Zhao CB - Search Results

1

Safety of COVID-19 vaccine in patients with myasthenia gravis: a self-controlled case series study.

Ruan Z, Huan X, Su Y, Tang YL, Meng DD, Ren DL, Li CH, Hao SJ, Zhao CB, Luo SS, Li ZY, Chang T. Ruan Z, et al. Among authors: zhao cb. Front Immunol. 2023 May 8;14:1141983. doi: 10.3389/fimmu.2023.1141983. eCollection 2023. Front Immunol. 2023. PMID: 37223097 Free PMC article.

2

Increase of circulating CD4+CD25+ T cells in myasthenia gravis patients with stability and thymectomy.

Sun Y, Qiao J, Lu CZ, Zhao CB, Zhu XM, Xiao BG. Sun Y, et al. Among authors: zhao cb. Clin Immunol. 2004 Sep;112(3):284-9. doi: 10.1016/j.clim.2004.04.005. Clin Immunol. 2004. PMID: 15308122

3

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: zhao cb. Muscle Nerve. 2011 Mar;43(3):402-9. doi: 10.1002/mus.21908. Epub 2010 Dec 9. Muscle Nerve. 2011. PMID: 21321956

4

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: zhao cb. 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

5

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: zhao cb. Muscle Nerve. 2012 Nov;46(5):723-9. doi: 10.1002/mus.23381. Epub 2012 Aug 24. Muscle Nerve. 2012. PMID: 22926650

6

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: zhao cb. Mitochondrial DNA. 2014 Feb;25(1):56-62. doi: 10.3109/19401736.2013.779259. Epub 2013 Jul 8. Mitochondrial DNA. 2014. PMID: 23834081

7

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

8

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. Mult Scler. 2015 Jan;21(1):108-10. doi: 10.1177/1352458514535677. Epub 2014 May 22. Mult Scler. 2015. PMID: 24852922

9

Giant cell polymyositis associated with myasthenia gravis and thymoma.

Lin J, Lu J, Zhao C, Qiao K, Zhu W, Yue D, Luo S, Wang Y, Fang W, Lu J. Lin J, et al. J Clin Neurosci. 2014 Dec;21(12):2252-4. doi: 10.1016/j.jocn.2014.04.027. Epub 2014 Aug 2. J Clin Neurosci. 2014. PMID: 25096712

10

New disease allele and de novo mutation indicate mutational vulnerability of titin exon 343 in hereditary myopathy with early respiratory failure.

Yue D, Gao M, Zhu W, Luo S, Xi J, Wang B, Li Y, Cai S, Li J, Wang Y, Lu J, Zhao C. Yue D, et al. Neuromuscul Disord. 2015 Feb;25(2):172-6. doi: 10.1016/j.nmd.2014.11.005. Epub 2014 Nov 18. Neuromuscul Disord. 2015. PMID: 25500009

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