2279-2282. doi: 10.4103/0366-6999.215332. Chin Med J (Engl). 2017. PMID: 28937031 Free PMC article.

9

Mechanism hypotheses for the electrophysiological manifestations of two cases of endplate acetylcholinesterase deficiency related congenital myasthenic syndrome.

Ding Q, Shen D, Dai Y, Hu Y, Guan Y, Liu M, Cui L. Ding Q, et al. Among authors: dai y. J Clin Neurosci. 2018 Feb;48:229-232. doi: 10.1016/j.jocn.2017.10.084. Epub 2017 Nov 14. J Clin Neurosci. 2018. PMID: 29150079

10

Comparison of myelin oligodendrocyte glycoprotein (MOG)-antibody disease and AQP4-IgG-positive neuromyelitis optica spectrum disorder (NMOSD) when they co-exist with anti-NMDA (N-methyl-D-aspartate) receptor encephalitis.

Fan S, Xu Y, Ren H, Guan H, Feng F, Gao X, Ding D, Fang F, Shan G, Guan T, Zhang Y, Dai Y, Yao M, Peng B, Zhu Y, Cui L. Fan S, et al. Among authors: dai y. Mult Scler Relat Disord. 2018 Feb;20:144-152. doi: 10.1016/j.msard.2018.01.007. Epub 2018 Jan 31. Mult Scler Relat Disord. 2018. PMID: 29414288 Review.

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