Bai L - Search Results

1

Optic Nerve Sheath Fenestration for Progressive Visual Loss in Cerebral Venous Sinus Thrombosis: A Long-Term Retrospective Observational Study.

Li Z, Cheng L, Xu Y, Sun Q, Zhang J, Bai L, Feng T, Tan S, Wang H, Deng B, Li Q, Gui Y, Chen H. Li Z, et al. Among authors: bai l. Neurol Ther. 2023 Apr;12(2):441-457. doi: 10.1007/s40120-022-00434-9. Epub 2023 Jan 7. Neurol Ther. 2023. PMID: 36609961 Free PMC article.

2

Genetic Variations of NLR family genes in Behcet's Disease.

Li L, Yu H, Jiang Y, Deng B, Bai L, Kijlstra A, Yang P. Li L, et al. Among authors: bai l. Sci Rep. 2016 Feb 1;6:20098. doi: 10.1038/srep20098. Sci Rep. 2016. PMID: 26833430 Free PMC article. Clinical Trial.

3

Corrigendum: Genetic Variations of NLR family genes in Behcet's Disease.

Li L, Yu H, Jiang Y, Deng B, Bai L, Kijlstra A, Yang P. Li L, et al. Among authors: bai l. Sci Rep. 2016 May 31;6:26423. doi: 10.1038/srep26423. Sci Rep. 2016. PMID: 27241066 Free PMC article. No abstract available.

4

Decreased interleukin-37 expression in Vogt-Koyanagi-Harada disease and upregulation following immunosuppressive treatment.

Ye Z, Wang C, Tang J, Zhou Y, Bai L, Liu Y, Kijlstra A, Yang P. Ye Z, et al. Among authors: bai l. J Interferon Cytokine Res. 2015 Apr;35(4):265-72. doi: 10.1089/jir.2014.0042. Epub 2014 Oct 24. J Interferon Cytokine Res. 2015. PMID: 25343528

5

Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182.

Yu H, Liu Y, Bai L, Kijlstra A, Yang P. Yu H, et al. Among authors: bai l. J Mol Med (Berl). 2014 Sep;92(9):961-7. doi: 10.1007/s00109-014-1159-9. Epub 2014 May 8. J Mol Med (Berl). 2014. PMID: 24801147

6

Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis.

Hou S, Qi J, Liao D, Zhang Q, Fang J, Zhou Y, Liu Y, Bai L, Zhang M, Kijlstra A, Yang P. Hou S, et al. Among authors: bai l. Arthritis Rheum. 2013 Nov;65(11):2963-70. doi: 10.1002/art.38116. Arthritis Rheum. 2013. PMID: 23918728 Free article.

7

Association of T-Bet, GATA-3, RORC, and FOXP3 Copy Number Variations With Acute Anterior Uveitis With or Without Ankylosing Spondylitis in Chinese Han.

Bai L, Liu Y, Hou S, Liao D, Kijlstra A, Yang P. Bai L, et al. Invest Ophthalmol Vis Sci. 2016 Apr;57(4):1847-52. doi: 10.1167/iovs.15-17960. Invest Ophthalmol Vis Sci. 2016. PMID: 27082299

8

miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet's disease.

Hou S, Ye Z, Liao D, Bai L, Liu Y, Zhang J, Kijlstra A, Yang P. Hou S, et al. Among authors: bai l. Sci Rep. 2016 Jan 28;6:20057. doi: 10.1038/srep20057. Sci Rep. 2016. PMID: 26818976 Free PMC article.

9

TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study.

Xiang Q, Chen L, Hou S, Fang J, Zhou Y, Bai L, Liu Y, Kijlstra A, Yang P. Xiang Q, et al. Among authors: bai l. PLoS One. 2014 Jan 8;9(1):e84214. doi: 10.1371/journal.pone.0084214. eCollection 2014. PLoS One. 2014. PMID: 24416204 Free PMC article.

10

Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome.

Li X, Bai L, Fang J, Hou S, Zhou Q, Yu H, Kijlstra A, Yang P. Li X, et al. Among authors: bai l. PLoS One. 2014 May 23;9(5):e98373. doi: 10.1371/journal.pone.0098373. eCollection 2014. PLoS One. 2014. PMID: 24859272 Free PMC article. Clinical Trial.

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