Da Y - Search Results

1

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

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

Study of antibodies to PMP22, IL-6 and TNF-alpha concentrations in serum in a CMTX1 family.

Da Y, Jia J. Da Y, et al. Neurosci Lett. 2007 Sep 7;424(2):73-7. doi: 10.1016/j.neulet.2007.06.051. Epub 2007 Aug 3. Neurosci Lett. 2007. PMID: 17714866

4

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

5

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.

6

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

7

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.

8

Posterior reversible encephalopathy syndrome in a leber hereditary optic neuropathy patient with mitochondrial DNA 11778G>A point mutation.

Da Y, Zhang X, Li F, Yang X, Zhang X, Jia J. Da Y, et al. J Neuroophthalmol. 2013 Sep;33(3):276-8. doi: 10.1097/WNO.0b013e31828f8d75. J Neuroophthalmol. 2013. PMID: 23782927

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

Monoclonal gammopathy with both nemaline myopathy and amyloid myopathy.

Wang M, Lei L, Chen H, Di L, Pang M, Lu Y, Lu L, Shen XM, Da Y. Wang M, et al. Among authors: da y. Neuromuscul Disord. 2017 Oct;27(10):942-946. doi: 10.1016/j.nmd.2017.05.007. Epub 2017 May 11. Neuromuscul Disord. 2017. PMID: 28606401

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