Da Y - Search Results

1

A rare complex structural variant of novel intragenic inversion combined with reciprocal translocation t(X;1)(p21.2;p13.3) in Duchenne muscular dystrophy.

Wang Y, Wen X, Shen XM, Di L, Sun Y, Li Y, Zhang S, Wen Q, Wang J, Duo J, Huang Y, Lu Y, Xu M, Wang M, Chen H, Zhu W, Da Y. Wang Y, et al. Among authors: da y. Neuromuscul Disord. 2024 Jun;39:24-29. doi: 10.1016/j.nmd.2024.04.003. Epub 2024 Apr 12. Neuromuscul Disord. 2024. PMID: 38714145

2

[A study of vascular factor in the pathogenesis of polymyositis].

Wang M, Jia JP, Da YW. Wang M, et al. Zhonghua Nei Ke Za Zhi. 2005 Feb;44(2):115-7. Zhonghua Nei Ke Za Zhi. 2005. PMID: 15840223 Chinese.

3

No association between the promoter polymorphisms of PAI-1 gene and sporadic Alzheimer's disease in Chinese Han population.

Lu Y, Wang M, Liu Z, Wang F, Da Y, Jia J. Lu Y, et al. Among authors: da y. Neurosci Lett. 2009 May 15;455(2):97-100. doi: 10.1016/j.neulet.2009.02.039. Epub 2009 Feb 21. Neurosci Lett. 2009. PMID: 19368854

4

[Detection for trinucleotide repeats in myotonic dystrophy type 1].

Li Y, Da YW. Li Y, et al. Among authors: da yw. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Feb;29(1):16-8. doi: 10.3760/cma.j.issn.1003-9406.2012.01.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22311484 Chinese.

5

Telbivudine myopathy in a patient with chronic hepatitis B.

Wang M, Da Y, Cai H, Lu Y, Wu L, Jia J. Wang M, et al. Among authors: da y. Int J Clin Pharm. 2012 Jun;34(3):422-5. doi: 10.1007/s11096-012-9633-3. Epub 2012 Apr 17. Int J Clin Pharm. 2012. PMID: 22527478

6

A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1.

Lu Y, Li X, Wang M, Li X, Zhang F, Li Y, Zhang M, Da Y, Yu J, Jia J. Lu Y, et al. Among authors: da y. PLoS One. 2012;7(6):e39288. doi: 10.1371/journal.pone.0039288. Epub 2012 Jun 18. PLoS One. 2012. PMID: 22723986 Free PMC article.

7

Giant axonal neuropathy caused by a novel compound heterozygous mutation in the gigaxonin gene.

Xu M, Da YW, Liu L, Wang F, Jia JP. Xu M, et al. J Child Neurol. 2013 Oct;28(10):1316-9. doi: 10.1177/0883073812467688. Epub 2012 Dec 17. J Child Neurol. 2013. PMID: 23248352

8

An unusual case with myotonia.

Da YW, Wang M, Li Y, Lu Y, Jia JP. Da YW, et al. Kaohsiung J Med Sci. 2013 Mar;29(3):172-5. doi: 10.1016/j.kjms.2012.08.029. Epub 2012 Nov 22. Kaohsiung J Med Sci. 2013. PMID: 23465422 Free article.

9

[Clinical and imaging features and genetic analysis of a case with adult-onset Krabbe disease].

Da YW, Li Y, Zhang XQ, Jia JP. Da YW, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Oct;30(5):585-8. doi: 10.3760/cma.j.issn.1003-9406.2013.05.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 24078576 Chinese.

10

Novel RYR1 missense mutations in six Chinese patients with central core disease.

Gu M, Zhang S, Hu J, Yuan Y, Wang Z, Da Y, Wu S. Gu M, et al. Among authors: da y. Neurosci Lett. 2014 Apr 30;566:32-5. doi: 10.1016/j.neulet.2014.02.015. Epub 2014 Feb 20. Neurosci Lett. 2014. PMID: 24561095

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