Da YW - Search Results

1

Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis.

Lei L, Shen XM, Wang SY, Lu Y, Wang SB, Chen H, Liu Z, Ouyang YS, Duo JY, Da YW, Chen ZG. Lei L, et al. Among authors: da yw. Chin Med J (Engl). 2019 Jun 20;132(12):1487-1489. doi: 10.1097/CM9.0000000000000284. Chin Med J (Engl). 2019. PMID: 31205110 Free PMC article.

2

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. 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

3

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. 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

4

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. PLoS One. 2012;7(6):e39288. doi: 10.1371/journal.pone.0039288. Epub 2012 Jun 18. PLoS One. 2012. PMID: 22723986 Free PMC article.

5

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.

6

Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation.

Di L, Chen H, Da Y, Wang S, Shen XM. Di L, et al. J Neurol. 2016 Feb;263(2):263-268. doi: 10.1007/s00415-015-7965-3. Epub 2015 Nov 14. J Neurol. 2016. PMID: 26566915

7

Aberrant trafficking of a Leu89Pro connexin32 mutant associated with X-linked dominant Charcot-Marie-Tooth disease.

Da Y, Wang W, Liu Z, Chen H, Di L, Previch L, Chen Z. Da Y, et al. Neurol Res. 2016 Oct;38(10):897-902. doi: 10.1080/01616412.2016.1204494. Epub 2016 Jul 1. Neurol Res. 2016. PMID: 27367520

8

Successful treatment of periodic paralysis with coenzyme Q10: two case reports.

Da Y, Lei L, Jurkat-Rott K, Lehmann-Horn F. Da Y, et al. Acta Myol. 2016 Oct;35(2):107-108. Acta Myol. 2016. PMID: 28344441 Free PMC article.

9

A unique case of dysferlinopathy with a large-segment duplication mutation who experienced rapid deterioration after small-dosage corticosteroid treatment.

Di L, Guan Y, Shen XM, Da Y. Di L, et al. J Neurol Sci. 2017 May 15;376:35-37. doi: 10.1016/j.jns.2017.02.059. Epub 2017 Feb 27. J Neurol Sci. 2017. PMID: 28431623 No abstract available.

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. 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

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

60 results

Search Page

Filters