Xi J - Search Results

1

5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy.

Xi J, Wang X, Yue D, Dou T, Wu Q, Lu J, Liu Y, Yu W, Qiao K, Lin J, Luo S, Li J, Du A, Dong J, Chen Y, Luo L, Yang J, Niu Z, Liang Z, Zhao C, Lu J, Zhu W, Zhou Y. Xi J, et al. Brain. 2021 Mar 3;144(2):601-614. doi: 10.1093/brain/awaa426. Brain. 2021. PMID: 33374016

2

Decrease of CD4(+)CD25(high)Foxp3(+) regulatory T cells and elevation of CD19(+)BAFF-R(+) B cells and soluble ICAM-1 in myasthenia gravis.

Li X, Xiao BG, Xi JY, Lu CZ, Lu JH. Li X, et al. Clin Immunol. 2008 Feb;126(2):180-8. doi: 10.1016/j.clim.2007.10.001. Epub 2007 Nov 28. Clin Immunol. 2008. PMID: 18054287

3

A series of Chinese patients with desminopathy associated with six novel and one reported mutations in the desmin gene.

Hong D, Wang Z, Zhang W, Xi J, Lu J, Luan X, Yuan Y. Hong D, et al. Among authors: xi j. Neuropathol Appl Neurobiol. 2011 Apr;37(3):257-70. doi: 10.1111/j.1365-2990.2010.01112.x. Neuropathol Appl Neurobiol. 2011. PMID: 20696008

4

Clinical and pathological features in 15 Chinese patients with calpainopathy.

Luo SS, Xi JY, Lu JH, Zhao CB, Zhu WH, Lin J, Wang Y, Ren HM, Yin B, Andoni UJ. Luo SS, et al. Among authors: xi jy. Muscle Nerve. 2011 Mar;43(3):402-9. doi: 10.1002/mus.21908. Epub 2010 Dec 9. Muscle Nerve. 2011. PMID: 21321956

5

HLA-DQA1*03:02/DQB1*03:03:02 is strongly associated with susceptibility to childhood-onset ocular myasthenia gravis in Southern Han Chinese.

Zhu WH, Lu JH, Lin J, Xi JY, Lu J, Luo SS, Qiao K, Xiao BG, Lu CZ, Zhao CB. Zhu WH, et al. Among authors: xi jy. J Neuroimmunol. 2012 Jun 15;247(1-2):81-5. doi: 10.1016/j.jneuroim.2012.03.018. Epub 2012 Apr 13. J Neuroimmunol. 2012. PMID: 22503410

6

Genetic variability and clinical spectrum of Chinese patients with limb-girdle muscular dystrophy type 2A.

Luo SS, Xi JY, Zhu WH, Zhao CB, Lu JH, Lin J, Wang Y, Lu J, Qiao K. Luo SS, et al. Among authors: xi jy. Muscle Nerve. 2012 Nov;46(5):723-9. doi: 10.1002/mus.23381. Epub 2012 Aug 24. Muscle Nerve. 2012. PMID: 22926650

7

Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS.

Lin J, Zhao CB, Lu JH, Wang HJ, Zhu WH, Xi JY, Lu J, Luo SS, Ma D, Wang Y, Xiao BG, Lu CZ. Lin J, et al. Among authors: xi jy. Mitochondrial DNA. 2014 Feb;25(1):56-62. doi: 10.3109/19401736.2013.779259. Epub 2013 Jul 8. Mitochondrial DNA. 2014. PMID: 23834081

8

Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Xi J, Wen B, Lin J, Zhu W, Luo S, Zhao C, Li D, Lin P, Lu J, Yan C. Xi J, et al. J Inherit Metab Dis. 2014 May;37(3):399-404. doi: 10.1007/s10545-013-9671-6. Epub 2013 Dec 20. J Inherit Metab Dis. 2014. PMID: 24357026

9

Novel LAMP2 mutations in Chinese patients with Danon disease cause varying degrees of clinical severity.

Luo SS, Xi JY, Cai S, Zhao CB, Lu JH, Zhu WH, Lin J, Qiao K, Wang Y, Ye ZR. Luo SS, et al. Among authors: xi jy. Clin Neuropathol. 2014 Jul-Aug;33(4):284-91. doi: 10.5414/NP300668. Clin Neuropathol. 2014. PMID: 24691104

10

Multiple deep white matter lesions mimic multiple sclerosis as an unusual complication of left atrial myxoma.

Quan C, ZhangBao J, Luo S, Fang K, Xi J, Du Z, Zhao C, Lu J. Quan C, et al. Among authors: xi j. Mult Scler. 2015 Jan;21(1):108-10. doi: 10.1177/1352458514535677. Epub 2014 May 22. Mult Scler. 2015. PMID: 24852922

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