Dai Y - Search Results

1

Comparison of neurofilament light and heavy chain in spinal muscular atrophy and amyotrophic lateral sclerosis: A pilot study.

Li JY, Dai Y, Sun XH, Ren HT, Shen DC, Yang XZ, Liu MS, Cui LY. Li JY, et al. Among authors: dai y. Brain Behav. 2023 May;13(5):e2997. doi: 10.1002/brb3.2997. Epub 2023 Apr 17. Brain Behav. 2023. PMID: 37070132 Free PMC article.

2

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.

3

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

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

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.

6

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.

7

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

8

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.

9

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.

10

Surgical outcomes in patients with anti-N-methyl D-aspartate receptor encephalitis with ovarian teratoma.

Dai Y, Zhang J, Ren H, Zhou X, Chen J, Cui L, Lang J, Guan H, Sun D. Dai Y, et al. Am J Obstet Gynecol. 2019 Nov;221(5):485.e1-485.e10. doi: 10.1016/j.ajog.2019.05.026. Epub 2019 May 22. Am J Obstet Gynecol. 2019. PMID: 31128109

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